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Myosin II isoforms play distinct roles in adherens junction biogenesis
Adherens junction (AJ) assembly under force is essential for many biological processes like epithelial monolayer bending, collective cell migration, cell extrusion and wound healing. The acto-myosin cytoskeleton acts as a major force-generator during the de novo formation and remodeling of AJ. Here,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756789/ https://www.ncbi.nlm.nih.gov/pubmed/31486768 http://dx.doi.org/10.7554/eLife.46599 |
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author | Heuzé, Mélina L Sankara Narayana, Gautham Hari Narayana D'Alessandro, Joseph Cellerin, Victor Dang, Tien Williams, David S Van Hest, Jan CM Marcq, Philippe Mège, René-Marc Ladoux, Benoit |
author_facet | Heuzé, Mélina L Sankara Narayana, Gautham Hari Narayana D'Alessandro, Joseph Cellerin, Victor Dang, Tien Williams, David S Van Hest, Jan CM Marcq, Philippe Mège, René-Marc Ladoux, Benoit |
author_sort | Heuzé, Mélina L |
collection | PubMed |
description | Adherens junction (AJ) assembly under force is essential for many biological processes like epithelial monolayer bending, collective cell migration, cell extrusion and wound healing. The acto-myosin cytoskeleton acts as a major force-generator during the de novo formation and remodeling of AJ. Here, we investigated the role of non-muscle myosin II isoforms (NMIIA and NMIIB) in epithelial junction assembly. NMIIA and NMIIB differentially regulate biogenesis of AJ through association with distinct actin networks. Analysis of junction dynamics, actin organization, and mechanical forces of control and knockdown cells for myosins revealed that NMIIA provides the mechanical tugging force necessary for cell-cell junction reinforcement and maintenance. NMIIB is involved in E-cadherin clustering, maintenance of a branched actin layer connecting E-cadherin complexes and perijunctional actin fibres leading to the building-up of anisotropic stress. These data reveal unanticipated complementary functions of NMIIA and NMIIB in the biogenesis and integrity of AJ. |
format | Online Article Text |
id | pubmed-6756789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67567892019-09-25 Myosin II isoforms play distinct roles in adherens junction biogenesis Heuzé, Mélina L Sankara Narayana, Gautham Hari Narayana D'Alessandro, Joseph Cellerin, Victor Dang, Tien Williams, David S Van Hest, Jan CM Marcq, Philippe Mège, René-Marc Ladoux, Benoit eLife Cell Biology Adherens junction (AJ) assembly under force is essential for many biological processes like epithelial monolayer bending, collective cell migration, cell extrusion and wound healing. The acto-myosin cytoskeleton acts as a major force-generator during the de novo formation and remodeling of AJ. Here, we investigated the role of non-muscle myosin II isoforms (NMIIA and NMIIB) in epithelial junction assembly. NMIIA and NMIIB differentially regulate biogenesis of AJ through association with distinct actin networks. Analysis of junction dynamics, actin organization, and mechanical forces of control and knockdown cells for myosins revealed that NMIIA provides the mechanical tugging force necessary for cell-cell junction reinforcement and maintenance. NMIIB is involved in E-cadherin clustering, maintenance of a branched actin layer connecting E-cadherin complexes and perijunctional actin fibres leading to the building-up of anisotropic stress. These data reveal unanticipated complementary functions of NMIIA and NMIIB in the biogenesis and integrity of AJ. eLife Sciences Publications, Ltd 2019-09-05 /pmc/articles/PMC6756789/ /pubmed/31486768 http://dx.doi.org/10.7554/eLife.46599 Text en © 2019, Heuzé et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Heuzé, Mélina L Sankara Narayana, Gautham Hari Narayana D'Alessandro, Joseph Cellerin, Victor Dang, Tien Williams, David S Van Hest, Jan CM Marcq, Philippe Mège, René-Marc Ladoux, Benoit Myosin II isoforms play distinct roles in adherens junction biogenesis |
title | Myosin II isoforms play distinct roles in adherens junction biogenesis |
title_full | Myosin II isoforms play distinct roles in adherens junction biogenesis |
title_fullStr | Myosin II isoforms play distinct roles in adherens junction biogenesis |
title_full_unstemmed | Myosin II isoforms play distinct roles in adherens junction biogenesis |
title_short | Myosin II isoforms play distinct roles in adherens junction biogenesis |
title_sort | myosin ii isoforms play distinct roles in adherens junction biogenesis |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756789/ https://www.ncbi.nlm.nih.gov/pubmed/31486768 http://dx.doi.org/10.7554/eLife.46599 |
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