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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
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.
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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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