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Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
Although Snail is essential for disassembly of adherens junctions during epithelial–mesenchymal transitions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the early expression of Snail in that primordium. By combining live im...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738385/ https://www.ncbi.nlm.nih.gov/pubmed/26754645 http://dx.doi.org/10.1083/jcb.201508056 |
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author | Weng, Mo Wieschaus, Eric |
author_facet | Weng, Mo Wieschaus, Eric |
author_sort | Weng, Mo |
collection | PubMed |
description | Although Snail is essential for disassembly of adherens junctions during epithelial–mesenchymal transitions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the early expression of Snail in that primordium. By combining live imaging and quantitative image analysis, we track the behavior of E-cadherin–rich junction clusters, demonstrating that in the early stages of gastrulation most subapical clusters in mesoderm not only persist, but move apically and enhance in density and total intensity. All three phenomena depend on myosin II and are temporally correlated with the pulses of actomyosin accumulation that drive initial cell shape changes during gastrulation. When contractile myosin is absent, the normal Snail expression in mesoderm, or ectopic Snail expression in ectoderm, is sufficient to drive early disassembly of junctions. In both cases, junctional disassembly can be blocked by simultaneous induction of myosin contractility. Our findings provide in vivo evidence for mechanosensitivity of cell–cell junctions and imply that myosin-mediated tension can prevent Snail-driven EMT. |
format | Online Article Text |
id | pubmed-4738385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47383852016-07-18 Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly Weng, Mo Wieschaus, Eric J Cell Biol Research Articles Although Snail is essential for disassembly of adherens junctions during epithelial–mesenchymal transitions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the early expression of Snail in that primordium. By combining live imaging and quantitative image analysis, we track the behavior of E-cadherin–rich junction clusters, demonstrating that in the early stages of gastrulation most subapical clusters in mesoderm not only persist, but move apically and enhance in density and total intensity. All three phenomena depend on myosin II and are temporally correlated with the pulses of actomyosin accumulation that drive initial cell shape changes during gastrulation. When contractile myosin is absent, the normal Snail expression in mesoderm, or ectopic Snail expression in ectoderm, is sufficient to drive early disassembly of junctions. In both cases, junctional disassembly can be blocked by simultaneous induction of myosin contractility. Our findings provide in vivo evidence for mechanosensitivity of cell–cell junctions and imply that myosin-mediated tension can prevent Snail-driven EMT. The Rockefeller University Press 2016-01-18 /pmc/articles/PMC4738385/ /pubmed/26754645 http://dx.doi.org/10.1083/jcb.201508056 Text en © 2016 Wieschaus and Weng 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 Weng, Mo Wieschaus, Eric Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly |
title | Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly |
title_full | Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly |
title_fullStr | Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly |
title_full_unstemmed | Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly |
title_short | Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly |
title_sort | myosin-dependent remodeling of adherens junctions protects junctions from snail-dependent disassembly |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738385/ https://www.ncbi.nlm.nih.gov/pubmed/26754645 http://dx.doi.org/10.1083/jcb.201508056 |
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