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Membrane-anchored Serine Protease Matriptase Is a Trigger of Pulmonary Fibrogenesis.

Identifieur interne : 002056 ( PubMed/Curation ); précédent : 002055; suivant : 002057

Membrane-anchored Serine Protease Matriptase Is a Trigger of Pulmonary Fibrogenesis.

Auteurs : Olivier Bardou [France] ; Awen Menou [France] ; Charlène François [France] ; Jan Willem Duitman [Pays-Bas] ; Jan H. Von Der Thüsen [Pays-Bas] ; Raphaël Borie [France] ; Katiuchia Uzzun Sales [États-Unis] ; Kathrin Mutze [Allemagne] ; Yves Castier [France] ; Edouard Sage ; Ligong Liu [Australie] ; Thomas H. Bugge [États-Unis] ; David P. Fairlie [Australie] ; Mélanie Königshoff [Allemagne] ; Bruno Crestani [France] ; Keren S. Borensztajn [France]

Source :

RBID : pubmed:26599507

Descripteurs français

English descriptors

Abstract

Idiopathic pulmonary fibrosis (IPF) is a devastating disease that remains refractory to current therapies.

DOI: 10.1164/rccm.201502-0299OC
PubMed: 26599507

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pubmed:26599507

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Edouard Sage
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</affiliation>

