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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">More severe cellular phenotype in human idiopathic dilated cardiomyopathy compared to ischemic heart disease</title><author><name sortKey="Hamdani, Nazha" sort="Hamdani, Nazha" uniqKey="Hamdani N" first="Nazha" last="Hamdani">Nazha Hamdani</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Borbely, Attila" sort="Borbely, Attila" uniqKey="Borbely A" first="Attila" last="Borbély">Attila Borbély</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Veenstra, Sophie P G R" sort="Veenstra, Sophie P G R" uniqKey="Veenstra S" first="Sophie P. G. R." last="Veenstra">Sophie P. G. R. Veenstra</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Kooij, Viola" sort="Kooij, Viola" uniqKey="Kooij V" first="Viola" last="Kooij">Viola Kooij</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Vrydag, Wim" sort="Vrydag, Wim" uniqKey="Vrydag W" first="Wim" last="Vrydag">Wim Vrydag</name><affiliation><nlm:aff id="Aff4">Department of Pharmacology and Pharmacotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Zaremba, Ruud" sort="Zaremba, Ruud" uniqKey="Zaremba R" first="Ruud" last="Zaremba">Ruud Zaremba</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Dos Remedios, Cris" sort="Dos Remedios, Cris" uniqKey="Dos Remedios C" first="Cris" last="Dos Remedios">Cris Dos Remedios</name><affiliation><nlm:aff id="Aff3">Muscle Research Unit, Institute for Biomedical Research, The University of Sydney, Sydney, Australia</nlm:aff></affiliation></author><author><name sortKey="Niessen, Hans W M" sort="Niessen, Hans W M" uniqKey="Niessen H" first="Hans W. M." last="Niessen">Hans W. M. Niessen</name><affiliation><nlm:aff id="Aff2">Department of Pathology, Institute for Cardiovascular Research, VU University Medical Center Amsterdam, Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Michel, Martin C" sort="Michel, Martin C" uniqKey="Michel M" first="Martin C." last="Michel">Martin C. Michel</name><affiliation><nlm:aff id="Aff4">Department of Pharmacology and Pharmacotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Paulus, Walter J" sort="Paulus, Walter J" uniqKey="Paulus W" first="Walter J." last="Paulus">Walter J. Paulus</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Stienen, Ger J M" sort="Stienen, Ger J M" uniqKey="Stienen G" first="Ger J. M." last="Stienen">Ger J. M. Stienen</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Der Velden, Jolanda" sort="Van Der Velden, Jolanda" uniqKey="Van Der Velden J" first="Jolanda" last="Van Der Velden">Jolanda Van Der Velden</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">21132354</idno><idno type="pmc">3005110</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005110</idno><idno type="RBID">PMC:3005110</idno><idno type="doi">10.1007/s10974-010-9231-8</idno><date when="2010">2010</date><idno type="wicri:Area/Pmc/Corpus">000159</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">More severe cellular phenotype in human idiopathic dilated cardiomyopathy compared to ischemic heart disease</title><author><name sortKey="Hamdani, Nazha" sort="Hamdani, Nazha" uniqKey="Hamdani N" first="Nazha" last="Hamdani">Nazha Hamdani</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Borbely, Attila" sort="Borbely, Attila" uniqKey="Borbely A" first="Attila" last="Borbély">Attila Borbély</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Veenstra, Sophie P G R" sort="Veenstra, Sophie P G R" uniqKey="Veenstra S" first="Sophie P. G. R." last="Veenstra">Sophie P. G. R. Veenstra</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Kooij, Viola" sort="Kooij, Viola" uniqKey="Kooij V" first="Viola" last="Kooij">Viola Kooij</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Vrydag, Wim" sort="Vrydag, Wim" uniqKey="Vrydag W" first="Wim" last="Vrydag">Wim Vrydag</name><affiliation><nlm:aff id="Aff4">Department of Pharmacology and Pharmacotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Zaremba, Ruud" sort="Zaremba, Ruud" uniqKey="Zaremba R" first="Ruud" last="Zaremba">Ruud Zaremba</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Dos Remedios, Cris" sort="Dos Remedios, Cris" uniqKey="Dos Remedios C" first="Cris" last="Dos Remedios">Cris Dos Remedios</name><affiliation><nlm:aff id="Aff3">Muscle Research Unit, Institute for Biomedical Research, The University of Sydney, Sydney, Australia</nlm:aff></affiliation></author><author><name sortKey="Niessen, Hans W M" sort="Niessen, Hans W M" uniqKey="Niessen H" first="Hans W. M." last="Niessen">Hans W. M. Niessen</name><affiliation><nlm:aff id="Aff2">Department of Pathology, Institute for Cardiovascular Research, VU University Medical Center Amsterdam, Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Michel, Martin C" sort="Michel, Martin C" uniqKey="Michel M" first="Martin C." last="Michel">Martin C. Michel</name><affiliation><nlm:aff id="Aff4">Department of Pharmacology and Pharmacotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Paulus, Walter J" sort="Paulus, Walter J" uniqKey="Paulus W" first="Walter J." last="Paulus">Walter J. Paulus</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Stienen, Ger J M" sort="Stienen, Ger J M" uniqKey="Stienen G" first="Ger J. M." last="Stienen">Ger J. M. Stienen</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Der Velden, Jolanda" sort="Van Der Velden, Jolanda" uniqKey="Van Der Velden J" first="Jolanda" last="Van Der Velden">Jolanda Van Der Velden</name><affiliation><nlm:aff id="Aff1">Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</nlm:aff></affiliation></author></analytic><series><title level="j">Journal of Muscle Research and Cell Motility</title><idno type="ISSN">0142-4319</idno><idno type="eISSN">1573-2657</idno><imprint><date when="2010">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Activation of the β-adrenergic receptor (βAR) pathway is the main mechanism of the heart to increase cardiac output via protein kinase A (PKA)-mediated phosphorylation of cellular target proteins, and perturbations therein may contribute to cardiac dysfunction in heart failure. In the present study a comprehensive analysis was made of mediators of the βAR pathway, myofilament properties and cardiac structure in patients with idiopathic (IDCM; n = 13) and ischemic (ISHD; n = 10) cardiomyopathy in comparison to non-failing hearts (donor; n = 10) for the following parameters: βAR density, G-coupled receptor kinases 2 and 5, stimulatory and inhibitory G-proteins, phosphorylation of myofilament targets of PKA, protein phosphatase 1, phospholamban, SERCA2a and single myocyte contractility. All parameters exhibited the expected alterations of heart failure, but for most of them the extent of alteration was greater in IDCM than in ISHD. Histological analysis also revealed higher collagen in IDCM compared to ISHD. Alterations in the βAR pathway are more pronounced in IDCM than in ISHD and may reflect sequential changes in cellular protein composition and function. Our data indicate that cellular dysfunction is more severe in IDCM than in ISHD.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Anversa, P" uniqKey="Anversa P">P Anversa</name></author><author><name sortKey="Ricci, R" uniqKey="Ricci R">R Ricci</name></author><author><name sortKey="Olivetti, G" uniqKey="Olivetti G">G Olivetti</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Arai, M" uniqKey="Arai M">M Arai</name></author><author><name sortKey="Alpert, Nr" uniqKey="Alpert N">NR Alpert</name></author><author><name sortKey="Mac Lennan, Dh" uniqKey="Mac Lennan D">DH Mac Lennan</name></author><author><name sortKey="Barton, P" uniqKey="Barton P">P Barton</name></author><author><name sortKey="Petiasamy, M" uniqKey="Petiasamy M">M Petiasamy</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Bers, Dm" uniqKey="Bers D">DM Bers</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Bohm, M" uniqKey="Bohm M">M Bohm</name></author><author><name sortKey="Maack, C" uniqKey="Maack C">C Maack</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Borbely, A" uniqKey="Borbely A">A Borbély</name></author><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author><author><name sortKey="Papp, Z" uniqKey="Papp Z">Z Papp</name></author><author><name sortKey="Bronzwaer, Jg" uniqKey="Bronzwaer J">JG Bronzwaer</name></author><author><name sortKey="Edes, I" uniqKey="Edes I">I Edes</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author><author><name sortKey="Paulus, Wj" uniqKey="Paulus W">WJ Paulus</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Borbely, A" uniqKey="Borbely A">A Borbély</name></author><author><name sortKey="Falcao Pires, I" uniqKey="Falcao Pires I">I Falcao-Pires</name></author><author><name sortKey="Heerebeek, L" uniqKey="Heerebeek L">L Heerebeek</name></author><author><name sortKey="Hamdani, N" uniqKey="Hamdani N">N Hamdani</name></author><author><name sortKey="Edes, I" uniqKey="Edes I">I Edes</name></author><author><name sortKey="Gavina, C" uniqKey="Gavina C">C Gavina</name></author><author><name sortKey="Leite Moreira, Af" uniqKey="Leite Moreira A">AF Leite-Moreira</name></author><author><name sortKey="Bronzwaer, Jg" uniqKey="Bronzwaer J">JG Bronzwaer</name></author><author><name sortKey="Papp, Z" uniqKey="Papp Z">Z Papp</name></author><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author><author><name sortKey="Paulus, Wj" uniqKey="Paulus W">WJ Paulus</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Brodde, Oe" uniqKey="Brodde O">OE Brodde</name></author><author><name sortKey="Michel, Mc" uniqKey="Michel M">MC Michel</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Carr, An" uniqKey="Carr A">AN Carr</name></author><author><name sortKey="Schmidt, Ag" uniqKey="Schmidt A">AG Schmidt</name></author><author><name sortKey="Suzuki, Y" uniqKey="Suzuki Y">Y Suzuki</name></author><author><name sortKey="Del Monte, F" uniqKey="Del Monte F">F del Monte</name></author><author><name sortKey="Sato, Y" uniqKey="Sato Y">Y Sato</name></author><author><name sortKey="Lanner, C" uniqKey="Lanner C">C Lanner</name></author><author><name sortKey="Breeden, K" uniqKey="Breeden K">K Breeden</name></author><author><name sortKey="Jing, Sl" uniqKey="Jing S">SL Jing</name></author><author><name sortKey="Allen, Pb" uniqKey="Allen P">PB Allen</name></author><author><name sortKey="Greengard, P" uniqKey="Greengard P">P Greengard</name></author><author><name sortKey="Yatani, A" uniqKey="Yatani A">A Yatani</name></author><author><name sortKey="Hoit, Bd" uniqKey="Hoit B">BD Hoit</name></author><author><name sortKey="Grupp, Il" uniqKey="Grupp I">IL Grupp</name></author><author><name sortKey="Hajjar, Rj" uniqKey="Hajjar R">RJ Hajjar</name></author><author><name sortKey="Depaoli Roach, Aa" uniqKey="Depaoli Roach A">AA DePaoli-Roach</name></author><author><name sortKey="Kranias, Eg" uniqKey="Kranias E">EG Kranias</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Cheng, Y" uniqKey="Cheng Y">Y Cheng</name></author><author><name sortKey="Prusoff, Wh" uniqKey="Prusoff W">WH Prusoff</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Cho, H" uniqKey="Cho H">H Cho</name></author><author><name sortKey="Kehrl, Jh" uniqKey="Kehrl J">JH Kehrl</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Cohn, Jn" uniqKey="Cohn J">JN Cohn</name></author><author><name sortKey="Levine, Tb" uniqKey="Levine T">TB Levine</name></author><author><name sortKey="Olivari, Mt" uniqKey="Olivari M">MT Olivari</name></author><author><name sortKey="Garberg, V" uniqKey="Garberg V">V Garberg</name></author><author><name sortKey="Lura, D" uniqKey="Lura D">D Lura</name></author><author><name sortKey="Francis, Gs" uniqKey="Francis G">GS Francis</name></author><author><name sortKey="Simon, Ab" uniqKey="Simon A">AB Simon</name></author><author><name sortKey="Rector, T" uniqKey="Rector T">T Rector</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Copeland, O" uniqKey="Copeland O">O Copeland</name></author><author><name sortKey="Sadayappan, S" uniqKey="Sadayappan S">S Sadayappan</name></author><author><name sortKey="Messer, Ae" uniqKey="Messer A">AE Messer</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author><author><name sortKey="Marston, Sb" uniqKey="Marston S">SB Marston</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="El Armouche, A" uniqKey="El Armouche A">A El-Armouche</name></author><author><name sortKey="Pohlmann, L" uniqKey="Pohlmann L">L Pohlmann</name></author><author><name sortKey="Schlossarek, S" uniqKey="Schlossarek S">S Schlossarek</name></author><author><name sortKey="Starbatty, J" uniqKey="Starbatty J">J Starbatty</name></author><author><name sortKey="Yeh, Yh" uniqKey="Yeh Y">YH Yeh</name></author><author><name sortKey="Nattel, S" uniqKey="Nattel S">S Nattel</name></author><author><name sortKey="Dobrev, D" uniqKey="Dobrev D">D Dobrev</name></author><author><name sortKey="Eschenhagen, T" uniqKey="Eschenhagen T">T Eschenhagen</name></author><author><name sortKey="Carrier, L" uniqKey="Carrier L">L Carrier</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Elliott, P" uniqKey="Elliott P">P Elliott</name></author><author><name sortKey="Andersson, B" uniqKey="Andersson B">B Andersson</name></author><author><name sortKey="Arbustini, E" uniqKey="Arbustini E">E Arbustini</name></author><author><name sortKey="Bilinska, Z" uniqKey="Bilinska Z">Z Bilinska</name></author><author><name sortKey="Cecchi, F" uniqKey="Cecchi F">F Cecchi</name></author><author><name sortKey="Charron, P" uniqKey="Charron P">P Charron</name></author><author><name sortKey="Dubourg, O" uniqKey="Dubourg O">O Dubourg</name></author><author><name sortKey="Kuhl, U" uniqKey="Kuhl U">U Kuhl</name></author><author><name sortKey="Maisch, B" uniqKey="Maisch B">B Maisch</name></author><author><name sortKey="Mckenna, Wj" uniqKey="Mckenna W">WJ McKenna</name></author><author><name sortKey="Monserrat, L" uniqKey="Monserrat L">L Monserrat</name></author><author><name sortKey="Pankuweit, S" uniqKey="Pankuweit S">S Pankuweit</name></author><author><name sortKey="Rapezzi, C" uniqKey="Rapezzi C">C Rapezzi</name></author><author><name sortKey="Seferovic, P" uniqKey="Seferovic P">P Seferovic</name></author><author><name sortKey="Tavazzi, L" uniqKey="Tavazzi L">L Tavazzi</name></author><author><name sortKey="Keren, A" uniqKey="Keren A">A Keren</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Flesch, M" uniqKey="Flesch M">M Flesch</name></author><author><name sortKey="Schwinger, Rh" uniqKey="Schwinger R">RH Schwinger</name></author><author><name sortKey="Schnabel, P" uniqKey="Schnabel P">P Schnabel</name></author><author><name sortKey="Schiffer, F" uniqKey="Schiffer F">F Schiffer</name></author><author><name sortKey="Gelder, I" uniqKey="Gelder I">I Gelder</name></author><author><name sortKey="Bavendiek, U" uniqKey="Bavendiek U">U Bavendiek</name></author><author><name sortKey="Sudkamp, M" uniqKey="Sudkamp M">M Südkamp</name></author><author><name sortKey="Kuhn Regnier, F" uniqKey="Kuhn Regnier F">F Kuhn-Regnier</name></author><author><name sortKey="Bohm, M" uniqKey="Bohm M">M Böhm</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hadcock, Jr" uniqKey="Hadcock J">JR Hadcock</name></author><author><name sortKey="Malbon, Cc" uniqKey="Malbon C">CC Malbon</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kentish, Jc" uniqKey="Kentish J">JC Kentish</name></author><author><name sortKey="Mccloskey, Dt" uniqKey="Mccloskey D">DT McCloskey</name></author><author><name sortKey="Layland, J" uniqKey="Layland J">J Layland</name></author><author><name sortKey="Palmer, S" uniqKey="Palmer S">S Palmer</name></author><author><name sortKey="Leiden, Jm" uniqKey="Leiden J">JM Leiden</name></author><author><name sortKey="Martin, Af" uniqKey="Martin A">AF