Cargando…

Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling

During epithelial contraction, cells generate forces to constrict their surface and, concurrently, fine-tune the length of their adherens junctions to ensure force transmission. While many studies have focused on understanding force generation, little is known on how junctional length is controlled....

Descripción completa

Detalles Bibliográficos
Autores principales: Sumi, Angughali, Hayes, Peran, D’Angelo, Arturo, Colombelli, Julien, Salbreux, Guillaume, Dierkes, Kai, Solon, Jérôme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291457/
https://www.ncbi.nlm.nih.gov/pubmed/30458138
http://dx.doi.org/10.1016/j.devcel.2018.10.025
_version_ 1783380249980960768
author Sumi, Angughali
Hayes, Peran
D’Angelo, Arturo
Colombelli, Julien
Salbreux, Guillaume
Dierkes, Kai
Solon, Jérôme
author_facet Sumi, Angughali
Hayes, Peran
D’Angelo, Arturo
Colombelli, Julien
Salbreux, Guillaume
Dierkes, Kai
Solon, Jérôme
author_sort Sumi, Angughali
collection PubMed
description During epithelial contraction, cells generate forces to constrict their surface and, concurrently, fine-tune the length of their adherens junctions to ensure force transmission. While many studies have focused on understanding force generation, little is known on how junctional length is controlled. Here, we show that, during amnioserosa contraction in Drosophila dorsal closure, adherens junctions reduce their length in coordination with the shrinkage of apical cell area, maintaining a nearly constant junctional straightness. We reveal that junctional straightness and integrity depend on the endocytic machinery and on the mechanosensitive activity of the actomyosin cytoskeleton. On one hand, upon junctional stretch and decrease in E-cadherin density, actomyosin relocalizes from the medial area to the junctions, thus maintaining junctional integrity. On the other hand, when junctions have excess material and ruffles, junction removal is enhanced, and high junctional straightness and tension are restored. These two mechanisms control junctional length and integrity during morphogenesis.
format Online
Article
Text
id pubmed-6291457
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-62914572018-12-17 Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling Sumi, Angughali Hayes, Peran D’Angelo, Arturo Colombelli, Julien Salbreux, Guillaume Dierkes, Kai Solon, Jérôme Dev Cell Article During epithelial contraction, cells generate forces to constrict their surface and, concurrently, fine-tune the length of their adherens junctions to ensure force transmission. While many studies have focused on understanding force generation, little is known on how junctional length is controlled. Here, we show that, during amnioserosa contraction in Drosophila dorsal closure, adherens junctions reduce their length in coordination with the shrinkage of apical cell area, maintaining a nearly constant junctional straightness. We reveal that junctional straightness and integrity depend on the endocytic machinery and on the mechanosensitive activity of the actomyosin cytoskeleton. On one hand, upon junctional stretch and decrease in E-cadherin density, actomyosin relocalizes from the medial area to the junctions, thus maintaining junctional integrity. On the other hand, when junctions have excess material and ruffles, junction removal is enhanced, and high junctional straightness and tension are restored. These two mechanisms control junctional length and integrity during morphogenesis. Cell Press 2018-11-19 /pmc/articles/PMC6291457/ /pubmed/30458138 http://dx.doi.org/10.1016/j.devcel.2018.10.025 Text en © 2018 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sumi, Angughali
Hayes, Peran
D’Angelo, Arturo
Colombelli, Julien
Salbreux, Guillaume
Dierkes, Kai
Solon, Jérôme
Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling
title Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling
title_full Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling
title_fullStr Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling
title_full_unstemmed Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling
title_short Adherens Junction Length during Tissue Contraction Is Controlled by the Mechanosensitive Activity of Actomyosin and Junctional Recycling
title_sort adherens junction length during tissue contraction is controlled by the mechanosensitive activity of actomyosin and junctional recycling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291457/
https://www.ncbi.nlm.nih.gov/pubmed/30458138
http://dx.doi.org/10.1016/j.devcel.2018.10.025
work_keys_str_mv AT sumiangughali adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling
AT hayesperan adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling
AT dangeloarturo adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling
AT colombellijulien adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling
AT salbreuxguillaume adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling
AT dierkeskai adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling
AT solonjerome adherensjunctionlengthduringtissuecontractioniscontrolledbythemechanosensitiveactivityofactomyosinandjunctionalrecycling