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Upregulated proteoglycan-related signaling pathways in fluid flow shear stress-treated podocytes.

Identifieur interne : 000011 ( Main/Exploration ); précédent : 000010; suivant : 000012

Upregulated proteoglycan-related signaling pathways in fluid flow shear stress-treated podocytes.

Auteurs : Tarak Srivastava [États-Unis] ; Trupti Joshi [États-Unis] ; Yuexu Jiang [États-Unis] ; Daniel P. Heruth [États-Unis] ; Mohamed H. Rezaiekhaligh [États-Unis] ; Jan Novak [États-Unis] ; Vincent S. Staggs [États-Unis] ; Uri S. Alon [États-Unis] ; Robert E. Garola ; Ashraf El-Meanawy [États-Unis] ; Ellen T. Mccarthy [États-Unis] ; Jianping Zhou [États-Unis] ; Varun C. Boinpelly [États-Unis] ; Ram Sharma [États-Unis] ; Virginia J. Savin [États-Unis] ; Mukut Sharma [États-Unis]

Source :

RBID : pubmed:32628542

Descripteurs français

English descriptors

Abstract

The ultrafiltrate flow over the major processes and cell body generates fluid flow shear stress (FFSS) on podocytes. Hyperfiltration-associated increase in FFSS can lead to podocyte injury and detachment. Previously, we showed that FFSS-induced upregulation of the cyclooxygenase 2 (COX2)-PGE2-prostaglandin E receptor 2 (EP2) axis in podocytes activates Akt-glycogen synthase kinase-3β-β-catenin and MAPK/ERK signaling in response to FFSS. Integrative MultiOmics Pathway Resolution (IMPRes) is a new bioinformatic tool that enables simultaneous time-series analysis of more than two groups to identify pathways and molecular connections. In the present study, we used previously characterized COX2 [prostaglandin-endoperoxide synthase 2 (Ptgs2)], EP2 (Ptger2), and β1-catenin (Ctnnb1) as "seed genes" from an array data set of four groups analyzed over a time course. The 3 seed genes shared 7 pathways and 50 genes of 14 pathways and 89 genes identified by IMPRes. A composite of signaling pathways highlighted the temporal molecular connections during mechanotransduction signaling in FFSS-treated podocytes. We investigated the "proteoglycans in cancer" and "galactose metabolism" pathways predicted by IMPRes. A custom-designed PCR array validated 60.7% of the genes predicted by IMPRes analysis, including genes for the above-named pathways. Further validation using Western blot analysis showed increased expression of phosho-Erbb2, phospho-mammalian target of rapamycin (mTOR), CD44, and hexokinase II (Hk2); decreased total Erbb2, galactose mutarotase (Galm), and β-1,4-galactosyltransferase 1 (B4galt1); and unchanged total mTOR and AKT3. These findings corroborate our previously reported results. This study demonstrates the potential of the IMPRes method to identify novel pathways. Identifying the "proteoglycans in cancer" and "galactose metabolism" pathways has generated a lead to study the significance of FFSS-induced glycocalyx remodeling and possible detachment of podocytes from the glomerular matrix.

DOI: 10.1152/ajprenal.00183.2020
PubMed: 32628542
PubMed Central: PMC7473905


Affiliations:


