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The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity
Oligomerization of cadherins could provide the stability to ensure tissue cohesion. Cadherins mediate cell–cell adhesion by forming trans-interactions. They form cis-interactions whose role could be essential to stabilize intercellular junctions by shifting cadherin clusters from a fluid to an order...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508897/ https://www.ncbi.nlm.nih.gov/pubmed/26195669 http://dx.doi.org/10.1083/jcb.201410111 |
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author | Strale, Pierre-Olivier Duchesne, Laurence Peyret, Grégoire Montel, Lorraine Nguyen, Thao Png, Evelyn Tampé, Robert Troyanovsky, Sergey Hénon, Sylvie Ladoux, Benoit Mège, René-Marc |
author_facet | Strale, Pierre-Olivier Duchesne, Laurence Peyret, Grégoire Montel, Lorraine Nguyen, Thao Png, Evelyn Tampé, Robert Troyanovsky, Sergey Hénon, Sylvie Ladoux, Benoit Mège, René-Marc |
author_sort | Strale, Pierre-Olivier |
collection | PubMed |
description | Oligomerization of cadherins could provide the stability to ensure tissue cohesion. Cadherins mediate cell–cell adhesion by forming trans-interactions. They form cis-interactions whose role could be essential to stabilize intercellular junctions by shifting cadherin clusters from a fluid to an ordered phase. However, no evidence has been provided so far for cadherin oligomerization in cellulo and for its impact on cell–cell contact stability. Visualizing single cadherins within cell membrane at a nanometric resolution, we show that E-cadherins arrange in ordered clusters, providing the first demonstration of the existence of oligomeric cadherins at cell–cell contacts. Studying the consequences of the disruption of the cis-interface, we show that it is not essential for adherens junction formation. Its disruption, however, increased the mobility of junctional E-cadherin. This destabilization strongly affected E-cadherin anchoring to actin and cell–cell rearrangement during collective cell migration, indicating that the formation of oligomeric clusters controls the anchoring of cadherin to actin and cell–cell contact fluidity. |
format | Online Article Text |
id | pubmed-4508897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45088972016-01-20 The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity Strale, Pierre-Olivier Duchesne, Laurence Peyret, Grégoire Montel, Lorraine Nguyen, Thao Png, Evelyn Tampé, Robert Troyanovsky, Sergey Hénon, Sylvie Ladoux, Benoit Mège, René-Marc J Cell Biol Research Articles Oligomerization of cadherins could provide the stability to ensure tissue cohesion. Cadherins mediate cell–cell adhesion by forming trans-interactions. They form cis-interactions whose role could be essential to stabilize intercellular junctions by shifting cadherin clusters from a fluid to an ordered phase. However, no evidence has been provided so far for cadherin oligomerization in cellulo and for its impact on cell–cell contact stability. Visualizing single cadherins within cell membrane at a nanometric resolution, we show that E-cadherins arrange in ordered clusters, providing the first demonstration of the existence of oligomeric cadherins at cell–cell contacts. Studying the consequences of the disruption of the cis-interface, we show that it is not essential for adherens junction formation. Its disruption, however, increased the mobility of junctional E-cadherin. This destabilization strongly affected E-cadherin anchoring to actin and cell–cell rearrangement during collective cell migration, indicating that the formation of oligomeric clusters controls the anchoring of cadherin to actin and cell–cell contact fluidity. The Rockefeller University Press 2015-07-20 /pmc/articles/PMC4508897/ /pubmed/26195669 http://dx.doi.org/10.1083/jcb.201410111 Text en © 2015 Strale et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Strale, Pierre-Olivier Duchesne, Laurence Peyret, Grégoire Montel, Lorraine Nguyen, Thao Png, Evelyn Tampé, Robert Troyanovsky, Sergey Hénon, Sylvie Ladoux, Benoit Mège, René-Marc The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
title | The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
title_full | The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
title_fullStr | The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
title_full_unstemmed | The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
title_short | The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
title_sort | formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508897/ https://www.ncbi.nlm.nih.gov/pubmed/26195669 http://dx.doi.org/10.1083/jcb.201410111 |
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