Martin</name></author><author><name sortKey="Solaro, Rj" uniqKey="Solaro R">RJ Solaro</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kinoshota, E" uniqKey="Kinoshota E">E Kinoshota</name></author><author><name sortKey="Kinoshita Kikuta, E" uniqKey="Kinoshita Kikuta E">E Kinoshita-Kikuta</name></author><author><name sortKey="Takiyama, K" uniqKey="Takiyama K">K Takiyama</name></author><author><name sortKey="Koike, T" uniqKey="Koike T">T Koike</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kooij, V" uniqKey="Kooij V">V Kooij</name></author><author><name sortKey="Saes, M" uniqKey="Saes M">M Saes</name></author><author><name sortKey="Jaquet, K" uniqKey="Jaquet K">K Jaquet</name></author><author><name sortKey="Zaremba, R" uniqKey="Zaremba R">R Zaremba</name></author><author><name sortKey="Foster, Db" uniqKey="Foster D">DB Foster</name></author><author><name sortKey="Murphy, Am" uniqKey="Murphy A">AM Murphy</name></author><author><name sortKey="Remedios, C" uniqKey="Remedios C">C Remedios</name></author><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kranias, Eg" uniqKey="Kranias E">EG Kranias</name></author><author><name sortKey="Garvey, Jl" uniqKey="Garvey J">JL Garvey</name></author><author><name sortKey="Srivastava, Rd" uniqKey="Srivastava R">RD Srivastava</name></author><author><name sortKey="Solaro, Rj" uniqKey="Solaro R">RJ Solaro</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Leineweber, K" uniqKey="Leineweber K">K Leineweber</name></author><author><name sortKey="Rohe, P" uniqKey="Rohe P">P Rohe</name></author><author><name sortKey="Beilfuss, A" uniqKey="Beilfuss A">A Beilfuss</name></author><author><name sortKey="Wolf, C" uniqKey="Wolf C">C Wolf</name></author><author><name sortKey="Sporkmann, H" uniqKey="Sporkmann H">H Sporkmann</name></author><author><name sortKey="Bruck, H" uniqKey="Bruck H">H Bruck</name></author><author><name sortKey="Jakob, Hg" uniqKey="Jakob H">HG Jakob</name></author><author><name sortKey="Heusch, G" uniqKey="Heusch G">G Heusch</name></author><author><name sortKey="Philipp, T" uniqKey="Philipp T">T Philipp</name></author><author><name sortKey="Brodde, Oe" uniqKey="Brodde O">OE Brodde</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Makarenko, I" uniqKey="Makarenko I">I Makarenko</name></author><author><name sortKey="Opitz, Ca" uniqKey="Opitz C">CA Opitz</name></author><author><name sortKey="Leake, Mc" uniqKey="Leake M">MC Leake</name></author><author><name sortKey="Neagoe, C" uniqKey="Neagoe C">C Neagoe</name></author><author><name sortKey="Kulke, M" uniqKey="Kulke M">M Kulke</name></author><author><name sortKey="Gwathmey, Jk" uniqKey="Gwathmey J">JK Gwathmey</name></author><author><name sortKey="Monte, F" uniqKey="Monte F">F Monte</name></author><author><name sortKey="Hajjar, Rj" uniqKey="Hajjar R">RJ Hajjar</name></author><author><name sortKey="Linke, Wa" uniqKey="Linke W">WA Linke</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Messer, Ae" uniqKey="Messer A">AE Messer</name></author><author><name sortKey="Jacques, Am" uniqKey="Jacques A">AM Jacques</name></author><author><name sortKey="Marston, Sb" uniqKey="Marston S">SB Marston</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Messer, Ae" uniqKey="Messer A">AE Messer</name></author><author><name sortKey="Gallon, Ce" uniqKey="Gallon C">CE Gallon</name></author><author><name sortKey="Mckenna, Wj" uniqKey="Mckenna W">WJ McKenna</name></author><author><name sortKey="Remedios, Cg" uniqKey="Remedios C">CG Remedios</name></author><author><name sortKey="Marston, Sb" uniqKey="Marston S">SB Marston</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Muller, A" uniqKey="Muller A">A Muller</name></author><author><name sortKey="Linden, Gc" uniqKey="Linden G">GC Linden</name></author><author><name sortKey="Zuidwijk, Mj" uniqKey="Zuidwijk M">MJ Zuidwijk</name></author><author><name sortKey="Simonides, Ws" uniqKey="Simonides W">WS Simonides</name></author><author><name sortKey="Laarse, Wj" uniqKey="Laarse W">WJ Laarse</name></author><author><name sortKey="Hardeveld, C" uniqKey="Hardeveld C">C Hardeveld</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Nagueh, Sf" uniqKey="Nagueh S">SF Nagueh</name></author><author><name sortKey="Shah, G" uniqKey="Shah G">G Shah</name></author><author><name sortKey="Wu, Y" uniqKey="Wu Y">Y Wu</name></author><author><name sortKey="Torre Amione, G" uniqKey="Torre Amione G">G Torre-Amione</name></author><author><name sortKey="King, Nm" uniqKey="King N">NM King</name></author><author><name sortKey="Lahmers, S" uniqKey="Lahmers S">S Lahmers</name></author><author><name sortKey="Witt, Cc" uniqKey="Witt C">CC Witt</name></author><author><name sortKey="Becker, K" uniqKey="Becker K">K Becker</name></author><author><name sortKey="Labeit, S" uniqKey="Labeit S">S Labeit</name></author><author><name sortKey="Granzier, Hl" uniqKey="Granzier H">HL Granzier</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Neagoe, C" uniqKey="Neagoe C">C Neagoe</name></author><author><name sortKey="Kulke, M" uniqKey="Kulke M">M Kulke</name></author><author><name sortKey="Monte, F" uniqKey="Monte F">F Monte</name></author><author><name sortKey="Gwathmey, Jk" uniqKey="Gwathmey J">JK Gwathmey</name></author><author><name sortKey="Tombe, Pp" uniqKey="Tombe P">PP Tombe</name></author><author><name sortKey="Hajjar, Rj" uniqKey="Hajjar R">RJ Hajjar</name></author><author><name sortKey="Linke, Wa" uniqKey="Linke W">WA Linke</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Neumann, J" uniqKey="Neumann J">J Neumann</name></author><author><name sortKey="Gupta, Rc" uniqKey="Gupta R">RC Gupta</name></author><author><name sortKey="Schmitz, W" uniqKey="Schmitz W">W Schmitz</name></author><author><name sortKey="Scholz, H" uniqKey="Scholz H">H Scholz</name></author><author><name sortKey="Nairn, Ac" uniqKey="Nairn A">AC Nairn</name></author><author><name sortKey="Watanabe, Am" uniqKey="Watanabe A">AM Watanabe</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Neumann, J" uniqKey="Neumann J">J Neumann</name></author><author><name sortKey="Eschenhagen, T" uniqKey="Eschenhagen T">T Eschenhagen</name></author><author><name sortKey="Jones, Lr" uniqKey="Jones L">LR Jones</name></author><author><name sortKey="Linck, B" uniqKey="Linck B">B Linck</name></author><author><name sortKey="Schmitz, W" uniqKey="Schmitz W">W Schmitz</name></author><author><name sortKey="Scholz, H" uniqKey="Scholz H">H Scholz</name></author><author><name sortKey="Zimmermann, N" uniqKey="Zimmermann N">N Zimmermann</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Niclauss, N" uniqKey="Niclauss N">N Niclauss</name></author><author><name sortKey="Michel Reher, Mb" uniqKey="Michel Reher M">MB Michel-Reher</name></author><author><name sortKey="Alewijnse, Ae" uniqKey="Alewijnse A">AE Alewijnse</name></author><author><name sortKey="Michel, Mc" uniqKey="Michel M">MC Michel</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Packer, M" uniqKey="Packer M">M Packer</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Parodi, O" uniqKey="Parodi O">O Parodi</name></author><author><name sortKey="Maria, R" uniqKey="Maria R">R Maria</name></author><author><name sortKey="Oltrona, L" uniqKey="Oltrona L">L Oltrona</name></author><author><name sortKey="Testa, R" uniqKey="Testa R">R Testa</name></author><author><name sortKey="Sambuceti, G" uniqKey="Sambuceti G">G Sambuceti</name></author><author><name sortKey="Roghi, A" uniqKey="Roghi A">A Roghi</name></author><author><name sortKey="Merli, M" uniqKey="Merli M">M Merli</name></author><author><name sortKey="Belingheri, L" uniqKey="Belingheri L">L Belingheri</name></author><author><name sortKey="Accinni, R" uniqKey="Accinni R">R Accinni</name></author><author><name sortKey="Spinelli, F" uniqKey="Spinelli F">F Spinelli</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ungerer, M" uniqKey="Ungerer M">M Ungerer</name></author><author><name sortKey="Bohm, M" uniqKey="Bohm M">M Böhm</name></author><author><name sortKey="Elce, Js" uniqKey="Elce J">JS Elce</name></author><author><name sortKey="Erdmann, E" uniqKey="Erdmann E">E Erdmann</name></author><author><name sortKey="Lohse, Mj" uniqKey="Lohse M">MJ Lohse</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ungerer, M" uniqKey="Ungerer M">M Ungerer</name></author><author><name sortKey="Parruti, G" uniqKey="Parruti G">G Parruti</name></author><author><name sortKey="Bohm, M" uniqKey="Bohm M">M Böhm</name></author><author><name sortKey="Puzicha, M" uniqKey="Puzicha M">M Puzicha</name></author><author><name sortKey="Deblasi, A" uniqKey="Deblasi A">A DeBlasi</name></author><author><name sortKey="Erdmann, E" uniqKey="Erdmann E">E Erdmann</name></author><author><name sortKey="Lohse, Mj" uniqKey="Lohse M">MJ Lohse</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author><author><name sortKey="Papp, Z" uniqKey="Papp Z">Z Papp</name></author><author><name sortKey="Zaremba, R" uniqKey="Zaremba R">R Zaremba</name></author><author><name sortKey="Boontje, Nm" uniqKey="Boontje N">NM Boontje</name></author><author><name sortKey="Jong, Jw" uniqKey="Jong J">JW Jong</name></author><author><name sortKey="Owen, Vj" uniqKey="Owen V">VJ Owen</name></author><author><name sortKey="Burton, Pb" uniqKey="Burton P">PB Burton</name></author><author><name sortKey="Goldmann, P" uniqKey="Goldmann P">P Goldmann</name></author><author><name sortKey="Jaquet, K" uniqKey="Jaquet K">K Jaquet</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Heerebeek, L" uniqKey="Heerebeek L">L Heerebeek</name></author><author><name sortKey="Borbely, A" uniqKey="Borbely A">A Borbély</name></author><author><name sortKey="Niessen, Hw" uniqKey="Niessen H">HW Niessen</name></author><author><name sortKey="Bronzwaer, Jg" uniqKey="Bronzwaer J">JG Bronzwaer</name></author><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author><author><name sortKey="Linke, Wa" uniqKey="Linke W">WA Linke</name></author><author><name sortKey="Laarman, Gj" uniqKey="Laarman G">GJ Laarman</name></author><author><name sortKey="Paulus, Wj" uniqKey="Paulus W">WJ Paulus</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Vinge, Le" uniqKey="Vinge L">LE Vinge</name></author><author><name sortKey=" Ie, E" uniqKey=" Ie E">E Øie</name></author><author><name sortKey="Andersson, Y" uniqKey="Andersson Y">Y Andersson</name></author><author><name sortKey="Gr Gaard, Hk" uniqKey="Gr Gaard H">HK Grøgaard</name></author><author><name sortKey="Andersen, G" uniqKey="Andersen G">G Andersen</name></author><author><name sortKey="Attramadal, H" uniqKey="Attramadal H">H Attramadal</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wang, X" uniqKey="Wang X">X Wang</name></author><author><name sortKey="Dhalla, Ns" uniqKey="Dhalla N">NS Dhalla</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Weber, Kt" uniqKey="Weber K">KT Weber</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wolff, Mr" uniqKey="Wolff M">MR Wolff</name></author><author><name sortKey="Buck, Sh" uniqKey="Buck S">SH Buck</name></author><author><name sortKey="Stoker, Sw" uniqKey="Stoker S">SW Stoker</name></author><author><name sortKey="Greaser, Ml" uniqKey="Greaser M">ML Greaser</name></author><author><name sortKey="Mentzer, Rm" uniqKey="Mentzer R">RM Mentzer</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Zaremba, R" uniqKey="Zaremba R">R Zaremba</name></author><author><name sortKey="Merkus, D" uniqKey="Merkus D">D Merkus</name></author><author><name sortKey="Hamdani, N" uniqKey="Hamdani N">N Hamdani</name></author><author><name sortKey="Lamers, Jmj" uniqKey="Lamers J">JMJ Lamers</name></author><author><name sortKey="Paulus, Wj" uniqKey="Paulus W">WJ Paulus</name></author><author><name sortKey="Remedios, C" uniqKey="Remedios C">C Remedios</name></author><author><name sortKey="Duncker, Dj" uniqKey="Duncker D">DJ Duncker</name></author><author><name sortKey="Stienen, Gjm" uniqKey="Stienen G">GJM Stienen</name></author><author><name sortKey="Velden, J" uniqKey="Velden J">J Velden</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhang, R" uniqKey="Zhang R">R Zhang</name></author><author><name sortKey="Zhao, J" uniqKey="Zhao J">J Zhao</name></author><author><name sortKey="Mandveno, A" uniqKey="Mandveno A">A Mandveno</name></author><author><name sortKey="Potter, Jd" uniqKey="Potter J">JD Potter</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Muscle Res Cell Motil</journal-id><journal-title-group><journal-title>Journal of Muscle Research and Cell Motility</journal-title></journal-title-group><issn pub-type="ppub">0142-4319</issn><issn pub-type="epub">1573-2657</issn><publisher><publisher-name>Springer Netherlands</publisher-name><publisher-loc>Dordrecht</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">21132354</article-id><article-id pub-id-type="pmc">3005110</article-id><article-id pub-id-type="publisher-id">9231</article-id><article-id pub-id-type="doi">10.1007/s10974-010-9231-8</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Paper</subject></subj-group></article-categories><title-group><article-title>More severe cellular phenotype in human idiopathic dilated cardiomyopathy compared to ischemic heart disease</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Hamdani</surname><given-names>Nazha</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>Borbély</surname><given-names>Attila</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>Veenstra</surname><given-names>Sophie P. G. R.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>Kooij</surname><given-names>Viola</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>Vrydag</surname><given-names>Wim</given-names></name><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><name><surname>Zaremba</surname><given-names>Ruud</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>dos Remedios</surname><given-names>Cris</given-names></name><xref ref-type="aff" rid="Aff3">3</xref></contrib><contrib contrib-type="author"><name><surname>Niessen</surname><given-names>Hans W. M.</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Michel</surname><given-names>Martin C.</given-names></name><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><name><surname>Paulus</surname><given-names>Walter J.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>Stienen</surname><given-names>Ger J. M.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author" corresp="yes"><name><surname>van der Velden</surname><given-names>Jolanda</given-names></name><address><phone>31-20-4448124</phone><fax>31-20-4448255</fax><email>j.vandervelden@vumc.nl</email></address><xref ref-type="aff" rid="Aff1">1</xref></contrib><aff id="Aff1"><label>1</label>Laboratory for Physiology, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands</aff><aff id="Aff2"><label>2</label>Department of Pathology, Institute for Cardiovascular Research, VU University Medical Center Amsterdam, Amsterdam, The Netherlands</aff><aff id="Aff3"><label>3</label>Muscle Research Unit, Institute for Biomedical Research, The University of Sydney, Sydney, Australia</aff><aff id="Aff4"><label>4</label>Department of Pharmacology and Pharmacotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</aff></contrib-group><pub-date pub-type="epub"><day>4</day><month>12</month><year>2010</year></pub-date><pub-date pub-type="pmc-release"><day>4</day><month>12</month><year>2010</year></pub-date><pub-date pub-type="ppub"><month>12</month><year>2010</year></pub-date><volume>31</volume><issue>4</issue><fpage>289</fpage><lpage>301</lpage><history><date date-type="received"><day>9</day><month>8</month><year>2010</year></date><date date-type="accepted"><day>19</day><month>11</month><year>2010</year></date></history><permissions><copyright-statement>© The Author(s) 2010</copyright-statement></permissions><abstract><p>Activation of the β-adrenergic receptor (βAR) pathway is the main mechanism of the heart to increase cardiac output via protein kinase A (PKA)-mediated phosphorylation of cellular target proteins, and perturbations therein may contribute to cardiac dysfunction in heart failure. In the present study a comprehensive analysis was made of mediators of the βAR pathway, myofilament properties and cardiac structure in patients with idiopathic (IDCM; n = 13) and ischemic (ISHD; n = 10) cardiomyopathy in comparison to non-failing hearts (donor; n = 10) for the following parameters: βAR density, G-coupled receptor kinases 2 and 5, stimulatory and inhibitory G-proteins, phosphorylation of myofilament targets of PKA, protein phosphatase 1, phospholamban, SERCA2a and single myocyte contractility. All parameters exhibited the expected alterations of heart failure, but for most of them the extent of alteration was greater in IDCM than in ISHD. Histological analysis also revealed higher collagen in IDCM compared to ISHD. Alterations in the βAR pathway are more pronounced in IDCM than in ISHD and may reflect sequential changes in cellular protein composition and function. Our data indicate that cellular dysfunction is more severe in IDCM than in ISHD.