Converging and Unique Mechanisms of Mechanotransduction at Adhesion Sites
The molecular mechanisms by which physical forces control tissue development are beginning to be elucidated. Sites of adhesion between both cells and the extracellular environment [extracellular matrix (ECM) or neighboring cells] contain protein complexes capable of sensing fluctuations in tensile f...
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Veröffentlicht in: | Trends in cell biology 2016-08, Vol.26 (8), p.612-623 |
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description | The molecular mechanisms by which physical forces control tissue development are beginning to be elucidated. Sites of adhesion between both cells and the extracellular environment [extracellular matrix (ECM) or neighboring cells] contain protein complexes capable of sensing fluctuations in tensile forces. Tension-dependent changes in the dynamics and composition of these complexes mark the transformation of physical input into biochemical signals that defines mechanotransduction. It is becoming apparent that, although the core constituents of these different adhesions are distinct, principles and proteins involved in mechanotransduction are conserved. Here, we discuss the current knowledge of overlapping and distinct aspects of mechanotransduction between integrin and cadherin adhesion complexes. |
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Sites of adhesion between both cells and the extracellular environment [extracellular matrix (ECM) or neighboring cells] contain protein complexes capable of sensing fluctuations in tensile forces. Tension-dependent changes in the dynamics and composition of these complexes mark the transformation of physical input into biochemical signals that defines mechanotransduction. It is becoming apparent that, although the core constituents of these different adhesions are distinct, principles and proteins involved in mechanotransduction are conserved. Here, we discuss the current knowledge of overlapping and distinct aspects of mechanotransduction between integrin and cadherin adhesion complexes.</description><identifier>ISSN: 0962-8924</identifier><identifier>EISSN: 1879-3088</identifier><identifier>DOI: 10.1016/j.tcb.2016.03.005</identifier><identifier>PMID: 27036655</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>adhesion ; adhesome ; Animals ; cadherin ; Cadherins - metabolism ; Cell Adhesion ; Focal Adhesions - metabolism ; Humans ; integrin ; Integrins - metabolism ; mechanotransduction ; Mechanotransduction, Cellular ; Models, Biological ; Pathology ; vinculin</subject><ispartof>Trends in cell biology, 2016-08, Vol.26 (8), p.612-623</ispartof><rights>Elsevier Ltd</rights><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. 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Here, we discuss the current knowledge of overlapping and distinct aspects of mechanotransduction between integrin and cadherin adhesion complexes.</description><subject>adhesion</subject><subject>adhesome</subject><subject>Animals</subject><subject>cadherin</subject><subject>Cadherins - metabolism</subject><subject>Cell Adhesion</subject><subject>Focal Adhesions - metabolism</subject><subject>Humans</subject><subject>integrin</subject><subject>Integrins - metabolism</subject><subject>mechanotransduction</subject><subject>Mechanotransduction, Cellular</subject><subject>Models, Biological</subject><subject>Pathology</subject><subject>vinculin</subject><issn>0962-8924</issn><issn>1879-3088</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFv1DAQhS1ERZfCD-CCcuSSMLbj2BESUrUqUKmoh7Zny7EnrZesXeykUv99He3CgQMnz0jvPY2_R8gHCg0F2n3eNbMdGlbGBngDIF6RDVWyrzko9ZpsoO9YrXrWnpK3Oe8AQDLK35BTJoF3nRAbcrmN4QnTvQ_3lQmuugv-94LVT7QPJvi8z1Ucj1uckwnZLXb2MVRmrs7dA-Z1vvEz5nfkZDRTxvfH94zcfbu43f6or66_X27Pr2rbgppr2hoqOPSMGwZq7EbHkDHVWWN6akCg7DgfhBGSDz1IlE4w4UYnhrLScvcZ-XTIfUyxnJpnvffZ4jSZgHHJmiqQoFom-yKlB6lNMeeEo35Mfm_Ss6agV4J6pwtBvRLUwHUhWDwfj_HLsEf31_EHWRF8OQiwfPLJY9LZegwWnU9oZ-2i_2_813_cdvLBWzP9wmfMu7ikUOhpqjPToG_WCtcGaVfaa1vKXwBz1JTk</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Han, Mitchell K.L</creator><creator>de Rooij, Johan</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160801</creationdate><title>Converging and Unique Mechanisms of Mechanotransduction at Adhesion Sites</title><author>Han, Mitchell K.L ; de Rooij, Johan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-14a1530923a208f6fd2e2286caa91a05e7633b5a573b907e7d525dfd5bb901703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>adhesion</topic><topic>adhesome</topic><topic>Animals</topic><topic>cadherin</topic><topic>Cadherins - metabolism</topic><topic>Cell Adhesion</topic><topic>Focal Adhesions - metabolism</topic><topic>Humans</topic><topic>integrin</topic><topic>Integrins - metabolism</topic><topic>mechanotransduction</topic><topic>Mechanotransduction, Cellular</topic><topic>Models, Biological</topic><topic>Pathology</topic><topic>vinculin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Mitchell K.L</creatorcontrib><creatorcontrib>de Rooij, Johan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Trends in cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Mitchell K.L</au><au>de Rooij, Johan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Converging and Unique Mechanisms of Mechanotransduction at Adhesion Sites</atitle><jtitle>Trends in cell biology</jtitle><addtitle>Trends Cell Biol</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>26</volume><issue>8</issue><spage>612</spage><epage>623</epage><pages>612-623</pages><issn>0962-8924</issn><eissn>1879-3088</eissn><abstract>The molecular mechanisms by which physical forces control tissue development are beginning to be elucidated. Sites of adhesion between both cells and the extracellular environment [extracellular matrix (ECM) or neighboring cells] contain protein complexes capable of sensing fluctuations in tensile forces. Tension-dependent changes in the dynamics and composition of these complexes mark the transformation of physical input into biochemical signals that defines mechanotransduction. It is becoming apparent that, although the core constituents of these different adhesions are distinct, principles and proteins involved in mechanotransduction are conserved. Here, we discuss the current knowledge of overlapping and distinct aspects of mechanotransduction between integrin and cadherin adhesion complexes.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27036655</pmid><doi>10.1016/j.tcb.2016.03.005</doi><tpages>12</tpages></addata></record> |
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subjects | adhesion adhesome Animals cadherin Cadherins - metabolism Cell Adhesion Focal Adhesions - metabolism Humans integrin Integrins - metabolism mechanotransduction Mechanotransduction, Cellular Models, Biological Pathology vinculin |
title | Converging and Unique Mechanisms of Mechanotransduction at Adhesion Sites |
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