HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.

Adherens junctions (AJs) are key structures regulating tissue integrity and maintaining adhesion between cells. During morphogenesis, junctional proteins cooperate closely with the actomyosin network to drive cell movement and shape changes. How the junctions integrate the mechanical forces in space...

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Main Authors: Thanh Thi Kim Vuong-Brender, Arthur Boutillon, David Rodriguez, Vincent Lavilley, Michel Labouesse
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5821396?pdf=render
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spelling doaj-0a237717f3c149c7bc0a135717f7e8792020-11-25T00:48:31ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01132e019327910.1371/journal.pone.0193279HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.Thanh Thi Kim Vuong-BrenderArthur BoutillonDavid RodriguezVincent LavilleyMichel LabouesseAdherens junctions (AJs) are key structures regulating tissue integrity and maintaining adhesion between cells. During morphogenesis, junctional proteins cooperate closely with the actomyosin network to drive cell movement and shape changes. How the junctions integrate the mechanical forces in space and in time during an in vivo morphogenetic event is still largely unknown, due to a lack of quantitative data. To address this issue, we inserted a functional Fluorescence Resonance Energy Transfer (FRET)-based force biosensor within HMP-1/α-catenin of Caenorhabditis elegans. We find that the tension exerted on HMP-1 has a cell-specific distribution, is actomyosin-dependent, but is regulated differently from the tension on the actin cortex during embryonic elongation. By using time-lapse analysis of mutants and tissue-specific rescue experiments, we confirm the role of VAB-9/Claudin as an actin bundle anchor. Nevertheless, the tension exerted on HMP-1 did not increase in the absence of VAB-9/Claudin, suggesting that HMP-1 activity is not upregulated to compensate for loss of VAB-9. Our data indicate that HMP-1 does not modulate HMR-1/E-cadherin turnover, is required to recruit junctional actin but not stress fiber-like actin bundles. Altogether, our data suggest that HMP-1/α-catenin acts to promote the mechanical integrity of adherens junctions.http://europepmc.org/articles/PMC5821396?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Thanh Thi Kim Vuong-Brender
Arthur Boutillon
David Rodriguez
Vincent Lavilley
Michel Labouesse
spellingShingle Thanh Thi Kim Vuong-Brender
Arthur Boutillon
David Rodriguez
Vincent Lavilley
Michel Labouesse
HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
PLoS ONE
author_facet Thanh Thi Kim Vuong-Brender
Arthur Boutillon
David Rodriguez
Vincent Lavilley
Michel Labouesse
author_sort Thanh Thi Kim Vuong-Brender
title HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
title_short HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
title_full HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
title_fullStr HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
title_full_unstemmed HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
title_sort hmp-1/α-catenin promotes junctional mechanical integrity during morphogenesis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Adherens junctions (AJs) are key structures regulating tissue integrity and maintaining adhesion between cells. During morphogenesis, junctional proteins cooperate closely with the actomyosin network to drive cell movement and shape changes. How the junctions integrate the mechanical forces in space and in time during an in vivo morphogenetic event is still largely unknown, due to a lack of quantitative data. To address this issue, we inserted a functional Fluorescence Resonance Energy Transfer (FRET)-based force biosensor within HMP-1/α-catenin of Caenorhabditis elegans. We find that the tension exerted on HMP-1 has a cell-specific distribution, is actomyosin-dependent, but is regulated differently from the tension on the actin cortex during embryonic elongation. By using time-lapse analysis of mutants and tissue-specific rescue experiments, we confirm the role of VAB-9/Claudin as an actin bundle anchor. Nevertheless, the tension exerted on HMP-1 did not increase in the absence of VAB-9/Claudin, suggesting that HMP-1 activity is not upregulated to compensate for loss of VAB-9. Our data indicate that HMP-1 does not modulate HMR-1/E-cadherin turnover, is required to recruit junctional actin but not stress fiber-like actin bundles. Altogether, our data suggest that HMP-1/α-catenin acts to promote the mechanical integrity of adherens junctions.
url http://europepmc.org/articles/PMC5821396?pdf=render
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