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An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity
Epithelia are continuously self-renewed, but how epithelial integrity is maintained during the morphological changes that cells undergo in mitosis is not well understood. Here, we show that as epithelial cells round up when they enter mitosis, they exert tensile forces on neighboring cells. We find...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953256/ https://www.ncbi.nlm.nih.gov/pubmed/33688935 http://dx.doi.org/10.1083/jcb.202001042 |
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author | Monster, Jooske L. Donker, Lisa Vliem, Marjolein J. Win, Zaw Matthews, Helen K. Cheah, Joleen S. Yamada, Soichiro de Rooij, Johan Baum, Buzz Gloerich, Martijn |
author_facet | Monster, Jooske L. Donker, Lisa Vliem, Marjolein J. Win, Zaw Matthews, Helen K. Cheah, Joleen S. Yamada, Soichiro de Rooij, Johan Baum, Buzz Gloerich, Martijn |
author_sort | Monster, Jooske L. |
collection | PubMed |
description | Epithelia are continuously self-renewed, but how epithelial integrity is maintained during the morphological changes that cells undergo in mitosis is not well understood. Here, we show that as epithelial cells round up when they enter mitosis, they exert tensile forces on neighboring cells. We find that mitotic cell–cell junctions withstand these tensile forces through the mechanosensitive recruitment of the actin-binding protein vinculin to cadherin-based adhesions. Surprisingly, vinculin that is recruited to mitotic junctions originates selectively from the neighbors of mitotic cells, resulting in an asymmetric composition of cadherin junctions. Inhibition of junctional vinculin recruitment in neighbors of mitotic cells results in junctional breakage and weakened epithelial barrier. Conversely, the absence of vinculin from the cadherin complex in mitotic cells is necessary to successfully undergo mitotic rounding. Our data thus identify an asymmetric mechanoresponse at cadherin adhesions during mitosis, which is essential to maintain epithelial integrity while at the same time enable the shape changes of mitotic cells. |
format | Online Article Text |
id | pubmed-7953256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79532562021-11-03 An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity Monster, Jooske L. Donker, Lisa Vliem, Marjolein J. Win, Zaw Matthews, Helen K. Cheah, Joleen S. Yamada, Soichiro de Rooij, Johan Baum, Buzz Gloerich, Martijn J Cell Biol Article Epithelia are continuously self-renewed, but how epithelial integrity is maintained during the morphological changes that cells undergo in mitosis is not well understood. Here, we show that as epithelial cells round up when they enter mitosis, they exert tensile forces on neighboring cells. We find that mitotic cell–cell junctions withstand these tensile forces through the mechanosensitive recruitment of the actin-binding protein vinculin to cadherin-based adhesions. Surprisingly, vinculin that is recruited to mitotic junctions originates selectively from the neighbors of mitotic cells, resulting in an asymmetric composition of cadherin junctions. Inhibition of junctional vinculin recruitment in neighbors of mitotic cells results in junctional breakage and weakened epithelial barrier. Conversely, the absence of vinculin from the cadherin complex in mitotic cells is necessary to successfully undergo mitotic rounding. Our data thus identify an asymmetric mechanoresponse at cadherin adhesions during mitosis, which is essential to maintain epithelial integrity while at the same time enable the shape changes of mitotic cells. Rockefeller University Press 2021-03-10 /pmc/articles/PMC7953256/ /pubmed/33688935 http://dx.doi.org/10.1083/jcb.202001042 Text en © 2021 Monster et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/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 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Monster, Jooske L. Donker, Lisa Vliem, Marjolein J. Win, Zaw Matthews, Helen K. Cheah, Joleen S. Yamada, Soichiro de Rooij, Johan Baum, Buzz Gloerich, Martijn An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
title | An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
title_full | An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
title_fullStr | An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
title_full_unstemmed | An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
title_short | An asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
title_sort | asymmetric junctional mechanoresponse coordinates mitotic rounding with epithelial integrity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953256/ https://www.ncbi.nlm.nih.gov/pubmed/33688935 http://dx.doi.org/10.1083/jcb.202001042 |
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