E-cadherin junctions as active mechanical integrators in tissue dynamics.
Identifieur interne : 002D65 ( PubMed/Corpus ); précédent : 002D64; suivant : 002D66E-cadherin junctions as active mechanical integrators in tissue dynamics.
Auteurs : Thomas Lecuit ; Alpha S. YapSource :
- Nature cell biology [ 1476-4679 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Actomyosin, Cadherins.
- metabolism : Cytoskeleton, Epithelial Cells, Intercellular Junctions.
- Animals, Biomechanical Phenomena, Cell Adhesion, Cell Communication, Cell Shape, Humans, Mechanotransduction, Cellular, Morphogenesis, Stress, Mechanical.
Abstract
During epithelial morphogenesis, E-cadherin adhesive junctions play an important part in mechanically coupling the contractile cortices of cells together, thereby distributing the stresses that drive cell rearrangements at both local and tissue levels. Here we discuss the concept that cellular contractility and E-cadherin-based adhesion are functionally integrated by biomechanical feedback pathways that operate on molecular, cellular and tissue scales.
DOI: 10.1038/ncb3136
PubMed: 25925582
Links to Exploration step
pubmed:25925582Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">E-cadherin junctions as active mechanical integrators in tissue dynamics.</title><author><name sortKey="Lecuit, Thomas" sort="Lecuit, Thomas" uniqKey="Lecuit T" first="Thomas" last="Lecuit">Thomas Lecuit</name><affiliation><nlm:affiliation>IBDM, Aix-Marseille Université, CNRS, Campus de Luminy case 907, 13009 Marseille, France.</nlm:affiliation></affiliation></author><author><name sortKey="Yap, Alpha S" sort="Yap, Alpha S" uniqKey="Yap A" first="Alpha S" last="Yap">Alpha S. Yap</name><affiliation><nlm:affiliation>Division of Molecular Cell Biology, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Queensland 4072, Australia.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2015">2015</date><idno type="RBID">pubmed:25925582</idno><idno type="pmid">25925582</idno><idno type="doi">10.1038/ncb3136</idno><idno type="wicri:Area/PubMed/Corpus">002D65</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002D65</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">E-cadherin junctions as active mechanical integrators in tissue dynamics.</title><author><name sortKey="Lecuit, Thomas" sort="Lecuit, Thomas" uniqKey="Lecuit T" first="Thomas" last="Lecuit">Thomas Lecuit</name><affiliation><nlm:affiliation>IBDM, Aix-Marseille Université, CNRS, Campus de Luminy case 907, 13009 Marseille, France.</nlm:affiliation></affiliation></author><author><name sortKey="Yap, Alpha S" sort="Yap, Alpha S" uniqKey="Yap A" first="Alpha S" last="Yap">Alpha S. Yap</name><affiliation><nlm:affiliation>Division of Molecular Cell Biology, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Queensland 4072, Australia.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Nature cell biology</title><idno type="eISSN">1476-4679</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Actomyosin (metabolism)</term><term>Animals</term><term>Biomechanical Phenomena</term><term>Cadherins (metabolism)</term><term>Cell Adhesion</term><term>Cell Communication</term><term>Cell Shape</term><term>Cytoskeleton (metabolism)</term><term>Epithelial Cells (metabolism)</term><term>Humans</term><term>Intercellular Junctions (metabolism)</term><term>Mechanotransduction, Cellular</term><term>Morphogenesis</term><term>Stress, Mechanical</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Actomyosin</term><term>Cadherins</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cytoskeleton</term><term>Epithelial Cells</term><term>Intercellular Junctions</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Biomechanical Phenomena</term><term>Cell Adhesion</term><term>Cell Communication</term><term>Cell Shape</term><term>Humans</term><term>Mechanotransduction, Cellular</term><term>Morphogenesis</term><term>Stress, Mechanical</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">During epithelial morphogenesis, E-cadherin adhesive junctions play an important part in mechanically coupling the contractile cortices of cells together, thereby distributing the stresses that drive cell rearrangements at both local and tissue levels. Here we discuss the concept that cellular contractility and E-cadherin-based adhesion are functionally integrated by biomechanical feedback pathways that operate on molecular, cellular and tissue scales.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25925582</PMID><DateCreated><Year>2015</Year><Month>04</Month><Day>30</Day></DateCreated><DateCompleted><Year>2015</Year><Month>07</Month><Day>09</Day></DateCompleted><DateRevised><Year>2017</Year><Month>07</Month><Day>20</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1476-4679</ISSN><JournalIssue CitedMedium="Internet"><Volume>17</Volume><Issue>5</Issue><PubDate><Year>2015</Year><Month>May</Month></PubDate></JournalIssue><Title>Nature cell biology</Title><ISOAbbreviation>Nat. Cell Biol.</ISOAbbreviation></Journal><ArticleTitle>E-cadherin junctions as active mechanical integrators in tissue dynamics.</ArticleTitle><Pagination><MedlinePgn>533-9</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1038/ncb3136</ELocationID><Abstract><AbstractText>During epithelial morphogenesis, E-cadherin adhesive junctions play an important part in mechanically coupling the contractile cortices of cells together, thereby distributing the stresses that drive cell rearrangements at both local and tissue levels. Here we discuss the concept that cellular contractility and E-cadherin-based adhesion are functionally integrated by biomechanical feedback pathways that operate on molecular, cellular and tissue scales.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Lecuit</LastName><ForeName>Thomas</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>IBDM, Aix-Marseille Université, CNRS, Campus de Luminy case 907, 13009 Marseille, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yap</LastName><ForeName>Alpha S</ForeName><Initials>AS</Initials><AffiliationInfo><Affiliation>Division of Molecular Cell Biology, Institute for Molecular Bioscience, The University of Queensland, St. Lucia, Queensland 4072, Australia.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. 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