</p></abstract><kwd-group><title>Keywords</title><kwd>β-Adrenergic receptor</kwd><kwd>Protein phosphorylation</kwd><kwd>Myofilament function</kwd><kwd>Cardiomyocyte</kwd><kwd>Collagen</kwd></kwd-group><custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© Springer Science+Business Media B.V. 2010</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="Sec1"><title>Introduction</title><p>During increased cardiac stress stimulation of the β-adrenergic receptors (βAR) exerts a positive inotropic and lusitropic effect on the heart, via activation of protein kinase A (PKA)-mediated phosphorylation of Ca<sup>2+</sup>-handling and contractile proteins (Bers <xref ref-type="bibr" rid="CR3">2002</xref>; Brodde and Michel. <xref ref-type="bibr" rid="CR7">1999</xref>; Kranias et al. <xref ref-type="bibr" rid="CR20">1985</xref>; Kentish et al. <xref ref-type="bibr" rid="CR17">2001</xref>; Zhang et al. <xref ref-type="bibr" rid="CR43">1995</xref>). The positive inotropic effect largely originates from increased cytosolic [Ca<sup>2+</sup>] during the systolic phase of the cardiac cycle. The positive lusitropic effect results from increased cytosolic Ca<sup>2+</sup> re-uptake into the sarcoplasmic reticulum, increased Ca<sup>2+</sup> removal out of the cardiomyocyte, and desensitization of the myofilaments for Ca<sup>2+</sup>. In patients with heart failure (HF) the sympathetic nervous system is chronically activated to maintain perfusion of vital organs via peripheral vasoconstriction and via an increase in heart rate and in myocardial contractility. Although aimed at maintaining cardiac pump function, chronic neurohumoral stimulation is detrimental for cardiac function and results in uncoupling and down-regulation of mediators of the βAR pathway (Brodde and Michel <xref ref-type="bibr" rid="CR7">1999</xref>; Packer <xref ref-type="bibr" rid="CR31">1995</xref>). Abnormalities in this pathway have been implicated as important determinants of diminished function of the failing human heart. The adverse effects of neurohumoral overstimulation is illustrated by the negative correlation between noradrenaline plasma levels and prognosis of the patients (Cohn et al. <xref ref-type="bibr" rid="CR11">1984</xref>), and by the improvement of symptoms and prolonged survival of patients treated with β-blockers (Bohm and Maack <xref ref-type="bibr" rid="CR4">2000</xref>). In line with reduced β-adrenergic signaling, previous studies in end-stage HF patients with idiopathic cardiomyopathy showed reduced PKA-mediated phosphorylation of downstream myofilament target proteins, cardiac myosin binding protein C (cMyBP-C) and troponin I (cTnI) (El-Armouche et al. <xref ref-type="bibr" rid="CR13">2007</xref>; van der Velden et al. <xref ref-type="bibr" rid="CR35">2003</xref>; Messer et al. <xref ref-type="bibr" rid="CR23">2007</xref>, <xref ref-type="bibr" rid="CR24">2009</xref>; Copeland et al. <xref ref-type="bibr" rid="CR12">2010</xref>), which coincided with increased myofilament Ca<sup>2+</sup>-sensitivity (pCa<sub>50</sub>). In patients with diastolic heart failure (i.e., HF with preserved ejection fraction, HFPEF) hypophosphorylation of titin has been associated with increased cardiomyocyte stiffness (F<sub>passive</sub>) (Borbély et al. <xref ref-type="bibr" rid="CR6">2009</xref>). Insight in the modifications of the β-adrenergic pathway and coincident changes in cardiomyocyte function is needed to develop targeted therapy in HF patients. In a recent study we reported diverse changes at the myocardial ultrastructural level with prominent cardiomyocyte hypertrophy in HFPEF patients and low myofibrillar density in HF patients with reduced EF (HFREF) (van Heerebeek et al. <xref ref-type="bibr" rid="CR36">2006</xref>). Moreover, F<sub>passive</sub> was higher in HFPEF than in HFREF. These cellular differences may alter responsiveness to current HF treatment, which includes β-blocker therapy. Likewise, patients with idiopathic (IDCM) and ischemic (ISHD) cardiomyopathy may show diverse cellular changes.</p><p>Although many studies investigated mediators of the βAR signaling pathway and sarcomeric function in human heart failure, a direct comparative investigation of both in samples from IDCM and ISHD patients is lacking. Within the present study a systematic analysis was performed from the βAR to sarcomeric protein composition and function in IDCM and ISHD patients, and compared to non-failing donor myocardium (donor). Radioligand binding studies were performed to determine βAR density. Protein analysis included down-stream components of the adrenergic signalling cascade, the phospho-proteome of the myofilaments, and SERCA2a and phospholamban levels. Myofilament function was determined in permeabilized single cardiomyocytes. Histological analysis included cardiomyocyte diameter, collagen volume fraction and myofibrillar density.</p></sec><sec id="Sec2" sec-type="methods"><title>Methods</title><sec id="Sec3"><title>Human ventricular tissue</title><p>Left ventricular (LV) tissue samples were obtained during heart transplantation surgery from end-stage HF patients (NYHA III-IV) with IDCM (n = 13; 10 males, 3 females; mean age 51 ± 2 years) or ISHD (n = 10; 7 males, 3 females; mean age 51 ± 2 years)(Table <xref rid="Tab1" ref-type="table">1</xref>). Patients were classified to idiopathic dilated cardiomyopathy when the heart showed LV dilatation and LV systolic dysfunction with no identifiable cause and in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed myocardial abnormality (Elliott et al. <xref ref-type="bibr" rid="CR14">2008</xref>). In contrast, patients with ischemic heart disease had a history of myocardial infarction and explanted hearts showed severe coronary artery disease upon pathologic inspection. Medication included angiotension-converting-enzyme inhibitors, angiotensin II receptor antagonists, diuretics, β-blockers, digoxin and anti-arrhythmic agents and did not differ between the IDCM and ISHD group. Tissue from 10 donor hearts (Table <xref rid="Tab1" ref-type="table">1</xref>; 8 males, 2 females; mean age 38 ± 6 years) served as reference for non-failing myocardium. The tissue was collected in cardioplegic solution and stored in liquid nitrogen. Samples were obtained after informed consent and with approval of the local Ethical Committee (St Vincents’ Hospital Human Research Ethics Committee, Sydney, Australia: File number: H03/118; Title: Molecular Analysis of Human Heart Failure). The investigation conforms with the principles outlined in the Declaration of Helsinki (<xref ref-type="bibr" rid="CR41">1997</xref>).<table-wrap id="Tab1"><label>Table 1</label><caption><p>Patient/heart characteristics</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left"></th><th align="left">Sex</th><th align="left">Age</th><th align="left">cMyBP-C-P ProQ</th><th align="left">cTnI-P ProQ</th><th align="left">cTnI-P Phos-tag</th><th align="left">pCa<sub>50</sub></th></tr></thead><tbody><tr><td align="left">ISHD1</td><td align="left">Male</td><td char="." align="char">47</td><td char="." align="char">0.27</td><td char="." align="char">0.20</td><td align="left">0.14</td><td align="left">5.69</td></tr><tr><td align="left">ISHD2</td><td align="left">Male</td><td char="." align="char">50</td><td char="." align="char">0.36</td><td char="." align="char">0.41</td><td align="left">0.54</td><td align="left">5.60</td></tr><tr><td align="left">ISHD3</td><td align="left">Female</td><td char="." align="char">43</td><td char="." align="char">0.42</td><td char="." align="char">0.50</td><td align="left">–</td><td align="left">–</td></tr><tr><td align="left">ISHD4</td><td align="left">Male</td><td char="." align="char">45</td><td char="." align="char">0.21</td><td char="." align="char">0.32</td><td align="left">–</td><td align="left">–</td></tr><tr><td align="left">ISHD5</td><td align="left">Female</td><td char="." align="char">54</td><td char="." align="char">0.46</td><td char="." align="char">0.67</td><td align="left">0.79</td><td align="left">5.41</td></tr><tr><td align="left">ISHD6</td><td align="left">Male</td><td char="." align="char">55</td><td char="." align="char">0.67</td><td char="." align="char">2.20</td><td align="left">–</td><td align="left">5.70</td></tr><tr><td align="left">ISHD7</td><td align="left">Male</td><td char="." align="char">54</td><td char="." align="char">0.40</td><td char="." align="char">1.25</td><td align="left">1.70</td><td align="left">5.50</td></tr><tr><td align="left">ISHD8</td><td align="left">Male</td><td char="." align="char">54</td><td char="." align="char">0.31</td><td char="." align="char">0.33</td><td align="left">0.44</td><td align="left">5.73</td></tr><tr><td align="left">ISHD9</td><td align="left">Male</td><td char="." align="char">50</td><td char="." align="char">0.33</td><td char="." align="char">0.21</td><td align="left">1.18</td><td align="left">5.45</td></tr><tr><td align="left">ISHD10</td><td align="left">Male</td><td char="." align="char">61</td><td char="." align="char">0.20</td><td char="." align="char">0.13</td><td align="left">0.74</td><td align="left">5.56</td></tr><tr><td align="left">IDCM1</td><td align="left">Male</td><td char="." align="char">56</td><td char="." align="char">0.30</td><td char="." align="char">0.07</td><td align="left">0</td><td align="left">5.65</td></tr><tr><td align="left">IDCM2</td><td align="left">Male</td><td char="." align="char">27</td><td char="." align="char">0.32</td><td char="." align="char">0.11</td><td align="left">0</td><td align="left">5.65</td></tr><tr><td align="left">IDCM3</td><td align="left">Male</td><td char="." align="char">53</td><td char="." align="char">0.31</td><td char="." align="char">0</td><td align="left">–</td><td align="left">5.65</td></tr><tr><td align="left">IDCM4</td><td align="left">Male</td><td char="." align="char">53</td><td char="." align="char">0.44</td><td char="." align="char">0.22</td><td align="left">0.38</td><td align="left">5.59</td></tr><tr><td align="left">IDCM5</td><td align="left">Male</td><td char="." align="char">53</td><td char="." align="char">0.29</td><td char="." align="char">0.64</td><td align="left">–</td><td align="left">–</td></tr><tr><td align="left">IDCM6</td><td align="left">Male</td><td char="." align="char">62</td><td char="." align="char">0.25</td><td char="." align="char">0.16</td><td align="left">0.47</td><td align="left">–</td></tr><tr><td align="left">IDCM7</td><td align="left">Male</td><td char="." align="char">53</td><td char="." align="char">0.18</td><td char="." align="char">0.38</td><td align="left">0.46</td><td align="left">–</td></tr><tr><td align="left">IDCM8</td><td align="left">Male</td><td char="." align="char">44</td><td char="." align="char">0.50</td><td char="." align="char">0.33</td><td align="left">1.18</td><td align="left">–</td></tr><tr><td align="left">IDCM9</td><td align="left">Female</td><td char="." align="char">50</td><td char="." align="char">0.28</td><td char="." align="char">0.16</td><td align="left">0.65</td><td align="left">5.65</td></tr><tr><td align="left">IDCM10</td><td align="left">Male</td><td char="." align="char">53</td><td char="." align="char">0.25</td><td char="." align="char">0.08</td><td align="left">0.46</td><td align="left">5.52</td></tr><tr><td align="left">IDCM11</td><td align="left">Female</td><td char="." align="char">52</td><td char="." align="char">0.18</td><td char="." align="char">0.17</td><td align="left">0.51</td><td align="left">5.68</td></tr><tr><td align="left">IDCM12</td><td align="left">Male</td><td char="." align="char">58</td><td char="." align="char">0.19</td><td char="." align="char">0.12</td><td align="left">0.49</td><td align="left">5.71</td></tr><tr><td align="left">IDCM13</td><td align="left">Female</td><td char="." align="char">45</td><td char="." align="char">0.32</td><td char="." align="char">0.10</td><td align="left">–</td><td align="left">–</td></tr><tr><td align="left">DONOR1</td><td align="left">Male</td><td char="." align="char">39</td><td char="." align="char">0.62</td><td char="." align="char">1.96</td><td align="left">1.75</td><td align="left">5.65</td></tr><tr><td align="left">DONOR2</td><td align="left">Male</td><td char="." align="char">56</td><td char="." align="char">0.69</td><td char="." align="char">2.09</td><td align="left">1.94</td><td align="left">5.48</td></tr><tr><td align="left">DONOR3</td><td align="left">Male</td><td char="." align="char">21</td><td char="." align="char">0.60</td><td char="." align="char">4.54</td><td align="left">1.59</td><td align="left">5.48</td></tr><tr><td align="left">DONOR4</td><td align="left">Female</td><td char="." align="char">37</td><td char="." align="char">0.61</td><td char="." align="char">1.11</td><td align="left">1.57</td><td align="left">5.44</td></tr><tr><td align="left">DONOR5</td><td align="left">Male</td><td char="." align="char">23</td><td char="." align="char">0.64</td><td char="." align="char">0.94</td><td align="left">1.74</td><td align="left">5.52</td></tr><tr><td align="left">DONOR6</td><td align="left">Male</td><td char="." align="char">19</td><td char="." align="char">0.75</td><td char="." align="char">1.96</td><td align="left">1.97</td><td align="left">5.51</td></tr><tr><td align="left">DONOR7</td><td align="left">Female</td><td char="." align="char">53</td><td char="." align="char">0.73</td><td char="." align="char">1.12</td><td align="left">1.92</td><td align="left">–</td></tr><tr><td align="left">DONOR8</td><td align="left">Male</td><td char="." align="char">13</td><td char="." align="char">0.75</td><td char="." align="char">1.75</td><td align="left">–</td><td align="left">5.43</td></tr><tr><td align="left">DONOR9</td><td align="left">Male</td><td char="." align="char">65</td><td char="." align="char">0.49</td><td char="." align="char">1.09</td><td align="left">0.98</td><td align="left">5.63</td></tr><tr><td align="left">DONOR10</td><td align="left">Male</td><td char="." align="char">51</td><td char="." align="char">0.57</td><td char="." align="char">1.56</td><td align="left">–</td><td align="left">–</td></tr></tbody></table><table-wrap-foot><p>Age and sex of all patients and donors with the corresponding mean value for cMyBP-C and cTnI phosphorylation determined on ProQ Diamond stained gels (values in arbitrary units), for cTnI phosphorylation assessed by Phos-tag (in mol per mol cTnI) and for Ca<sup>2+</sup>-sensitivity of force</p></table-wrap-foot></table-wrap></p></sec><sec id="Sec4"><title>Protein analysis</title><sec id="Sec5"><title>Radioligand binding</title><p>Tissue samples (<bold>~</bold>200 mg wet weight) were thawed in ice-cold 1 mM KHCO<sub>3</sub> solution, minced with scissors and then homogenized with an Ultra-Turrax (Janke & Kunkel, Staufen, Germany) for 10 s at maximum speed followed by twice 20 s at 2/3 of maximum speed. The homogenates were centrifuged for 15 min at 250×<italic>g</italic> and 4°C. The supernatant was filtered through medical gauze and centrifuged for 20 min at 50,000×<italic>g</italic> at 4°C. The sediment was resuspended in binding buffer (10 mM Tris, 154 mM NaCl, pH 7.4). Protein content was measured by the method of Bradford using bovine IgG as standard. Radioligand binding was performed as described earlier (Niclauss et al. <xref ref-type="bibr" rid="CR30">2006</xref>) using a 90 min incubation at 37°C with [<sup>125</sup>I]iodocyanopindolol (ICYP; specific activity 2200 Ci/mmol, Perkin Elmer, Zaventem, Belgium) in a total volume of 250 μl. Non-specific binding was defined as binding in the presence of 100 μM isoproterenol (Sigma-Aldrich). All experiments were performed in duplicates in 96 well plates, and incubations were terminated by rapid vacuum filtration over Whatman GF/C using a Filtermate harvester (Perkin Elmer). Each filter was washed with approximately 10 ml of buffer. Radioactivity adherent to the filters was quantified in a Topcount NXT (Perkin Elmer) using Microsint O scintillator (Perkin Elmer). To determine the relative amount of β<sub>1</sub>AR and β<sub>2</sub>AR, membranes were incubated with ICYP (100 pM) in the presence or absence of eight concentrations (range 10<sup>−10</sup> to 10<sup>−3</sup> M) of the highly selective β<sub>1</sub>AR antagonist CGP 20712A (1-[2-((3-carbamoyl-4-hydroxy) phenoxy)ethylamino]-3-[4-(1-methyl-4-trifluoromethyl-2-imidazolyl)phenoxy]-2-propanol methanesulfonate).