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Le document en format XML

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<title level="j">American journal of physiology. Renal physiology</title>
<idno type="eISSN">1522-1466</idno>
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<date when="2020" type="published">2020</date>
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<term>Cyclooxygenase 2 (metabolism)</term>
<term>Kidney Glomerulus (metabolism)</term>
<term>Mechanotransduction, Cellular (physiology)</term>
<term>Podocytes (metabolism)</term>
<term>Proteoglycans (metabolism)</term>
<term>Receptors, Prostaglandin E, EP2 Subtype (metabolism)</term>
<term>Stress, Mechanical (MeSH)</term>
<term>TOR Serine-Threonine Kinases (metabolism)</term>
<term>Transcriptional Activation (physiology)</term>
<term>Up-Regulation (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Activation de la transcription (physiologie)</term>
<term>Contrainte mécanique (MeSH)</term>
<term>Cyclooxygenase 2 (métabolisme)</term>
<term>Glomérule rénal (métabolisme)</term>
<term>Mécanotransduction cellulaire (physiologie)</term>
<term>Podocytes (métabolisme)</term>
<term>Protéoglycanes (métabolisme)</term>
<term>Régulation positive (MeSH)</term>
<term>Sous-type EP2 des récepteurs des prostaglandines E (métabolisme)</term>
<term>Sérine-thréonine kinases TOR (métabolisme)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Cyclooxygenase 2</term>
<term>Proteoglycans</term>
<term>Receptors, Prostaglandin E, EP2 Subtype</term>
<term>TOR Serine-Threonine Kinases</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Kidney Glomerulus</term>
<term>Podocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Cyclooxygenase 2</term>
<term>Glomérule rénal</term>
<term>Podocytes</term>
<term>Protéoglycanes</term>
<term>Sous-type EP2 des récepteurs des prostaglandines E</term>
<term>Sérine-thréonine kinases TOR</term>
</keywords>
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<term>Activation de la transcription</term>
<term>Mécanotransduction cellulaire</term>
</keywords>
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<term>Mechanotransduction, Cellular</term>
<term>Transcriptional Activation</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Stress, Mechanical</term>
<term>Up-Regulation</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Contrainte mécanique</term>
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<front>
<div type="abstract" xml:lang="en">The ultrafiltrate flow over the major processes and cell body generates fluid flow shear stress (FFSS) on podocytes. Hyperfiltration-associated increase in FFSS can lead to podocyte injury and detachment. Previously, we showed that FFSS-induced upregulation of the cyclooxygenase 2 (COX2)-PGE
<sub>2</sub>
-prostaglandin E receptor 2 (EP2) axis in podocytes activates Akt-glycogen synthase kinase-3β-β-catenin and MAPK/ERK signaling in response to FFSS. Integrative MultiOmics Pathway Resolution (IMPRes) is a new bioinformatic tool that enables simultaneous time-series analysis of more than two groups to identify pathways and molecular connections. In the present study, we used previously characterized COX2 [prostaglandin-endoperoxide synthase 2 (
<i>Ptgs2</i>
)], EP2 (
<i>Ptger2</i>
), and β1-catenin (
<i>Ctnnb1</i>
) as "seed genes" from an array data set of four groups analyzed over a time course. The 3 seed genes shared 7 pathways and 50 genes of 14 pathways and 89 genes identified by IMPRes. A composite of signaling pathways highlighted the temporal molecular connections during mechanotransduction signaling in FFSS-treated podocytes. We investigated the "proteoglycans in cancer" and "galactose metabolism" pathways predicted by IMPRes. A custom-designed PCR array validated 60.7% of the genes predicted by IMPRes analysis, including genes for the above-named pathways. Further validation using Western blot analysis showed increased expression of phosho-Erbb2, phospho-mammalian target of rapamycin (mTOR), CD44, and hexokinase II (Hk2); decreased total Erbb2, galactose mutarotase (Galm), and β-1,4-galactosyltransferase 1 (B4galt1); and unchanged total mTOR and AKT3. These findings corroborate our previously reported results. This study demonstrates the potential of the IMPRes method to identify novel pathways. Identifying the "proteoglycans in cancer" and "galactose metabolism" pathways has generated a lead to study the significance of FFSS-induced glycocalyx remodeling and possible detachment of podocytes from the glomerular matrix.</div>
</front>
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<Year>2020</Year>
<Month>10</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>10</Month>
<Day>06</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1522-1466</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>319</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2020</Year>
<Month>08</Month>
<Day>01</Day>
</PubDate>
</JournalIssue>
<Title>American journal of physiology. Renal physiology</Title>
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<ArticleTitle>Upregulated proteoglycan-related signaling pathways in fluid flow shear stress-treated podocytes.</ArticleTitle>
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</Pagination>
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<Abstract>
<AbstractText>The ultrafiltrate flow over the major processes and cell body generates fluid flow shear stress (FFSS) on podocytes. Hyperfiltration-associated increase in FFSS can lead to podocyte injury and detachment. Previously, we showed that FFSS-induced upregulation of the cyclooxygenase 2 (COX2)-PGE
<sub>2</sub>