Le document en format XML

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<term>Humans</term>
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<term>Lung (metabolism)</term>
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<term>Adulte d'âge moyen</term>
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<term>Modèles animaux de maladie humaine</term>
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<div type="abstract" xml:lang="en">Idiopathic pulmonary fibrosis (IPF) is a devastating disease that remains refractory to current therapies.</div>
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</JournalIssue>
<Title>American journal of respiratory and critical care medicine</Title>
<ISOAbbreviation>Am. J. Respir. Crit. Care Med.</ISOAbbreviation>
</Journal>
<ArticleTitle>Membrane-anchored Serine Protease Matriptase Is a Trigger of Pulmonary Fibrogenesis.</ArticleTitle>
<Pagination>
<MedlinePgn>847-60</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1164/rccm.201502-0299OC</ELocationID>
<Abstract>
<AbstractText Label="RATIONALE" NlmCategory="BACKGROUND">Idiopathic pulmonary fibrosis (IPF) is a devastating disease that remains refractory to current therapies.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To characterize the expression and activity of the membrane-anchored serine protease matriptase in IPF in humans and unravel its potential role in human and experimental pulmonary fibrogenesis.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Matriptase expression was assessed in tissue specimens from patients with IPF versus control subjects using quantitative reverse transcriptase-polymerase chain reaction, immunohistochemistry, and Western blotting, while matriptase activity was monitored by fluorogenic substrate cleavage. Matriptase-induced fibroproliferative responses and the receptor involved were characterized in human primary pulmonary fibroblasts by Western blot, viability, and migration assays. In the murine model of bleomycin-induced pulmonary fibrosis, the consequences of matriptase depletion, either by using the pharmacological inhibitor camostat mesilate (CM), or by genetic down-regulation using matriptase hypomorphic mice, were characterized by quantification of secreted collagen and immunostainings.</AbstractText>
<AbstractText Label="MEASUREMENTS AND MAIN RESULTS" NlmCategory="RESULTS">Matriptase expression and activity were up-regulated in IPF and bleomycin-induced pulmonary fibrosis. In cultured human pulmonary fibroblasts, matriptase expression was significantly induced by transforming growth factor-β. Furthermore, matriptase elicited signaling via protease-activated receptor-2 (PAR-2), and promoted fibroblast activation, proliferation, and migration. In the experimental bleomycin model, matriptase depletion, by the pharmacological inhibitor CM or by genetic down-regulation, diminished lung injury, collagen production, and transforming growth factor-β expression and signaling.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">These results implicate increased matriptase expression and activity in the pathogenesis of pulmonary fibrosis in human IPF and in an experimental mouse model. Overall, targeting matriptase, or treatment by CM, which is already in clinical use for other diseases, may represent potential therapies for IPF.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Bardou</LastName>
<ForeName>Olivier</ForeName>
<Initials>O</Initials>
<AffiliationInfo>
<Affiliation>1 Inserm UMR1152, Medical School Xavier Bichat, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>2 Université Paris Diderot, Sorbonne Paris Cité, Département Hospitalo-universitaire FIRE (Fibrosis, Inflammation and Remodeling) and LabEx Inflamex, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Menou</LastName>
<ForeName>Awen</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>1 Inserm UMR1152, Medical School Xavier Bichat, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>2 Université Paris Diderot, Sorbonne Paris Cité, Département Hospitalo-universitaire FIRE (Fibrosis, Inflammation and Remodeling) and LabEx Inflamex, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>François</LastName>
<ForeName>Charlène</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>1 Inserm UMR1152, Medical School Xavier Bichat, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>2 Université Paris Diderot, Sorbonne Paris Cité, Département Hospitalo-universitaire FIRE (Fibrosis, Inflammation and Remodeling) and LabEx Inflamex, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Duitman</LastName>
<ForeName>Jan Willem</ForeName>
<Initials>JW</Initials>
<AffiliationInfo>
<Affiliation>3 Center for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, the Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>von der Thüsen</LastName>
<ForeName>Jan H</ForeName>
<Initials>JH</Initials>
<AffiliationInfo>
<Affiliation>4 Department of Pathology, Erasmus Medical Centre, Rotterdam, the Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Borie</LastName>
<ForeName>Raphaël</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>2 Université Paris Diderot, Sorbonne Paris Cité, Département Hospitalo-universitaire FIRE (Fibrosis, Inflammation and Remodeling) and LabEx Inflamex, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>5 Assistance Publique-Hôpitaux de Paris, Department of Pulmonology A, Competence Center for Rare Lung Diseases, Bichat-Claude Bernard University Hospital, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sales</LastName>
<ForeName>Katiuchia Uzzun</ForeName>
<Initials>KU</Initials>
<AffiliationInfo>
<Affiliation>6 Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>7 Department of Cell and Molecular Biology, Ribeirão Preto School of Medicine, University of São Paulo Ribeirão Preto, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mutze</LastName>
<ForeName>Kathrin</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>8 Member of the German Center of Lung Research, Comprehensive Pneumology Center, University Hospital, Ludwig-Maximilians University, Helmholtz Zentrum München, Munich, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Castier</LastName>
<ForeName>Yves</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>9 Assistance Publique-Hôpitaux de Paris, Department of Vascular and Thoracic Surgery, Bichat-Claude Bernard University Hospital, Denis Diderot University and Medical School Paris VII, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sage</LastName>
<ForeName>Edouard</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>10 Department of Thoracic Surgery and Lung Transplantation, Hôpital Foch, Suresnes, France; and.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Liu</LastName>
<ForeName>Ligong</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>11 Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bugge</LastName>
<ForeName>Thomas H</ForeName>
<Initials>TH</Initials>
<AffiliationInfo>
<Affiliation>6 Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fairlie</LastName>
<ForeName>David P</ForeName>
<Initials>DP</Initials>
<AffiliationInfo>
<Affiliation>11 Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Königshoff</LastName>
<ForeName>Mélanie</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>8 Member of the German Center of Lung Research, Comprehensive Pneumology Center, University Hospital, Ludwig-Maximilians University, Helmholtz Zentrum München, Munich, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Crestani</LastName>
<ForeName>Bruno</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>1 Inserm UMR1152, Medical School Xavier Bichat, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>2 Université Paris Diderot, Sorbonne Paris Cité, Département Hospitalo-universitaire FIRE (Fibrosis, Inflammation and Remodeling) and LabEx Inflamex, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>5 Assistance Publique-Hôpitaux de Paris, Department of Pulmonology A, Competence Center for Rare Lung Diseases, Bichat-Claude Bernard University Hospital, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Borensztajn</LastName>
<ForeName>Keren S</ForeName>
<Initials>KS</Initials>
<AffiliationInfo>
<Affiliation>1 Inserm UMR1152, Medical School Xavier Bichat, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>2 Université Paris Diderot, Sorbonne Paris Cité, Département Hospitalo-universitaire FIRE (Fibrosis, Inflammation and Remodeling) and LabEx Inflamex, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<Agency>Intramural NIH HHS</Agency>
<Country>United States</Country>
</Grant>
</GrantList>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D052060">Research Support, N.I.H., Intramural</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<Country>United States</Country>
<MedlineTA>Am J Respir Crit Care Med</MedlineTA>
<NlmUniqueID>9421642</NlmUniqueID>
<ISSNLinking>1073-449X</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>EC 3.4.-</RegistryNumber>
<NameOfSubstance UI="D057057">Serine Proteases</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 3.4.21.-</RegistryNumber>
<NameOfSubstance UI="D012697">Serine Endopeptidases</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 3.4.21.-</RegistryNumber>
<NameOfSubstance UI="C485595">matriptase</NameOfSubstance>
</Chemical>
</ChemicalList>
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<CitationSubset>IM</CitationSubset>
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<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015153" MajorTopicYN="N">Blotting, Western</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D004195" MajorTopicYN="N">Disease Models, Animal</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D054990" MajorTopicYN="N">Idiopathic Pulmonary Fibrosis</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
<QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008168" MajorTopicYN="N">Lung</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
<QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008810" MajorTopicYN="N">Mice, Inbred C57BL</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016133" MajorTopicYN="N">Polymerase Chain Reaction</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012697" MajorTopicYN="N">Serine Endopeptidases</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D057057" MajorTopicYN="N">Serine Proteases</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
</MeshHeadingList>
<OtherID Source="NLM">PMC4849177 [Available on 04/15/17]</OtherID>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">camostat mesilate</Keyword>
<Keyword MajorTopicYN="N">fibroblast</Keyword>
<Keyword MajorTopicYN="N">idiopathic pulmonary fibrosis</Keyword>
<Keyword MajorTopicYN="N">matriptase</Keyword>
<Keyword MajorTopicYN="N">protease-activated receptor-2</Keyword>
</KeywordList>
</MedlineCitation>
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<History>
<PubMedPubDate PubStatus="entrez">
<Year>2015</Year>
<Month>11</Month>
<Day>25</Day>
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<Year>2015</Year>
<Month>11</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline">
<Year>2016</Year>
<Month>9</Month>
<Day>1</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
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<ArticleId IdType="pubmed">26599507</ArticleId>
<ArticleId IdType="doi">10.1164/rccm.201502-0299OC</ArticleId>
<ArticleId IdType="pmc">PMC4849177</ArticleId>
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HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Curation/RBID.i   -Sk "pubmed:26599507" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Curation/biblio.hfd   \
       | NlmPubMed2Wicri -a AustralieFrV1 

Wicri

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