</p></sec><sec id="Sec6"><title>Components of the β-adrenergic receptor pathway</title><p>Protein expression levels of G-coupled receptor kinases (GRK2 and GRK5), G-proteins (G<sub>s</sub> and G<sub>i</sub>) and protein phosphatase 1 (PP-1) were analyzed by one-dimensional 15% SDS-polyacrylamide gel electrophoresis (1D-PAGE) and subsequent Western blotting. Samples were applied in concentrations which were within the linear range of detection: 20 μg for GRK2, GRK5, G<sub>s</sub> and PP-1, and 10 μg for G<sub>i</sub>. Blots were pre-incubated with 0.5% milk powder in TTBS (Tween-tris-buffered-saline: 10 mM Tris–HCl pH 7.6, 75 mM NaCl, 0.1% Tween) for 1 h at room temperature. The blots were incubated overnight at 4°C with primary rabbit polyclonal antibodies (Santa Cruz) against GRK2 (dilution 1:1000; sc-562), GRK5 (dilution 1:1000; sc-565), G<sub>s</sub> (G<sub>s/olf</sub>; dilution 1:1000; sc-383), G<sub>i</sub> (dilution 1:1000; G<sub>i-1</sub> sc-262, G<sub>i-2</sub> sc-7276, G<sub>i-3</sub> sc-262) or primary mouse polyclonal antibody against PP-1 (dilution 1:50; sc-7482, Santa Cruz). Specificity of the antibodies has been shown in previous studies (Vinge et al. <xref ref-type="bibr" rid="CR37">2001</xref>; Cho and Kehrl <xref ref-type="bibr" rid="CR10">2007</xref>) and all antibodies revealed one protein band in our Western blot analysis indicative for their specificity. Primary antibody binding was visualized using a secondary horseradish peroxidase-labeled goat-anti-rabbit/mouse antibody (dilution 1:2000; DakoCytomation) and enhanced chemiluminescence (ECL plus Western blotting detection, Amersham Biosciences). All signals were normalized to actin (dilution 1:1000; clone KJ43A; Sigma) stained on the same blots.</p></sec><sec id="Sec7"><title>Myofilament protein phosphorylation</title><p>Myofilament protein phosphorylation was determined using Pro-Q Diamond Phosphoprotein Stain as described previously (Zaremba et al. <xref ref-type="bibr" rid="CR42">2007</xref>). To preserve the endogenous phosphorylation status, frozen biopsies were homogenized in liquid nitrogen and re-suspended in 1 ml cold 10% trichloroacetic acid solution (TCA; dissolved in acetone containing 0.1% (w/v) dithiothreitol (DTT)). TCA-treated tissue pellets were homogenized in sample buffer containing 15% glycerol, 62.5 mM Tris (pH 6.8), 1% (w/v) SDS and 2% (w/v) DTT. Tissue samples were separated on gradient gels (Criterion tris–HCl 4–15% gel, BioRad) and proteins were stained for one hour with Pro-Q Diamond Phosphoprotein Stain. Fixation, washing and de-staining were performed according to the manufacturer’s guidelines (Molecular Probes). To assess protein content subsequently gels were stained overnight with SYPRO Ruby stain (Molecular Probes). Phosphorylation status of myofilament proteins was expressed relative to protein expression of cMyBP-C to correct for differences in sample loading. Staining was visualized using the LAS-3000 Image Reader and signals were analyzed with AIDA.</p><p>Cardiac troponin I phosphorylation at PKA sites Ser 23/24 was detected with a primary rabbit polyclonal antibody (dilution 1:500; Cell signaling) in Western blotting. In addition, the recently developed Phos-tag<sup>TM</sup> acrylamide (FMS Laboratory; Hiroshima University, Japan) (Kinoshota et al. <xref ref-type="bibr" rid="CR18">2006</xref>) was used to visualize phosphorylated cTnI species using alkoxide-bridged dinuclear metal (Mn<sup>2+</sup>) complex as phosphate-binding tag (Phos-tag) molecule. Mn<sup>2+</sup>-Phos-tag molecules preferentially capture phosphomonoester dianions bound to Ser, Thr and Tyr residues. Non-phosphorylated and phosphorylated cTnI species were separated in 1D-PAGE with polyacrylamide-bound Mn<sup>2+</sup>-Phos-tag and transferred to Western blots. Phosphorylated cTnI species in the gel are visualized as slower migration bands compared to the corresponding dephosphorylated cTnI form (Kooij et al. <xref ref-type="bibr" rid="CR19">2010</xref>; Messer et al. <xref ref-type="bibr" rid="CR24">2009</xref>).</p></sec><sec id="Sec8"><title>SERCA2a and phospholamban</title><p>SERCA2a protein levels were determined immunochemically by dot-blot analysis, as described before, with minor modifications (Muller et al. <xref ref-type="bibr" rid="CR25">1991</xref>). Briefly, homogenized tissue samples (typically 0.5 μg total protein) were spotted in triplo onto a nitrocellulose membrane. The blot was then incubated with a 1:2500 dilution of a polyclonal antiserum to SERCA2a and subsequently with 125I-labeled anti-rabbit immunoglobulin G (0.05 mg/ml, specific activity 7 mCi/mg). To detect phospholamban, blots were first incubated with a 1:2500 dilution of a monoclonal anti mouse antibody (Affinity Bioreagents) and subsequently with 125I-labeled anti-mouse immunoglobulin G. Blots were exposed to Phosphor Imager screens, which were then scanned and spots were quantified using ImageQuant software (Molecular Dynamics). All protein values for ISHD and IDCM samples were normalized to the average value observed in donor, which was set to 1.</p></sec></sec><sec id="Sec9"><title>Force measurements in single cardiomyocytes</title><p>Force measurements were performed in single, mechanically isolated cardiomyocytes as described previously (Kooij et al. <xref ref-type="bibr" rid="CR19">2010</xref>; van der Velden et al. <xref ref-type="bibr" rid="CR35">2003</xref>). Tissue samples were defrosted in relaxing solution (in mmol/l: free Mg, 1; KCl, 145; EGTA, 2; MgATP, 4; imidazole, 10; pH 7.0), mechanically disrupted and incubated for 5 min in relaxing solution supplemented with 0.5% Triton X-100 to remove all membrane structures. Subsequently, cells were washed twice in relaxing solution, after which single cardiomyocytes were attached with silicone adhesive between a force transducer and a motor. Sarcomere length of isolated cardiomyocytes was adjusted to 2.2 μm. The pCa (−<sub>10</sub>log[Ca<sup>2+</sup>]) ranged from 9.0 (relaxation solution) to 4.5 (maximal activation). All force values were normalized for cardiomyocyte cross-sectional area. Exposure to a series of solutions with intermediate pCa values (pCa 6.0–5.0) yielded the baseline force-pCa relation. On transfer of the cardiomyocyte from relaxing to activating solution, isometric force started to develop. Once a steady state force level was reached, the cell was shortened within 1 ms to 80% of its original length to determine the baseline of the force transducer. The distance between the baseline and the steady force level is the total force (F<sub>total</sub>). After 20 ms, the cell was restretched and returned to the relaxing solution, in which a second slack test, of 10 s duration was performed to determine passive force (F<sub>passive</sub>). Active force was obtained by subtracting passive force from the total force, i.e., F<sub>active</sub> = F<sub>total</sub> − F<sub>passive</sub>.</p></sec><sec id="Sec10"><title>Quantitative histomorphometry</title><p>Histomorphologic analysis of tissues was performed on elastica-von-Giesson and hematoxylin-eosin-stained 4 μm thick sections of tissue fixed in 5% formalin (Borbély et al. <xref ref-type="bibr" rid="CR5">2005</xref>). Images of these sections were acquired using a projection microscope (×50). Subsequent image analysis, using SlidebookTM 4.0 software (3I, Denver, Co), was performed to determine cardiomyocyte diameter and the extent of interstitial fibrosis, which was expressed as collagen volume fraction. Areas of reparative and perivascular fibrosis were excluded. Cardiomyocyte diameter was determined perpendicularly to the outer contour of the cell membrane at nucleus level in 15 representative myocytes of the cardiac tissue section, and collagen volume fraction was calculated as the sum of all connective tissue areas divided by the sum of all connective tissue and muscle areas averaged over 4–6 representative fields of the cardiac tissue section. Data were averaged per heart sample and averaged to obtain the mean of the group. For analysis of cardiomyocyte diameter and collagen volume fraction 9 ISHD, 7 IDCM and 5 donor hearts were included.</p><p>Analysis of myofibrillar density was performed in 8 ISHD, 6 IDCM and 5 donor hearts. Tissues samples were fixed in 2% (v/v) gluteraldehyde for 30 min and 1.5% (w/v) osmium tetroxide for 10 min dehydrated with acetone and embedded in Epon812. Ultrathin sections were collected on 300-mesh Formavar-coated Nickel-grids. The sections were contrasted with uranyl acetate and lead citrate and were examined in a Jeol-1200EX electron microscope. Quantitative analysis was performed with the above mentioned automated image analyzer. Cardiomyocyte myofibrillar density was calculated from the sum of the myofibrillar areas related to total cellular area in 4–6 representative myocytes per sample. Data were averaged per heart.</p></sec><sec id="Sec11"><title>Data analysis</title><p>Competition binding data were analyzed by fitting mono- and biphasic sigmoidal functions to the experimental data; a biphasic fit was accepted only if it resulted in a significant improvement as judged by an F-test. Resulting IC<sub>50</sub> values for the high and low affinity component of inhibition were converted to K<sub>i</sub> values based upon the Cheng–Prusoff equation (Cheng and Prusoff <xref ref-type="bibr" rid="CR9">1973</xref>) and assuming a K<sub>d</sub> value of ICYP of 72 pM (n = 4). Due to limited tissue availability, receptor density (B<sub>max</sub>) was estimated based upon the specific binding (SB) of the single radioligand concentration (L) in the competition experiments relative to its K<sub>d</sub> using the equation B<sub>max</sub> = SB/(1 − 1/(L/K<sub>d</sub> + 1)). The statistical significance of inter-group differences was assessed by one-way ANOVA followed by Dunnett’s post-hoc tests.</p><p>Values are given as mean ± SEM of n observations. The mean data values of protein and histological analysis and force measurements in ISHD, IDCM and donor samples were compared using one-way ANOVA and Bonferroni-post tests. <italic>P</italic> < 0.05 was considered significant. All statistical analysis was performed with Prism (version 4.01, Graphpad Software, San Diego, CA, USA).</p></sec></sec><sec id="Sec12"><title>Results</title><sec id="Sec13"><title>Components of the β-adrenergic receptor pathway</title><p>In all cases except one competition by the highly β<sub>1</sub>-selective antagonist CGP 20712A resulted in biphasic curves (Fig. <xref rid="Fig1" ref-type="fig">1</xref>a). The −log K<sub>i</sub> values for high and low affinity sites, which identify β<sub>1</sub>AR and β<sub>2</sub>AR, respectively, were not significantly different between IDCM (8 hearts; 8.21 ± 0.19 and 5.59 ± 0.09) and ISHD (8 hearts; 8.17 ± 0.09 and 5.62 ± 0.10) myocardium, and did not differ from the values observed in donor (7 hearts; 8.55 ± 0.12 and 5.74 ± 0.11). Single point estimates of total βAR density, revealed significantly reduced βAR density in IDCM compared to donor, while the value observed in ISHD was intermediate between IDCM and donor (Fig. <xref rid="Fig1" ref-type="fig">1</xref>b). The percentage of β<sub>1</sub>ARs did not differ between IDCM (50 ± 4%) and ISHD (47 ± 9%) samples and was comparable to the value observed in donor (52 ± 6%).<fig id="Fig1"><label>Fig. 1</label><caption><p><bold>a</bold> Competition curve of radioligand binding as a function of CGP 20712A. <bold>b</bold> βAR density was significantly lower in IDCM compared to donor, but the receptor distribution was the same. <bold>c</bold> Western blot examples of βAR pathway proteins in IDCM, ISHD and donor. Expression of Gs was significantly lower in failing compared to donor, but did not differ between IDCM and ISHD. <bold>d</bold> The expression level of G<sub>iα-1</sub> was significantly increased in IDCM compared to donor, while ISHD did not differ from donor. *<italic>P</italic> < 0.05 in Bonferroni-post tests, IDCM versus ISHD; <sup>#</sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor. Donor values obtained in Western blot analyses were set to 1</p></caption><graphic xlink:href="10974_2010_9231_Fig1_HTML" id="MO1"></graphic></fig></p><p>No difference was found in expression of GRK2 between IDCM and ISHD, while GRK5 was significantly higher in ISHD than in IDCM myocardium (Table <xref rid="Tab2" ref-type="table">2</xref>). Compared to donor GRK2 was significantly lower in both failing groups, while GRK5 was significantly higher in the ISHD group. G<sub>s</sub> expression did not differ between ISHD and IDCM, though was significantly lower in both failing groups compared to donor (Fig. <xref rid="Fig1" ref-type="fig">1</xref>c; Table <xref rid="Tab2" ref-type="table">2</xref>). In addition to G<sub>s</sub>, we have analyzed three isoforms of inhibitory G-protein: G<sub>iα-1</sub>, G<sub>iα-2</sub> and G<sub>iα-3</sub>. The heterotrimeric G-proteins are composed of α, β and γ subunits, of which the α-subunit confers specificity to the G-protein (Wang and Dhalla <xref ref-type="bibr" rid="CR38">2000</xref>). G<sub>iα-1</sub> expression was significantly higher in IDCM than in ISHD and donor (Fig. <xref rid="Fig1" ref-type="fig">1</xref>d), while G<sub>iα-2</sub> was significantly higher in both failing groups compared to donor (Table <xref rid="Tab2" ref-type="table">2</xref>).The G<sub>iα-3</sub> expression level was not altered in patient groups (data are summarized in Table <xref rid="Tab2" ref-type="table">2</xref>).<table-wrap id="Tab2"><label>Table 2</label><caption><p>Protein analysis</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left"></th><th align="left">ISHD (n = 9)</th><th align="left">IDCM (n = 13)</th><th align="left">Donor (n = 8)</th></tr></thead><tbody><tr><td align="left">GRK2 (a.u.)