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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5783953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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