-prostaglandin E receptor 2 (EP2) axis in podocytes activates Akt-glycogen synthase kinase-3β-β-catenin and MAPK/ERK signaling in response to FFSS. Integrative MultiOmics Pathway Resolution (IMPRes) is a new bioinformatic tool that enables simultaneous time-series analysis of more than two groups to identify pathways and molecular connections. In the present study, we used previously characterized COX2 [prostaglandin-endoperoxide synthase 2 (
<i>Ptgs2</i>
)], EP2 (
<i>Ptger2</i>
), and β1-catenin (
<i>Ctnnb1</i>
) as "seed genes" from an array data set of four groups analyzed over a time course. The 3 seed genes shared 7 pathways and 50 genes of 14 pathways and 89 genes identified by IMPRes. A composite of signaling pathways highlighted the temporal molecular connections during mechanotransduction signaling in FFSS-treated podocytes. We investigated the "proteoglycans in cancer" and "galactose metabolism" pathways predicted by IMPRes. A custom-designed PCR array validated 60.7% of the genes predicted by IMPRes analysis, including genes for the above-named pathways. Further validation using Western blot analysis showed increased expression of phosho-Erbb2, phospho-mammalian target of rapamycin (mTOR), CD44, and hexokinase II (Hk2); decreased total Erbb2, galactose mutarotase (Galm), and β-1,4-galactosyltransferase 1 (B4galt1); and unchanged total mTOR and AKT3. These findings corroborate our previously reported results. This study demonstrates the potential of the IMPRes method to identify novel pathways. Identifying the "proteoglycans in cancer" and "galactose metabolism" pathways has generated a lead to study the significance of FFSS-induced glycocalyx remodeling and possible detachment of podocytes from the glomerular matrix.</AbstractText>
</Abstract>
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<LastName>Srivastava</LastName>
<ForeName>Tarak</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Section of Nephrology, Children's Mercy Hospital and University of Missouri, Kansas City, Missouri.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Midwest Veterans' Biomedical Research Foundation, Kansas City, Missouri.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Oral and Craniofacial Sciences, University of Missouri School of Dentistry, Kansas City, Missouri.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Joshi</LastName>
<ForeName>Trupti</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Department of Health Management and Informatics and University of Missouri Informatics Institute, University of Missouri, Columbia, Missouri.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Electrical Engineering and Computer Science, University of Missouri, Columbia, Missouri.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>MU Data Science and Informatics Institute, University of Missouri, Columbia, Missouri.</Affiliation>
</AffiliationInfo>
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<LastName>Jiang</LastName>
<ForeName>Yuexu</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Electrical Engineering and Computer Science, University of Missouri, Columbia, Missouri.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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<ForeName>Mohamed H</ForeName>
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</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
</Author>
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<LastName>Garola</LastName>
<ForeName>Robert E</ForeName>
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</AffiliationInfo>
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<LastName>El-Meanawy</LastName>
<ForeName>Ashraf</ForeName>
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</AffiliationInfo>
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<LastName>Zhou</LastName>
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<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Kansas City Veterans Affairs Medical Center, Kansas City, Missouri.</Affiliation>
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<LastName>Boinpelly</LastName>
<ForeName>Varun C</ForeName>
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<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Kansas City Veterans Affairs Medical Center, Kansas City, Missouri.</Affiliation>
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<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Kansas City Veterans Affairs Medical Center, Kansas City, Missouri.</Affiliation>
</AffiliationInfo>
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<ForeName>Mukut</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas.</Affiliation>
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<AffiliationInfo>
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</AffiliationInfo>
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<Agency>HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)</Agency>
<Country>International</Country>
</Grant>
<Grant>
<GrantID>R01DK064969</GrantID>
<Agency>HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)</Agency>
<Country>International</Country>
</Grant>
<Grant>
<GrantID>BX001037</GrantID>
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<Chemical>
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<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D050199" MajorTopicYN="N">Podocytes</DescriptorName>
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</MeshHeading>
<MeshHeading>
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</MeshHeading>
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<Keyword MajorTopicYN="Y">galactose metabolism</Keyword>
<Keyword MajorTopicYN="Y">glycocalyx</Keyword>
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