</td><td char="±" align="char">0.72 ± 0.07<sup>#</sup></td><td char="±" align="char">0.62 ± 0.13<sup>#</sup></td><td char="±" align="char">1.00 ± 0.07</td></tr><tr><td align="left">GRK5 (a.u.)</td><td char="±" align="char">1.92 ± 0.23<sup>#</sup></td><td char="±" align="char">1.33 ± 0.19*</td><td char="±" align="char">1.00 ± 0.20</td></tr><tr><td align="left">Gs (a.u.)</td><td char="±" align="char">0.39 ± 0.10<sup>#</sup></td><td char="±" align="char">0.45 ± 0.13<sup>#</sup></td><td char="±" align="char">1.00 ± 0.30</td></tr><tr><td align="left">Giα-1 (a.u.)</td><td char="±" align="char">1.00 ± 0.20</td><td char="±" align="char">3.36 ± 0.91<sup>#,</sup>*</td><td char="±" align="char">1.00 ± 0.30</td></tr><tr><td align="left">Giα-2 (a.u.)</td><td char="±" align="char">2.17 ± 0.40<sup>#</sup></td><td char="±" align="char">3.18 ± 0.80<sup>#</sup></td><td char="±" align="char">1.00 ± 0.10</td></tr><tr><td align="left">Giα-3 (a.u.)</td><td char="±" align="char">0.81 ± 0.18</td><td char="±" align="char">1.19 ± 0.30</td><td char="±" align="char">1.00 ± 0.30</td></tr><tr><td align="left">MLC-2P (a.u.)</td><td char="±" align="char">1.60 ± 0.22<sup>#</sup></td><td char="±" align="char">0.89 ± 0.16*</td><td char="±" align="char">1.00 ± 0.07</td></tr><tr><td align="left">PP-1 (a.u.)</td><td char="±" align="char">1.51 ± 0.19</td><td char="±" align="char">2.45 ± 0.35<sup>#,</sup>*</td><td char="±" align="char">1.00 ± 0.40</td></tr><tr><td align="left">Phospholamban (a.u.)</td><td char="±" align="char">1.43 ± 0.14<sup>#</sup></td><td char="±" align="char">1.55 ± 0.08<sup>#</sup></td><td char="±" align="char">1.00 ± 0.04</td></tr><tr><td align="left">SERCA2a (a.u.)</td><td char="±" align="char">0.99 ± 0.07</td><td char="±" align="char">0.72 ± 0.06<sup>#,</sup>*</td><td char="±" align="char">1.00 ± 0.07</td></tr></tbody></table><table-wrap-foot><p>All signals in IDCM and ISHD samples were normalized to the averaged value observed in donor, which was set to 1. <italic>GRK</italic> G-coupled receptor kinase, <italic>Gs</italic> G-stimulatory, <italic>Gi</italic> G-inhibitory, <italic>MLC-2P</italic> phosphorylated myosin light chain 2, <italic>PP-1</italic> protein phosphatase 1. <italic>a.u.</italic> arbitrary units, <italic>n</italic> number of heart samples. * <italic>P</italic> < 0.05 in Bonferroni-post tests, IDCM versus ISHD; <sup># </sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor</p></table-wrap-foot></table-wrap></p></sec><sec id="Sec14"><title>Myofilament and calcium handling proteins</title><p>ProQ Diamond phosphostaining was used to detect phosphorylation of myofilament proteins. Figure <xref rid="Fig2" ref-type="fig">2</xref>a shows ProQ Diamond-stained cardiac samples from ISHD, donor (D) and IDCM myocardium separated on a gradient gel. The same gel was subsequently stained with SYPRO Ruby for analysis of total protein content (Fig. <xref rid="Fig2" ref-type="fig">2</xref>b). The ProQ Diamond stained gel shows lower endogenous phosphorylation of the PKA-target proteins cMyBP-C and cTnI in failing compared to -donor. Noteworthy, cTnI phosphorylation was significantly higher in ISHD compared to IDCM (Fig. <xref rid="Fig2" ref-type="fig">2</xref>c). In addition, phosphorylation of cMyBP-C was higher in ISHD compared to IDCM, though not significantly (<italic>P</italic> = 0.07). When the failing and donor were combined, a monovariate linear regression analysis revealed significant correlations between the ProQ Diamond-assessed phosphorylation status of cMyBPC and cTnI (<italic>P</italic> < 0.0001; R<sup>2</sup> = 0.75) (Fig. <xref rid="Fig2" ref-type="fig">2</xref>d).<fig id="Fig2"><label>Fig. 2</label><caption><p><bold>a</bold> ProQ Diamond-stained and <bold>b</bold> SYPRO-stained gel of ISHD, donor (<italic>D</italic>) and IDCM samples. The ProQ Diamond stained gel clearly shows higher phosphorylation of cardiac cMyBP-C and cTnI in donor compared to the ISHD and IDCM sample. <bold>c</bold> The mean values are shown in the <italic>bar</italic> graph. Phosphorylation of cTnI was significantly higher in ISHD compared to IDCM. <bold>d</bold> A significant positive correlation was found between the phosphorylation status of cMyBP-C and cTnI (<italic>P</italic> < 0.0001; R<sup>2</sup> = 0.75). <italic>MHC</italic> myosin heavy chain, <italic>cMyBP-C</italic> cardiac myosin protein C, <italic>cTnT</italic> cardiac troponin T, <italic>cTnI</italic> cardiac Troponin I, <italic>MLC-2</italic> myosin light chain 2, <italic>M</italic> molecular weight marker (PeppermintStick Phosphoprotein marker in which ovalbumin (OV) and β-casein (β) are phosphorylated). *<italic>P</italic> < 0.05 in Bonferroni-post tests, IDCM versus ISHD; <sup>#</sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor</p></caption><graphic xlink:href="10974_2010_9231_Fig2_HTML" id="MO2"></graphic></fig></p><p>Higher PKA-mediated phosphorylation of cTnI (at Ser23 and Ser24, i.e., PKA sites) in ISHD compared to IDCM was confirmed in Western blotting (Fig. <xref rid="Fig3" ref-type="fig">3</xref>). Consistent with ProQ Diamond analysis of cTnI phosphorylation, the Western blots revealed significantly lower cTnI phosphorylation at PKA-sites in failing compared to donor.<fig id="Fig3"><label>Fig. 3</label><caption><p>Western blot analysis of troponin I (cTnI) phosphorylation at the PKA-sites Ser 23/24 revealed significantly higher cTnI phosphorylation in ISHD compared to IDCM, while cTnI phosphorylation was lower in both failing groups compared to donor. *<italic>P</italic> < 0.05 in Bonferroni-post tests, IDCM versus ISHD; <sup>#</sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor</p></caption><graphic xlink:href="10974_2010_9231_Fig3_HTML" id="MO3"></graphic></fig></p><p>Analysis of cTnI species separated by Phos-tag polyacrylamide gels revealed three bands upon staining of Western blots with a specific anti-cTnI antibody (8I-7) in donor, while only two bands were observed in the failing sample shown in Fig. <xref rid="Fig4" ref-type="fig">4</xref>a. The lower band was recognized by an antibody directed against cTnI unphosphorylated at PKA sites (22B11). The upper band was recognized by the phosphorylation-specific antibody which recognizes the PKA-sites Ser 23 and Ser 24. The second band on the blot is the mono-phosphorylated form of cTnI (Messer et al. <xref ref-type="bibr" rid="CR24">2009</xref>). Phos-tag analysis of samples from all groups are shown in Fig. <xref rid="Fig4" ref-type="fig">4</xref>b. The distribution of the cTnI forms was significantly different among the three groups (Fig. <xref rid="Fig4" ref-type="fig">4</xref>c). The unphosphorylated form was highest in IDCM, while the bisphosphorylated form was highest in donor. A significant correlation was observed between phosphorylated cTnI on Phos-tag and cTnI phosphorylation analyzed by ProQ Diamond (Fig. <xref rid="Fig4" ref-type="fig">4</xref>d; <italic>P</italic> < 0.0001; R<sup>2</sup> = 0.75).<fig id="Fig4"><label>Fig. 4</label><caption><p><bold>a</bold> Phos-tag analysis of troponin I (cTnI) species revealed three cTnI bands in donor, of which the lowest band stained with an antibody directed against non-phosphorylated cTnI (22B11), and the highest band stained with the antibody specific for cTnI phosphorylation at PKA sites Ser23 and Ser24. <bold>b</bold> Examples of cTnI species separated by Phos-tag analysis in different ISHD, IDCM and donor samples. <bold>c</bold> The distribution of cTnI species was significantly different among groups. <bold>d</bold> A significant correlation was observed between phosphorylated cTnI on Phos-tag and phosphorylated cTnI on Pro-Q Diamond-Stain (<italic>P</italic> < 0.0001; R<sup>2</sup> = 0.75). <sup>#</sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor</p></caption><graphic xlink:href="10974_2010_9231_Fig4_HTML" id="MO4"></graphic></fig></p><p>ProQ Diamond analysis also revealed higher phosphorylation of myosin light chain 2 (MLC-2) in ISHD compared to both IDCM and donor (Table <xref rid="Tab2" ref-type="table">2</xref>), while there were no significant differences in phosphorylation of the other myofilament proteins, desmin and troponin T (data not shown). The difference in MLC-2 phosphorylation may be in part explained by differences in PP-1 expression. Western blot analysis of PP-1 revealed significantly higher PP-1 expression in IDCM compared to ISHD and donor (Table <xref rid="Tab2" ref-type="table">2</xref>).</p><p>Western blot analysis showed increased phospholamban protein levels in IDCM and ISHD compared to donor and a significantly lower SERCA2a level in IDCM compared to both ISHD and donor (Table <xref rid="Tab2" ref-type="table">2</xref>). The ratio of phospholamban over SERCA2a significantly differed among groups and was highest in IDCM.</p></sec><sec id="Sec15"><title>Higher Ca<sup>2+</sup>-sensitivity in IDCM than in ISHD</title><p>Force measurements were performed in single cardiomyocytes isolated from 8 IDCM hearts (42 cardiomyocytes), 8 ISHD hearts (27 cardiomyocytes) and 8 donor hearts (41 cardiomyocytes). Cross-sectional area of the cardiomyocytes determined at a sarcomere length of 2.2 μm was significantly higher in IDCM (556 ± 44 μm<sup>2</sup>) and ISHD (690 ± 75 μm<sup>2</sup>) compared to donor (339 ± 26 μm<sup>2</sup>) (<italic>P</italic> < 0.05 in one-way ANOVA).</p><p>Maximal active tension (F<sub>active</sub>) did not differ (Fig. <xref rid="Fig5" ref-type="fig">5</xref>a), while passive tension (F<sub>passive</sub>) was significantly lower in IDCM and ISHD compared to donor (Fig. <xref rid="Fig5" ref-type="fig">5</xref>b). Noteworthy, myofilament pCa<sub>50</sub> was significantly lower in ISHD compared to IDCM (Fig. <xref rid="Fig5" ref-type="fig">5</xref>c, d). A significantly higher pCa<sub>50</sub> was found in failing heart compared to donor (Fig. <xref rid="Fig5" ref-type="fig">5</xref>c, d). Moreover, the steepness of the sigmoidal force-pCa relationship (nHill) was significantly higher in ISHD (4.05 ± 0.12) compared to IDCM (3.58 ± 0.10) and donor (3.70 ± 0.14). A monovariate linear regression analysis revealed a significant correlation between pCa<sub>50</sub> and phosphorylated cMyBP-C (<italic>P</italic> < 0.05; R<sup>2</sup> = 0.24) (Fig. <xref rid="Fig5" ref-type="fig">5</xref>e), while no significant correlation was found between pCa<sub>50</sub> and ProQ Diamond-analyzed phosphorylated cTnI (<italic>P</italic> = 0.09; R<sup>2</sup> = 0.12). Troponin I phosphorylation determined by Phos-tag analysis did significantly correlate with pCa<sub>50</sub> (<italic>P</italic> < 0.01; R<sup>2</sup> = 0.43) (Fig. <xref rid="Fig5" ref-type="fig">5</xref>f). The individual data per patient/donor for phosphorylation of the PKA target proteins, cMyBP-C and cTnI, and myofilament Ca<sup>2+</sup>-sensitivity are summarized in Table <xref rid="Tab1" ref-type="table">1</xref>.<fig id="Fig5"><label>Fig. 5</label><caption><p><bold>a</bold> F<sub>active</sub> did not differ among groups. <bold>b</bold> F<sub>passive</sub> was significantly lower in failing groups compared to donor. <bold>c</bold>, <bold>d</bold> pCa<sub>50</sub> was significantly higher in failing groups compared to donor. The pCa<sub>50</sub> was significantly lower in ISHD compared to IDCM. <bold>e</bold> A significant correlation was observed between pCa<sub>50</sub> and phosphorylated cMyBP-C (<italic>P</italic> < 0.05; R<sup>2</sup> = 0.24). <bold>f</bold> A significant correlation was also found between pCa<sub>50</sub> and Phos-tag analyzed cTnI phosphorylation (<italic>P</italic> < 0.01; R<sup>2</sup> = 0.43). *<italic>P</italic> < 0.05 in Bonferroni-post tests, IDCM versus ISHD; <sup>#</sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor</p></caption><graphic xlink:href="10974_2010_9231_Fig5_HTML" id="MO5"></graphic></fig></p></sec><sec id="Sec16"><title>Structural alterations</title><p>Representative examples of light microscopy and electron microscopy images of LV sections from the three groups are shown in Fig. <xref rid="Fig6" ref-type="fig">6</xref>a and b, respectively. Cardiomyocyte diameter did not differ between ISHD and IDCM, but was significantly higher than observed in donor (Fig. <xref rid="Fig6" ref-type="fig">6</xref>c). Collagen volume fraction was significantly higher in IDCM compared to ISHD. Moreover, collagen volume fraction was significantly higher in both failing compared to donor (Fig. <xref rid="Fig6" ref-type="fig">6</xref>d). No differences were found in myofibrillar density between ISHD and IDCM, while it was significantly lower in both failing compared to donor (Fig. <xref rid="Fig6" ref-type="fig">6</xref>e).<fig id="Fig6"><label>Fig. 6</label><caption><p>Light microscopy (<bold>a</bold>) (hematoxylin-eosin stained; scale 10 μm) and electron microscopy (<bold>b</bold>; 3600× magnification) images of left ventricular sections from the three groups. Bar graphs showing cardiomyocyte diameter (<bold>c</bold>), collagen volume fraction (<bold>d</bold>) and myofibrillar density (<bold>e</bold>). A significant increase was observed in cardiomyocyte diameter and collagen volume fraction in both failing groups compared to donor. Analysis of cardiomyocyte diameter and collagen volume fraction were performed in 9 ISHD, 8 IDCM and 5 donor hearts. In addition, a significantly lower myofibrillar density was present in failing groups compared to donor. Analysis of myofibrillar density was performed in 8 ISHD, 6 IDCM and 5 donor hearts. The collagen volume fraction in IDCM was significantly higher compared to ISHD. *<italic>P</italic> < 0.05 in Bonferroni-post tests, IDCM versus ISHD; <sup>#</sup><italic>P</italic> < 0.05, in Bonferroni-post tests, failing versus donor. <italic>Arrow</italic> to indicate collagen</p></caption><graphic xlink:href="10974_2010_9231_Fig6_HTML" id="MO6"></graphic></fig></p></sec></sec><sec id="Sec17"><title>Discussion</title><p>In the present study, diverse changes were found in the βAR pathway in IDCM and ISHD patients. The results indicate that there are differences in the cellular structure and function between both patient groups. Compared to ISHD, IDCM was characterized by a more severe receptor βAR down-regulation and increased G<sub>i</sub> expression, increased PP-1 expression, an enhanced reduction in protein phosphorylation, increased myofilament pCa<sub>50</sub>, reduced SERCA2a expression and higher collagen volume fraction. The data indicate that cellular dysfunction is more severe in IDCM than in ISHD patients.</p><sec id="Sec18"><title>Changes in components of the β-adrenergic pathway</title><p>In the present study, total βAR density was significantly reduced in IDCM compared to donor with intermediate values in ISHD. This down-regulation may have been caused by reduced mRNA levels (Hadcock and Malbon <xref ref-type="bibr" rid="CR16">1998</xref>). In addition, βAR may be degraded upon internalization of receptors, which is preceded by the process of receptor uncoupling (Wang and Dhalla <xref ref-type="bibr" rid="CR38">2000</xref>). The regulating step in the latter process is receptor phosphorylation, either by second-messenger activated kinases such as PKA, or by GRKs, which only phosphorylate agonist occupied receptors (Fig. <xref rid="Fig7" ref-type="fig">7</xref>). Both GRK2 and GRK5 are determinants of βAR responsiveness of the heart, as they disrupt the interaction between receptors and the heterotrimeric G proteins (Wang and Dhalla <xref ref-type="bibr" rid="CR38">2000</xref>). This process of receptor uncoupling is thought to be an important contributor to βAR desensitization and down-regulation due to increased sympathetic tone in cardiac disease. In failing human tissue, Ungerer et al. (<xref ref-type="bibr" rid="CR33">1993</xref>, <xref ref-type="bibr" rid="CR34">1994</xref>) showed increased GRK2 mRNA and activity in both ISHD and IDCM. In contrast, in the present study we observed lower GRK2 protein expression in both failing groups compared to donor, while GRK5 protein expression was significantly higher in ISHD compared to IDCM and donor.