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MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis

Constriction of the apical plasma membrane is a hallmark of epithelial cells that underlies cell shape changes in tissue morphogenesis and maintenance of tissue integrity in homeostasis. Contractile force is exerted by a cortical actomyosin network that is anchored to the plasma membrane by the apic...

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Autores principales: Matsuzawa, Kenji, Ohga, Hayato, Shigetomi, Kenta, Shiiya, Tomohiro, Hirashima, Masanori, Ikenouchi, Junichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954791/
https://www.ncbi.nlm.nih.gov/pubmed/33712709
http://dx.doi.org/10.1038/s42003-021-01874-z
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author Matsuzawa, Kenji
Ohga, Hayato
Shigetomi, Kenta
Shiiya, Tomohiro
Hirashima, Masanori
Ikenouchi, Junichi
author_facet Matsuzawa, Kenji
Ohga, Hayato
Shigetomi, Kenta
Shiiya, Tomohiro
Hirashima, Masanori
Ikenouchi, Junichi
author_sort Matsuzawa, Kenji
collection PubMed
description Constriction of the apical plasma membrane is a hallmark of epithelial cells that underlies cell shape changes in tissue morphogenesis and maintenance of tissue integrity in homeostasis. Contractile force is exerted by a cortical actomyosin network that is anchored to the plasma membrane by the apical junctional complexes (AJC). In this study, we present evidence that MAGI proteins, structural components of AJC whose function remained unclear, regulate apical constriction of epithelial cells through the Par polarity proteins. We reveal that MAGIs are required to uniformly distribute Partitioning defective-3 (Par-3) at AJC of cells throughout the epithelial monolayer. MAGIs recruit ankyrin-repeat-, SH3-domain- and proline-rich-region-containing protein 2 (ASPP2) to AJC, which modulates Par-3-aPKC to antagonize ROCK-driven contractility. By coupling the adhesion machinery to the polarity proteins to regulate cellular contractility, we propose that MAGIs play essential and central roles in maintaining steady state intercellular tension throughout the epithelial cell sheet.
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spelling pubmed-79547912021-03-28 MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis Matsuzawa, Kenji Ohga, Hayato Shigetomi, Kenta Shiiya, Tomohiro Hirashima, Masanori Ikenouchi, Junichi Commun Biol Article Constriction of the apical plasma membrane is a hallmark of epithelial cells that underlies cell shape changes in tissue morphogenesis and maintenance of tissue integrity in homeostasis. Contractile force is exerted by a cortical actomyosin network that is anchored to the plasma membrane by the apical junctional complexes (AJC). In this study, we present evidence that MAGI proteins, structural components of AJC whose function remained unclear, regulate apical constriction of epithelial cells through the Par polarity proteins. We reveal that MAGIs are required to uniformly distribute Partitioning defective-3 (Par-3) at AJC of cells throughout the epithelial monolayer. MAGIs recruit ankyrin-repeat-, SH3-domain- and proline-rich-region-containing protein 2 (ASPP2) to AJC, which modulates Par-3-aPKC to antagonize ROCK-driven contractility. By coupling the adhesion machinery to the polarity proteins to regulate cellular contractility, we propose that MAGIs play essential and central roles in maintaining steady state intercellular tension throughout the epithelial cell sheet. Nature Publishing Group UK 2021-03-12 /pmc/articles/PMC7954791/ /pubmed/33712709 http://dx.doi.org/10.1038/s42003-021-01874-z Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Matsuzawa, Kenji
Ohga, Hayato
Shigetomi, Kenta
Shiiya, Tomohiro
Hirashima, Masanori
Ikenouchi, Junichi
MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
title MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
title_full MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
title_fullStr MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
title_full_unstemmed MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
title_short MAGIs regulate aPKC to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
title_sort magis regulate apkc to enable balanced distribution of intercellular tension for epithelial sheet homeostasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954791/
https://www.ncbi.nlm.nih.gov/pubmed/33712709
http://dx.doi.org/10.1038/s42003-021-01874-z
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