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Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling

Tissue remodeling requires cell shape changes associated with pulsation and flow of the actomyosin cytoskeleton. Here we describe the hydrodynamics of actomyosin as a confined active elastomer with turnover of its components. Our treatment is adapted to describe the diversity of contractile dynamica...

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Autores principales: Banerjee, Deb Sankar, Munjal, Akankshi, Lecuit, Thomas, Rao, Madan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783953/
https://www.ncbi.nlm.nih.gov/pubmed/29066711
http://dx.doi.org/10.1038/s41467-017-01130-1
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author Banerjee, Deb Sankar
Munjal, Akankshi
Lecuit, Thomas
Rao, Madan
author_facet Banerjee, Deb Sankar
Munjal, Akankshi
Lecuit, Thomas
Rao, Madan
author_sort Banerjee, Deb Sankar
collection PubMed
description Tissue remodeling requires cell shape changes associated with pulsation and flow of the actomyosin cytoskeleton. Here we describe the hydrodynamics of actomyosin as a confined active elastomer with turnover of its components. Our treatment is adapted to describe the diversity of contractile dynamical regimes observed in vivo. When myosin-induced contractile stresses are low, the deformations of the active elastomer are affine and exhibit spontaneous oscillations, propagating waves, contractile collapse and spatiotemporal chaos. We study the nucleation, growth and coalescence of actomyosin-dense regions that, beyond a threshold, spontaneously move as a spatially localized traveling front. Large myosin-induced contractile stresses lead to nonaffine deformations due to enhanced actin and crosslinker turnover. This results in a transient actin network that is constantly remodeling and naturally accommodates intranetwork flows of the actomyosin-dense regions. We verify many predictions of our study in Drosophila embryonic epithelial cells undergoing neighbor exchange during germband extension.
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spelling pubmed-57839532018-01-26 Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling Banerjee, Deb Sankar Munjal, Akankshi Lecuit, Thomas Rao, Madan Nat Commun Article Tissue remodeling requires cell shape changes associated with pulsation and flow of the actomyosin cytoskeleton. Here we describe the hydrodynamics of actomyosin as a confined active elastomer with turnover of its components. Our treatment is adapted to describe the diversity of contractile dynamical regimes observed in vivo. When myosin-induced contractile stresses are low, the deformations of the active elastomer are affine and exhibit spontaneous oscillations, propagating waves, contractile collapse and spatiotemporal chaos. We study the nucleation, growth and coalescence of actomyosin-dense regions that, beyond a threshold, spontaneously move as a spatially localized traveling front. Large myosin-induced contractile stresses lead to nonaffine deformations due to enhanced actin and crosslinker turnover. This results in a transient actin network that is constantly remodeling and naturally accommodates intranetwork flows of the actomyosin-dense regions. We verify many predictions of our study in Drosophila embryonic epithelial cells undergoing neighbor exchange during germband extension. Nature Publishing Group UK 2017-10-24 /pmc/articles/PMC5783953/ /pubmed/29066711 http://dx.doi.org/10.1038/s41467-017-01130-1 Text en © The Author(s) 2017 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
Banerjee, Deb Sankar
Munjal, Akankshi
Lecuit, Thomas
Rao, Madan
Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
title Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
title_full Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
title_fullStr Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
title_full_unstemmed Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
title_short Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
title_sort actomyosin pulsation and flows in an active elastomer with turnover and network remodeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783953/
https://www.ncbi.nlm.nih.gov/pubmed/29066711
http://dx.doi.org/10.1038/s41467-017-01130-1
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