<fig id="Fig7"><label>Fig. 7</label><caption><p>Activation of β-adrenergic receptor pathway in the heart. Overall, changes were more severe in IDCM compared to ISHD, indicated by the <italic>dotted arrows</italic>, i.e., decrease or increase in IDCM compared to ISHD. <italic>P</italic> Phosphorylation, <italic>βAR</italic> β-adrenergic receptor, <italic>Gs</italic> G-stimulatory protein, <italic>Gi</italic> G-inhibitory protein, <italic>GRK</italic> G-coupled receptor kinase, <italic>Ca</italic><sup><italic>2+</italic></sup> calcium, <italic>ATP</italic> adenosine tri-phosphate, <italic>cAMP</italic> cyclic AMP, <italic>PKA</italic> Protein kinase A, <italic>PP-1</italic> protein phosphatase 1, <italic>MLC-2</italic> myosin light chain 2, <italic>cMyBP-C</italic> cardiac myosin binding protein C, <italic>cTnI</italic> cardiac troponin I, <italic>SERCA2a</italic> SR Ca<sup>2+</sup>ATPase</p></caption><graphic xlink:href="10974_2010_9231_Fig7_HTML" id="MO7"></graphic></fig></p><p>The discrepant observation in GRK5 between ISHD and IDCM may reflect a difference in severity of disease, as Leineweber et al. (<xref ref-type="bibr" rid="CR21">2005</xref>) observed an increase in GRK activity in right atrial tissue from patients at NYHA I and II, while in more severe stages (NYHA III and IV) GRK activity was similar as observed in controls. Interestingly, βAR density did not differ in NYHA I and II and was significantly reduced compared to controls in NYHA III and IV. These data are suggestive for a transient increase in GRK activity during the course of heart failure, and indicate that increases in GRK precede receptor down-regulation in the human heart. Accordingly, the high GRK5 expression and the lower reduction in βAR density in ISHD compared to IDCM observed in the present study may reflect a less severe disease stage in ISHD, despite similar NYHA classification. The latter is further supported by the significantly higher expression of inhibitor G-protein in IDCM compared to ISHD.</p></sec><sec id="Sec19"><title>More severe cellular phenotype in IDCM compared to ISHD</title><p>Analysis of sarcomeric protein phosphorylation revealed significant differences in the βAR target proteins cMyBP-C and cTnI. Consistent with previous studies (El-Armouche et al. <xref ref-type="bibr" rid="CR13">2007</xref>; van der Velden et al. <xref ref-type="bibr" rid="CR35">2003</xref>; Messer et al. <xref ref-type="bibr" rid="CR23">2007</xref>, <xref ref-type="bibr" rid="CR24">2009</xref>; Copeland et al. <xref ref-type="bibr" rid="CR12">2010</xref>) phosphorylation of cMyBP-C and cTnI was significantly lower in both failing groups compared to donor, which has been explained by reduced PKA-mediated phosphorylation due to βAR desensitization and down-regulation in cardiac disease (Wolff et al. <xref ref-type="bibr" rid="CR40">1996</xref>; van der Velden et al. <xref ref-type="bibr" rid="CR35">2003</xref>). Noteworthy, cMyBP-C and cTnI phosphorylation was lower in IDCM compared to ISHD, which fits the larger reduction in βAR density and larger increase in G<sub>αi-1</sub> expression observed in IDCM compared to ISHD. The higher myofilament pCa<sub>50</sub> in IDCM compared to ISHD may be well explained by the significantly lower (PKA-mediated) myofilament protein phosphorylation observed in IDCM.</p><p>Interestingly, analysis of cTnI species using Phos-tag polyacrylamide gels showed that the difference in cTnI phosphorylation between IDCM and donor can be largely explained by a difference in the bis-phosphorylated form of cTnI (Fig. <xref rid="Fig4" ref-type="fig">4</xref>c). It is tempting to speculate that a difference in cTnI phosphorylation at PKA sites Ser 23/24 underlies the differences in pCa<sub>50</sub> among groups. Although a significant correlation was found between myofilament pCa<sub>50</sub> and phosphorylation status of cMyBP-C (Fig. <xref rid="Fig5" ref-type="fig">5</xref>e), the correlation with ProQ Diamond assessed cTnI phosphorylation did not reach statistical significance (<italic>P</italic> = 0.09). Noteworthy, cTnI phosphorylation determined with the Phos-tag assay did significantly correlate with myofilament Ca<sup>2+</sup>-sensitivity (Fig. <xref rid="Fig5" ref-type="fig">5</xref>f), indicating that Phos-tag analysis is a very accurate method to determine cTnI phosphorylation.</p><p>The correlation between cMyBP-C phosphorylation and pCa<sub>50</sub> was stronger when cMyBP-C phosphorylation was combined with ProQ-Diamond assessed cTnI phosphorylation (<italic>P</italic> = <0.05; R<sup>2</sup> = 0.27; not shown). In a recent study in human myocardium we showed that myofibrillar targets of PKA, cMyBP-C and/or titin, play an important role in modulating the effect of cTnI phosphorylation on pCa<sub>50</sub> in human myocardium (Kooij et al. <xref ref-type="bibr" rid="CR19">2010</xref>). Exchange of endogenous (mostly unphosphorylated) cTnI with PKA-phosphorylated troponin complex did not reduce pCa<sub>50</sub> in failing cardiomyocytes, in which endogenous cMyBP-C phosphorylation is low. Accordingly, our present data are compatible with a modulatory role for cMyBP-C in force development at submaximal calcium concentrations in human myocardium.</p><p>In addition to the PKA targets, cTnI and cMyBP-C, phosphorylation of MLC-2 was significantly lower in IDCM than in ISHD. Dephosphorylation of MLC-2 occurs via PP-1, which was significantly higher in IDCM compared to ISHD. Although increased PP-1 expression may explain the relatively low MLC-2 phosphorylation in IDCM, it cannot explain the significantly lower MLC-2 phosphorylation in donor compared to ISHD, as PP-1 expression tended to be even lower in donor compared to ISHD. Other kinases/phosphatases most likely underlie the differences in MLC-2 phosphorylation observed between ISHD and donor myocardium and warrant future research.</p><p>Moreover, upon activation of βAR, PP-1 activity is depressed by PKA via phosphorylation of protein inhibitor 1 (I1) (Neumann et al. <xref ref-type="bibr" rid="CR28">1991</xref>). Thus, apart from increased PP-1 expression, perturbations in βAR signaling will increase activity of PP-1, which may explain the lower MLC-2 phosphorylation in IDCM compared to ISHD. Increased activity and mRNA level of PP-1 has been reported previously in human IDCM (Neumann et al. <xref ref-type="bibr" rid="CR29">1997</xref>). Increased activity of PP-1 in a transgenic mouse model resulted in decreased myocardial contractility and dilated cardiomyopathy underscoring a detrimental role for PP-1 in heart failure (Carr et al. <xref ref-type="bibr" rid="CR8">2002</xref>). Increased PP-1 will also impair Ca<sup>2+</sup>-handling by dephosphorylation of phospholamban. The resulting reduction in SR Ca<sup>2+</sup> loading will be enhanced further by the reduction in SERCA2a expression in IDCM. Although several studies did not find differences in SERCA2a and PLB at mRNA levels between ISHD and IDCM (Arai et al. <xref ref-type="bibr" rid="CR2">1993</xref>; Flesch et al. <xref ref-type="bibr" rid="CR15">1996</xref>), our study showed reduced SERCA2a protein expression in IDCM, and increased phospholamban expression in both failing groups. Higher PP-1 expression and lower SERCA2a expression are indicative for a more severe cellular phenotype in patients with IDCM.</p><p>In line with previous studies (Anversa et al. <xref ref-type="bibr" rid="CR1">1986</xref>; Parodi et al. <xref ref-type="bibr" rid="CR32">1993</xref>; Weber <xref ref-type="bibr" rid="CR39">1989</xref>) we observed three structural alterations in end-stage heart failure: increased cardiomyocyte diameter (Fig. <xref rid="Fig6" ref-type="fig">6</xref>c), increased collagen volume fraction (Fig. <xref rid="Fig6" ref-type="fig">6</xref>d) and decreased myofibrillar density (Fig. <xref rid="Fig6" ref-type="fig">6</xref>e). While no difference was found in cardiomyocyte diameter and myofibrillar density between IDCM and ISHD, collagen volume fraction was significantly higher in IDCM compared to ISHD, which is in line with a previous study by Parodi et al. (<xref ref-type="bibr" rid="CR32">1993</xref>).</p></sec><sec id="Sec20"><title>Adaptive cellular mechanism</title><p>In agreement with previous studies (Makarenko et al. <xref ref-type="bibr" rid="CR22">2004</xref>; Nagueh et al. <xref ref-type="bibr" rid="CR26">2004</xref>; Neagoe et al. <xref ref-type="bibr" rid="CR27">2002</xref>) F<sub>passive</sub> in end-stage human heart failure was lower in comparison to donor. It has been proposed that the reduction in F<sub>passive</sub> is due to a shift in titin isoform composition, from the stiff N2B to the more compliant N2BA isoform (Makarenko et al. <xref ref-type="bibr" rid="CR22">2004</xref>; Nagueh et al. <xref ref-type="bibr" rid="CR26">2004</xref>). In contrast, enhanced F<sub>passive</sub> was found in patients with less severe forms of heart failure (NYHA II-III) (Borbély et al. <xref ref-type="bibr" rid="CR5">2005</xref>, <xref ref-type="bibr" rid="CR6">2009</xref>; van Heerebeek et al. <xref ref-type="bibr" rid="CR36">2006</xref>), in which a similar shift in titin isoform composition was found as observed in end-stage heart failure (i.e., more compliant isoform). The increased F<sub>passive</sub> at an early phase of heart failure was related with relative hypophosphorylation of the stiff N2B titin isoform (Borbély et al. <xref ref-type="bibr" rid="CR6">2009</xref>). Cardiomyocyte stiffness reflects the balance between isoform composition and isoform-specific phosphorylation status of titin. The shift to the compliant N2BA isoform during heart failure seems to be an adaptive mechanism to lower passive force (Makarenko et al. <xref ref-type="bibr" rid="CR22">2004</xref>), which may be maximal at end-stage heart failure.</p></sec></sec><sec id="Sec21"><title>Conclusions</title><p>Comparison of myocardium from patients with ISHD and IDCM end-stage HF revealed more severe cellular perturbations in patients with IDCM which are summarized in Fig. <xref rid="Fig7" ref-type="fig">7</xref>. Our data support previous studies in which transient changes were observed in the βAR pathway. Increased GRK expression may be a primary event and possibly precedes the reduction in βAR density, and the changes in expression of proteins involved in calcium handling and PP1. Noteworthy, Leineweber et al. (<xref ref-type="bibr" rid="CR21">2005</xref>) showed that GRK5 was significantly lower in patients treated with β-blockers only in the relatively early stages of heart failure (i.e., NYHA I and II), in which GRK5 was higher compared to the end-stage of HF. Hence, the response to current treatment may depend on cause of cardiac disease, and may be less in patients with IDCM.</p></sec></body><back><ack><title>Conflict of Interest</title><p>None.</p><p><bold>Open Access</bold> This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.</p></ack><ref-list id="Bib1"><title>References</title><ref id="CR1"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Anversa</surname><given-names>P</given-names></name><name><surname>Ricci</surname><given-names>R</given-names></name><name><surname>Olivetti</surname><given-names>G</given-names></name></person-group><article-title>Quantitative structural analysis of the myocardium during physiologic growth and induced cardiac hypertrophy: a review</article-title><source>J Am Coll Cardiol</source><year>1986</year><volume>36</volume><issue>7</issue><fpage>1140</fpage><lpage>1149</lpage><pub-id pub-id-type="doi">10.1016/S0735-1097(86)80236-4</pub-id><pub-id pub-id-type="pmid">2937828</pub-id></mixed-citation></ref><ref id="CR2"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Arai</surname><given-names>M</given-names></name><name><surname>Alpert</surname><given-names>NR</given-names></name><name><surname>Mac Lennan</surname><given-names>DH</given-names></name><name><surname>Barton</surname><given-names>P</given-names></name><name><surname>Petiasamy</surname><given-names>M</given-names></name></person-group><article-title>Alterations in sarcoplasmic reticulum gene expression in human heart failure a possible mechanism for alterations in systolic and diastolic properties of the failing myocardium</article-title><source>Circ Res</source><year>1993</year><volume>72</volume><issue>2</issue><fpage>463</fpage><lpage>469</lpage><pub-id pub-id-type="pmid">8418995</pub-id></mixed-citation></ref><ref id="CR3"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bers</surname><given-names>DM</given-names></name></person-group><article-title>Cardiac excitation-contraction coupling</article-title><source>Nature</source><year>2002</year><volume>415</volume><issue>6868</issue><fpage>198</fpage><lpage>205</lpage><pub-id pub-id-type="doi">10.1038/415198a</pub-id><pub-id pub-id-type="pmid">11805843</pub-id></mixed-citation></ref><ref id="CR4"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bohm</surname><given-names>M</given-names></name><name><surname>Maack</surname><given-names>C</given-names></name></person-group><article-title>Treatment of heart failure with beta-blockers</article-title><source>Bas Res Cardiol</source><year>2000</year><volume>95</volume><fpage>I15</fpage><lpage>I24</lpage><pub-id pub-id-type="doi">10.1007/s003950070004</pub-id></mixed-citation></ref><ref id="CR5"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Borbély</surname><given-names>A</given-names></name><name><surname>Velden</surname><given-names>J</given-names></name><name><surname>Papp</surname><given-names>Z</given-names></name><name><surname>Bronzwaer</surname><given-names>JG</given-names></name><name><surname>Edes</surname><given-names>I</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name><name><surname>Paulus</surname><given-names>WJ</given-names></name></person-group><article-title>Cardiomyocyte stiffness in diastolic heart failure</article-title><source>Circulation</source><year>2005</year><volume>111</volume><issue>6</issue><fpage>774</fpage><lpage>781</lpage><pub-id pub-id-type="doi">10.1161/01.CIR.0000155257.33485.6D</pub-id><pub-id pub-id-type="pmid">15699264</pub-id></mixed-citation></ref><ref id="CR6"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Borbély</surname><given-names>A</given-names></name><name><surname>Falcao-Pires</surname><given-names>I</given-names></name><name><surname>Heerebeek</surname><given-names>L</given-names></name><name><surname>Hamdani</surname><given-names>N</given-names></name><name><surname>Edes</surname><given-names>I</given-names></name><name><surname>Gavina</surname><given-names>C</given-names></name><name><surname>Leite-Moreira</surname><given-names>AF</given-names></name><name><surname>Bronzwaer</surname><given-names>JG</given-names></name><name><surname>Papp</surname><given-names>Z</given-names></name><name><surname>Velden</surname><given-names>J</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name><name><surname>Paulus</surname><given-names>WJ</given-names></name></person-group><article-title>Hypophosphorylation of the Stiff N2B titin isoform raises cardiomyocyte resting tension in failing human myocardium</article-title><source>Circ Res</source><year>2009</year><volume>104</volume><issue>6</issue><fpage>780</fpage><lpage>786</lpage><pub-id pub-id-type="doi">10.1161/CIRCRESAHA.108.193326</pub-id><pub-id pub-id-type="pmid">19179657</pub-id></mixed-citation></ref><ref id="CR7"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Brodde</surname><given-names>OE</given-names></name><name><surname>Michel</surname><given-names>MC</given-names></name></person-group><article-title>Adrenergic and muscarinic receptors in the human heart</article-title><source>Pharmacol Rev</source><year>1999</year><volume>51</volume><issue>4</issue><fpage>651</fpage><lpage>690</lpage><pub-id pub-id-type="pmid">10581327</pub-id></mixed-citation></ref><ref id="CR8"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Carr</surname><given-names>AN</given-names></name><name><surname>Schmidt</surname><given-names>AG</given-names></name><name><surname>Suzuki</surname><given-names>Y</given-names></name><name><surname>del Monte</surname><given-names>F</given-names></name><name><surname>Sato</surname><given-names>Y</given-names></name><name><surname>Lanner</surname><given-names>C</given-names></name><name><surname>Breeden</surname><given-names>K</given-names></name><name><surname>Jing</surname><given-names>SL</given-names></name><name><surname>Allen</surname><given-names>PB</given-names></name><name><surname>Greengard</surname><given-names>P</given-names></name><name><surname>Yatani</surname><given-names>A</given-names></name><name><surname>Hoit</surname><given-names>BD</given-names></name><name><surname>Grupp</surname><given-names>IL</given-names></name><name><surname>Hajjar</surname><given-names>RJ</given-names></name><name><surname>DePaoli-Roach</surname><given-names>AA</given-names></name><name><surname>Kranias</surname><given-names>EG</given-names></name></person-group><article-title>Type 1 phosphatase a negative regulator of cardiac function</article-title><source>Mol Cell Biol</source><year>2002</year><volume>22</volume><issue>12</issue><fpage>4124</fpage><lpage>4135</lpage><pub-id pub-id-type="doi">10.1128/MCB.22.12.4124-4135.2002</pub-id><pub-id pub-id-type="pmid">12024026</pub-id></mixed-citation></ref><ref id="CR9"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cheng</surname><given-names>Y</given-names></name><name><surname>Prusoff</surname><given-names>WH</given-names></name></person-group><article-title>Relationship between the inhibition constant (<italic>K</italic>i) and the concentration of an inhibitor, which causes 50 per cent inhibition (I<sub>50</sub>) of an enzymatic reaction</article-title><source>Biochem Pharmacol</source><year>1973</year><volume>22</volume><issue>23</issue><fpage>3099</fpage><lpage>3108</lpage><pub-id pub-id-type="doi">10.1016/0006-2952(73)90196-2</pub-id><pub-id pub-id-type="pmid">4202581</pub-id></mixed-citation></ref><ref id="CR10"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cho</surname><given-names>H</given-names></name><name><surname>Kehrl</surname><given-names>JH</given-names></name></person-group><article-title>Localization of Gi alpha proteins in the centrosomes and at the midbody: implication for their role in cell division</article-title><source>J Cell Biol</source><year>2007</year><volume>178</volume><issue>2</issue><fpage>245</fpage><lpage>255</lpage><pub-id pub-id-type="doi">10.1083/jcb.200604114</pub-id><pub-id pub-id-type="pmid">17635935</pub-id></mixed-citation></ref><ref id="CR11"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cohn</surname><given-names>JN</given-names></name><name><surname>Levine</surname><given-names>TB</given-names></name><name><surname>Olivari</surname><given-names>MT</given-names></name><name><surname>Garberg</surname><given-names>V</given-names></name><name><surname>Lura</surname><given-names>D</given-names></name><name><surname>Francis</surname><given-names>GS</given-names></name><name><surname>Simon</surname><given-names>AB</given-names></name><name><surname>Rector</surname><given-names>T</given-names></name></person-group><article-title>Plasma norepinephrine as a guide to prognosis in patients with chronic congestive heart failure</article-title><source>N Engl J Med</source><year>1984</year><volume>311</volume><issue>13</issue><fpage>819</fpage><lpage>823</lpage><pub-id pub-id-type="doi">10.1056/NEJM198409273111303</pub-id><pub-id pub-id-type="pmid">6382011</pub-id></mixed-citation></ref><ref id="CR12"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Copeland</surname><given-names>O</given-names></name><name><surname>Sadayappan</surname><given-names>S</given-names></name><name><surname>Messer</surname><given-names>AE</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name><name><surname>Velden</surname><given-names>J</given-names></name><name><surname>Marston</surname><given-names>SB</given-names></name></person-group><article-title>Analysis of cardiac myosin binding protein C in human heart muscle</article-title><source>J Mol Cell Cardiol</source><year>2010</year><volume>49</volume><fpage>1003</fpage><lpage>1011</lpage><pub-id pub-id-type="doi">10.1016/j.yjmcc.2010.09.007</pub-id><pub-id pub-id-type="pmid">20850451</pub-id></mixed-citation></ref><ref id="CR13"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>El-Armouche</surname><given-names>A</given-names></name><name><surname>Pohlmann</surname><given-names>L</given-names></name><name><surname>Schlossarek</surname><given-names>S</given-names></name><name><surname>Starbatty</surname><given-names>J</given-names></name><name><surname>Yeh</surname><given-names>YH</given-names></name><name><surname>Nattel</surname><given-names>S</given-names></name><name><surname>Dobrev</surname><given-names>D</given-names></name><name><surname>Eschenhagen</surname><given-names>T</given-names></name><name><surname>Carrier</surname><given-names>L</given-names></name></person-group><article-title>Decreased phosphorylation levels of cardiac myosin-binding protein-C in human and experimental heart failure</article-title><source>J Mol Cell Cardiol</source><year>2007</year><volume>43</volume><issue>2</issue><fpage>223</fpage><lpage>229</lpage><pub-id pub-id-type="doi">10.1016/j.yjmcc.2007.05.003</pub-id><pub-id pub-id-type="pmid">17560599</pub-id></mixed-citation></ref><ref id="CR14"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Elliott</surname><given-names>P</given-names></name><name><surname>Andersson</surname><given-names>B</given-names></name><name><surname>Arbustini</surname><given-names>E</given-names></name><name><surname>Bilinska</surname><given-names>Z</given-names></name><name><surname>Cecchi</surname><given-names>F</given-names></name><name><surname>Charron</surname><given-names>P</given-names></name><name><surname>Dubourg</surname><given-names>O</given-names></name><name><surname>Kuhl</surname><given-names>U</given-names></name><name><surname>Maisch</surname><given-names>B</given-names></name><name><surname>McKenna</surname><given-names>WJ</given-names></name><name><surname>Monserrat</surname><given-names>L</given-names></name><name><surname>Pankuweit</surname><given-names>S</given-names></name><name><surname>Rapezzi</surname><given-names>C</given-names></name><name><surname>Seferovic</surname><given-names>P</given-names></name><name><surname>Tavazzi</surname><given-names>L</given-names></name><name><surname>Keren</surname><given-names>A</given-names></name></person-group><article-title>Classification of the cardiomyopathies: a position statement from the European society of cardiology working group on myocardial and pericardial diseases</article-title><source>Eur Heart J</source><year>2008</year><volume>29</volume><fpage>270</fpage><lpage>276</lpage><pub-id pub-id-type="doi">10.1093/eurheartj/ehm342</pub-id><pub-id pub-id-type="pmid">17916581</pub-id></mixed-citation></ref><ref id="CR15"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Flesch</surname><given-names>M</given-names></name><name><surname>Schwinger</surname><given-names>RH</given-names></name><name><surname>Schnabel</surname><given-names>P</given-names></name><name><surname>Schiffer</surname><given-names>F</given-names></name><name><surname>Gelder</surname><given-names>I</given-names></name><name><surname>Bavendiek</surname><given-names>U</given-names></name><name><surname>Südkamp</surname><given-names>M</given-names></name><name><surname>Kuhn-Regnier</surname><given-names>F</given-names></name><name><surname>Böhm</surname><given-names>M</given-names></name></person-group><article-title>Sarcoplasmic reticulum Ca<sup>2+</sup>-ATPase and phospholamban mRNA and protein levels in end-stage heart failure due to ischemic or dilated cardiomyopathy</article-title><source>J Mol Med</source><year>1996</year><volume>74</volume><issue>6</issue><fpage>321</fpage><lpage>332</lpage><pub-id pub-id-type="doi">10.1007/BF00207509</pub-id><pub-id pub-id-type="pmid">8862513</pub-id></mixed-citation></ref><ref id="CR16"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hadcock</surname><given-names>JR</given-names></name><name><surname>Malbon</surname><given-names>CC</given-names></name></person-group><article-title>Down-regulation of β-adrenergic receptors: agonist-induced reduction in receptor mRNA levels</article-title><source>Proc Natl Acad Sci USA</source><year>1998</year><volume>85</volume><issue>14</issue><fpage>5021</fpage><lpage>5025</lpage><pub-id pub-id-type="doi">10.1073/pnas.85.14.5021</pub-id><pub-id pub-id-type="pmid">2899321</pub-id></mixed-citation></ref><ref id="CR17"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kentish</surname><given-names>JC</given-names></name><name><surname>McCloskey</surname><given-names>DT</given-names></name><name><surname>Layland</surname><given-names>J</given-names></name><name><surname>Palmer</surname><given-names>S</given-names></name><name><surname>Leiden</surname><given-names>JM</given-names></name><name><surname>Martin</surname><given-names>AF</given-names></name><name><surname>Solaro</surname><given-names>RJ</given-names></name></person-group><article-title>Phosphorylation of troponin I by protein kinase A accelerates relaxation and crossbridge cycle kinetics in mouse ventricular muscle</article-title><source>Circ Res</source><year>2001</year><volume>88</volume><issue>10</issue><fpage>1059</fpage><lpage>1065</lpage><pub-id pub-id-type="doi">10.1161/hh1001.091640</pub-id><pub-id pub-id-type="pmid">11375276</pub-id></mixed-citation></ref><ref id="CR18"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kinoshota</surname><given-names>E</given-names></name><name><surname>Kinoshita-Kikuta</surname><given-names>E</given-names></name><name><surname>Takiyama</surname><given-names>K</given-names></name><name><surname>Koike</surname><given-names>T</given-names></name></person-group><article-title>Phosphate-binding tag, a new tool to visualize phosphorylated proteins</article-title><source>Mol Cell Proteomics</source><year>2006</year><volume>5</volume><issue>4</issue><fpage>749</fpage><lpage>757</lpage><pub-id pub-id-type="pmid">16340016</pub-id></mixed-citation></ref><ref id="CR19"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kooij</surname><given-names>V</given-names></name><name><surname>Saes</surname><given-names>M</given-names></name><name><surname>Jaquet</surname><given-names>K</given-names></name><name><surname>Zaremba</surname><given-names>R</given-names></name><name><surname>Foster</surname><given-names>DB</given-names></name><name><surname>Murphy</surname><given-names>AM</given-names></name><name><surname>Remedios</surname><given-names>C</given-names></name><name><surname>Velden</surname><given-names>J</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name></person-group><article-title>Effect of troponin I Ser23/24 phosphorylation on Ca<sup>2+</sup>-sensitivity in human myocardium depends on the phosphorylation background</article-title><source>J Mol Cell Cardiol</source><year>2010</year><volume>48</volume><issue>5</issue><fpage>954</fpage><lpage>963</lpage><pub-id pub-id-type="doi">10.1016/j.yjmcc.2010.01.002</pub-id><pub-id pub-id-type="pmid">20079747</pub-id></mixed-citation></ref><ref id="CR20"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kranias</surname><given-names>EG</given-names></name><name><surname>Garvey</surname><given-names>JL</given-names></name><name><surname>Srivastava</surname><given-names>RD</given-names></name><name><surname>Solaro</surname><given-names>RJ</given-names></name></person-group><article-title>Phosphorylation and functional modifications of sarcoplasmic reticulum and myofibrils in isolated rabbit hearts stimulated with isoprenaline</article-title><source>Biochem J</source><year>1985</year><volume>226</volume><issue>1</issue><fpage>113</fpage><lpage>121</lpage><pub-id pub-id-type="pmid">3156585</pub-id></mixed-citation></ref><ref id="CR21"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Leineweber</surname><given-names>K</given-names></name><name><surname>Rohe</surname><given-names>P</given-names></name><name><surname>Beilfuss</surname><given-names>A</given-names></name><name><surname>Wolf</surname><given-names>C</given-names></name><name><surname>Sporkmann</surname><given-names>H</given-names></name><name><surname>Bruck</surname><given-names>H</given-names></name><name><surname>Jakob</surname><given-names>HG</given-names></name><name><surname>Heusch</surname><given-names>G</given-names></name><name><surname>Philipp</surname><given-names>T</given-names></name><name><surname>Brodde</surname><given-names>OE</given-names></name></person-group><article-title>G-protein-coupled receptor kinase activity in human heart failure: effects of beta-adrenoceptor blockade</article-title><source>Cardiovasc Res</source><year>2005</year><volume>66</volume><issue>3</issue><fpage>512</fpage><lpage>519</lpage><pub-id pub-id-type="doi">10.1016/j.cardiores.2005.01.025</pub-id><pub-id pub-id-type="pmid">15914116</pub-id></mixed-citation></ref><ref id="CR22"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Makarenko</surname><given-names>I</given-names></name><name><surname>Opitz</surname><given-names>CA</given-names></name><name><surname>Leake</surname><given-names>MC</given-names></name><name><surname>Neagoe</surname><given-names>C</given-names></name><name><surname>Kulke</surname><given-names>M</given-names></name><name><surname>Gwathmey</surname><given-names>JK</given-names></name><name><surname>Monte</surname><given-names>F</given-names></name><name><surname>Hajjar</surname><given-names>RJ</given-names></name><name><surname>Linke</surname><given-names>WA</given-names></name></person-group><article-title>Passive stiffness changes caused by upregulation of compliant titin isoforms in human dilated cardiomyopathy hearts</article-title><source>Circ Res</source><year>2004</year><volume>95</volume><issue>7</issue><fpage>708</fpage><lpage>716</lpage><pub-id pub-id-type="doi">10.1161/01.RES.0000143901.37063.2f</pub-id><pub-id pub-id-type="pmid">15345656</pub-id></mixed-citation></ref><ref id="CR23"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Messer</surname><given-names>AE</given-names></name><name><surname>Jacques</surname><given-names>AM</given-names></name><name><surname>Marston</surname><given-names>SB</given-names></name></person-group><article-title>Troponin phosphorylation and regulatory function in human heart muscle: dephosphorylation of ser 23/24 on Troponin I could account for contractile defect in end-stage heart failure</article-title><source>J Mol Cell Cardiol</source><year>2007</year><volume>42</volume><fpage>247</fpage><lpage>259</lpage><pub-id pub-id-type="doi">10.1016/j.yjmcc.2006.08.017</pub-id><pub-id pub-id-type="pmid">17081561</pub-id></mixed-citation></ref><ref id="CR24"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Messer</surname><given-names>AE</given-names></name><name><surname>Gallon</surname><given-names>CE</given-names></name><name><surname>McKenna</surname><given-names>WJ</given-names></name><name><surname>Remedios</surname><given-names>CG</given-names></name><name><surname>Marston</surname><given-names>SB</given-names></name></person-group><article-title>The use of phosphate-affinity SDS-PAGE to measure the cardiac troponin I phosphorylation site distribution in human heart muscle</article-title><source>Proteomics Clin Appl</source><year>2009</year><volume>3</volume><fpage>1371</fpage><lpage>1382</lpage><pub-id pub-id-type="pmid">21136957</pub-id></mixed-citation></ref><ref id="CR25"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Muller</surname><given-names>A</given-names></name><name><surname>Linden</surname><given-names>GC</given-names></name><name><surname>Zuidwijk</surname><given-names>MJ</given-names></name><name><surname>Simonides</surname><given-names>WS</given-names></name><name><surname>Laarse</surname><given-names>WJ</given-names></name><name><surname>Hardeveld</surname><given-names>C</given-names></name></person-group><article-title>Differential effects of thyroid hormone on the expression of sarcoplasmic reticulum Ca<sup>2+</sup>-ATPase isoforms in rat skeletal muscle fibers</article-title><source>Biochem Biophys Res Commun</source><year>1991</year><volume>203</volume><issue>2</issue><fpage>35</fpage><lpage>40</lpage></mixed-citation></ref><ref id="CR26"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Nagueh</surname><given-names>SF</given-names></name><name><surname>Shah</surname><given-names>G</given-names></name><name><surname>Wu</surname><given-names>Y</given-names></name><name><surname>Torre-Amione</surname><given-names>G</given-names></name><name><surname>King</surname><given-names>NM</given-names></name><name><surname>Lahmers</surname><given-names>S</given-names></name><name><surname>Witt</surname><given-names>CC</given-names></name><name><surname>Becker</surname><given-names>K</given-names></name><name><surname>Labeit</surname><given-names>S</given-names></name><name><surname>Granzier</surname><given-names>HL</given-names></name></person-group><article-title>Altered titin expression, myocardial stiffness, and left ventricular function in patients with dilated cardiomyopathy</article-title><source>Circulation</source><year>2004</year><volume>110</volume><issue>2</issue><fpage>155</fpage><lpage>162</lpage><pub-id pub-id-type="doi">10.1161/01.CIR.0000135591.37759.AF</pub-id><pub-id pub-id-type="pmid">15238456</pub-id></mixed-citation></ref><ref id="CR27"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Neagoe</surname><given-names>C</given-names></name><name><surname>Kulke</surname><given-names>M</given-names></name><name><surname>Monte</surname><given-names>F</given-names></name><name><surname>Gwathmey</surname><given-names>JK</given-names></name><name><surname>Tombe</surname><given-names>PP</given-names></name><name><surname>Hajjar</surname><given-names>RJ</given-names></name><name><surname>Linke</surname><given-names>WA</given-names></name></person-group><article-title>Titin isoform switch in ischemic human heart disease</article-title><source>Circulation</source><year>2002</year><volume>106</volume><fpage>1333</fpage><lpage>1341</lpage><pub-id pub-id-type="doi">10.1161/01.CIR.0000029803.93022.93</pub-id><pub-id pub-id-type="pmid">12221049</pub-id></mixed-citation></ref><ref id="CR28"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Neumann</surname><given-names>J</given-names></name><name><surname>Gupta</surname><given-names>RC</given-names></name><name><surname>Schmitz</surname><given-names>W</given-names></name><name><surname>Scholz</surname><given-names>H</given-names></name><name><surname>Nairn</surname><given-names>AC</given-names></name><name><surname>Watanabe</surname><given-names>AM</given-names></name></person-group><article-title>Evidence for isoproterenol-induced phosphorylation of phosphatase inhibitor-1 in the intact heart</article-title><source>Circ Res</source><year>1991</year><volume>69</volume><issue>6</issue><fpage>1450</fpage><lpage>1457</lpage><pub-id pub-id-type="pmid">1659500</pub-id></mixed-citation></ref><ref id="CR29"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Neumann</surname><given-names>J</given-names></name><name><surname>Eschenhagen</surname><given-names>T</given-names></name><name><surname>Jones</surname><given-names>LR</given-names></name><name><surname>Linck</surname><given-names>B</given-names></name><name><surname>Schmitz</surname><given-names>W</given-names></name><name><surname>Scholz</surname><given-names>H</given-names></name><name><surname>Zimmermann</surname><given-names>N</given-names></name></person-group><article-title>Increased expression of cardiac phosphatases in patients with end-stage heart failure</article-title><source>J Mol Cell Cardiol</source><year>1997</year><volume>29</volume><issue>6</issue><fpage>265</fpage><lpage>272</lpage><pub-id pub-id-type="doi">10.1006/jmcc.1996.0271</pub-id><pub-id pub-id-type="pmid">9040041</pub-id></mixed-citation></ref><ref id="CR30"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Niclauss</surname><given-names>N</given-names></name><name><surname>Michel-Reher</surname><given-names>MB</given-names></name><name><surname>Alewijnse</surname><given-names>AE</given-names></name><name><surname>Michel</surname><given-names>MC</given-names></name></person-group><article-title>Comparison of three radioligands for the labelling of human β-adrenoceptor subtypes</article-title><source>Naunyn-Schmiedeberg’s Arch Pharmacol</source><year>2006</year><volume>374</volume><issue>3</issue><fpage>99</fpage><lpage>105</lpage><pub-id pub-id-type="doi">10.1007/s00210-006-0104-z</pub-id></mixed-citation></ref><ref id="CR31"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Packer</surname><given-names>M</given-names></name></person-group><article-title>Evolution of the neurohormonal hypothesis to explain the progression of chronic heart failure</article-title><source>Eur Heart J</source><year>1995</year><volume>16</volume><fpage>F4</fpage><lpage>F6</lpage></mixed-citation></ref><ref id="CR32"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Parodi</surname><given-names>O</given-names></name><name><surname>Maria</surname><given-names>R</given-names></name><name><surname>Oltrona</surname><given-names>L</given-names></name><name><surname>Testa</surname><given-names>R</given-names></name><name><surname>Sambuceti</surname><given-names>G</given-names></name><name><surname>Roghi</surname><given-names>A</given-names></name><name><surname>Merli</surname><given-names>M</given-names></name><name><surname>Belingheri</surname><given-names>L</given-names></name><name><surname>Accinni</surname><given-names>R</given-names></name><name><surname>Spinelli</surname><given-names>F</given-names></name></person-group><article-title>Myocardial blood flow distribution in patients with ischemic heart disease or dilated cardiomyopathy undergoing heart transplantation</article-title><source>Circulation</source><year>1993</year><volume>88</volume><issue>2</issue><fpage>509</fpage><lpage>522</lpage><pub-id pub-id-type="pmid">8339413</pub-id></mixed-citation></ref><ref id="CR33"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Ungerer</surname><given-names>M</given-names></name><name><surname>Böhm</surname><given-names>M</given-names></name><name><surname>Elce</surname><given-names>JS</given-names></name><name><surname>Erdmann</surname><given-names>E</given-names></name><name><surname>Lohse</surname><given-names>MJ</given-names></name></person-group><article-title>Altered expression of beta-adrenergic receptor kinase and beta 1-adrenergic receptors in the failing human heart</article-title><source>Circulation</source><year>1993</year><volume>87</volume><issue>2</issue><fpage>652</fpage><lpage>654</lpage><pub-id pub-id-type="pmid">8381061</pub-id></mixed-citation></ref><ref id="CR34"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Ungerer</surname><given-names>M</given-names></name><name><surname>Parruti</surname><given-names>G</given-names></name><name><surname>Böhm</surname><given-names>M</given-names></name><name><surname>Puzicha</surname><given-names>M</given-names></name><name><surname>DeBlasi</surname><given-names>A</given-names></name><name><surname>Erdmann</surname><given-names>E</given-names></name><name><surname>Lohse</surname><given-names>MJ</given-names></name></person-group><article-title>Expression of beta-arrestins and beta-adrenergic receptor kinases in the failing human heart</article-title><source>Circ Res</source><year>1994</year><volume>74</volume><issue>2</issue><fpage>206</fpage><lpage>213</lpage><pub-id pub-id-type="pmid">8293560</pub-id></mixed-citation></ref><ref id="CR35"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Velden</surname><given-names>J</given-names></name><name><surname>Papp</surname><given-names>Z</given-names></name><name><surname>Zaremba</surname><given-names>R</given-names></name><name><surname>Boontje</surname><given-names>NM</given-names></name><name><surname>Jong</surname><given-names>JW</given-names></name><name><surname>Owen</surname><given-names>VJ</given-names></name><name><surname>Burton</surname><given-names>PB</given-names></name><name><surname>Goldmann</surname><given-names>P</given-names></name><name><surname>Jaquet</surname><given-names>K</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name></person-group><article-title>Increased Ca<sup>2+</sup>-sensitivity of the contractile apparatus in end-stage human heart failure results from altered phosphorylation of contractile proteins</article-title><source>Cardiovasc Res</source><year>2003</year><volume>57</volume><issue>1</issue><fpage>37</fpage><lpage>47</lpage><pub-id pub-id-type="doi">10.1016/S0008-6363(02)00606-5</pub-id><pub-id pub-id-type="pmid">12504812</pub-id></mixed-citation></ref><ref id="CR36"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Heerebeek</surname><given-names>L</given-names></name><name><surname>Borbély</surname><given-names>A</given-names></name><name><surname>Niessen</surname><given-names>HW</given-names></name><name><surname>Bronzwaer</surname><given-names>JG</given-names></name><name><surname>Velden</surname><given-names>J</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name><name><surname>Linke</surname><given-names>WA</given-names></name><name><surname>Laarman</surname><given-names>GJ</given-names></name><name><surname>Paulus</surname><given-names>WJ</given-names></name></person-group><article-title>Myocardial structure and function differ in systolic and diastolic heart failure</article-title><source>Circulation</source><year>2006</year><volume>113</volume><issue>16</issue><fpage>1966</fpage><lpage>1973</lpage><pub-id pub-id-type="doi">10.1161/CIRCULATIONAHA.105.587519</pub-id><pub-id pub-id-type="pmid">16618817</pub-id></mixed-citation></ref><ref id="CR37"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Vinge</surname><given-names>LE</given-names></name><name><surname>Øie</surname><given-names>E</given-names></name><name><surname>Andersson</surname><given-names>Y</given-names></name><name><surname>Grøgaard</surname><given-names>HK</given-names></name><name><surname>Andersen</surname><given-names>G</given-names></name><name><surname>Attramadal</surname><given-names>H</given-names></name></person-group><article-title>Myocardial distribution and regulation of GRK and beta-arrestin isoforms in congestive heart failure in rats</article-title><source>Am J Physiol Heart Circ Physiol</source><year>2001</year><volume>281</volume><issue>6</issue><fpage>H2490</fpage><lpage>H2499</lpage><pub-id pub-id-type="pmid">11709416</pub-id></mixed-citation></ref><ref id="CR38"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wang</surname><given-names>X</given-names></name><name><surname>Dhalla</surname><given-names>NS</given-names></name></person-group><article-title>Modifications of β-adrenoceptor signal transduction pathway by genetic manipulation and heart failure</article-title><source>Mol Cell Biochem</source><year>2000</year><volume>214</volume><issue>1–2</issue><fpage>131</fpage><lpage>155</lpage><pub-id pub-id-type="doi">10.1023/A:1007131925048</pub-id><pub-id pub-id-type="pmid">11195784</pub-id></mixed-citation></ref><ref id="CR39"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Weber</surname><given-names>KT</given-names></name></person-group><article-title>Cardiac interstitium in health and disease: the fibrillar collagen network</article-title><source>J Am Coll Cardiol</source><year>1989</year><volume>13</volume><issue>7</issue><fpage>1637</fpage><lpage>1652</lpage><pub-id pub-id-type="doi">10.1016/0735-1097(89)90360-4</pub-id><pub-id pub-id-type="pmid">2656824</pub-id></mixed-citation></ref><ref id="CR40"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wolff</surname><given-names>MR</given-names></name><name><surname>Buck</surname><given-names>SH</given-names></name><name><surname>Stoker</surname><given-names>SW</given-names></name><name><surname>Greaser</surname><given-names>ML</given-names></name><name><surname>Mentzer</surname><given-names>RM</given-names></name></person-group><article-title>Myofibrillar calcium sensitivity of isometric tension is increased in human dilated cardiomyopathies: role of altered beta-adrenergically mediated protein phosphorylation</article-title><source>J Clin Invest</source><year>1996</year><volume>98</volume><issue>1</issue><fpage>167</fpage><lpage>176</lpage><pub-id pub-id-type="doi">10.1172/JCI118762</pub-id><pub-id pub-id-type="pmid">8690789</pub-id></mixed-citation></ref><ref id="CR41"><mixed-citation publication-type="journal"><person-group person-group-type="author"><collab>World Medical Association Declaration of Helsinki</collab></person-group><article-title>Recommendations guiding physicians in biomedical research involving human subjects</article-title><source>Cardiovasc Res</source><year>1997</year><volume>35</volume><fpage>2</fpage><lpage>3</lpage><pub-id pub-id-type="doi">10.1016/S0008-6363(97)00109-0</pub-id><pub-id pub-id-type="pmid">9302340</pub-id></mixed-citation></ref><ref id="CR42"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zaremba</surname><given-names>R</given-names></name><name><surname>Merkus</surname><given-names>D</given-names></name><name><surname>Hamdani</surname><given-names>N</given-names></name><name><surname>Lamers</surname><given-names>JMJ</given-names></name><name><surname>Paulus</surname><given-names>WJ</given-names></name><name><surname>Remedios</surname><given-names>C</given-names></name><name><surname>Duncker</surname><given-names>DJ</given-names></name><name><surname>Stienen</surname><given-names>GJM</given-names></name><name><surname>Velden</surname><given-names>J</given-names></name></person-group><article-title>Quantitative analysis of myofilament protein phosphorylation in small cardiac biopsies</article-title><source>Proteomics Clin Appl</source><year>2007</year><volume>1</volume><fpage>1285</fpage><lpage>1290</lpage><pub-id pub-id-type="doi">10.1002/prca.200600891</pub-id><pub-id pub-id-type="pmid">21136625</pub-id></mixed-citation></ref><ref id="CR43"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname><given-names>R</given-names></name><name><surname>Zhao</surname><given-names>J</given-names></name><name><surname>Mandveno</surname><given-names>A</given-names></name><name><surname>Potter</surname><given-names>JD</given-names></name></person-group><article-title>Cardiac troponin I phosphorylation increases the rate of cardiac muscle relaxation</article-title><source>Circ Res</source><year>1995</year><volume>76</volume><issue>6</issue><fpage>1028</fpage><lpage>1035</lpage><pub-id pub-id-type="pmid">7758157</pub-id></mixed-citation></ref></ref-list></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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