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Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres

Cytoskeletal mechanics regulates cell morphodynamics and many physiological processes. While contractility is known to be largely RhoA-dependent, the process by which localized biochemical signals are translated into cell-level responses is poorly understood. Here we combine optogenetic control of R...

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Autores principales: Oakes, Patrick W., Wagner, Elizabeth, Brand, Christoph A., Probst, Dimitri, Linke, Marco, Schwarz, Ulrich S., Glotzer, Michael, Gardel, Margaret L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477492/
https://www.ncbi.nlm.nih.gov/pubmed/28604737
http://dx.doi.org/10.1038/ncomms15817
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author Oakes, Patrick W.
Wagner, Elizabeth
Brand, Christoph A.
Probst, Dimitri
Linke, Marco
Schwarz, Ulrich S.
Glotzer, Michael
Gardel, Margaret L.
author_facet Oakes, Patrick W.
Wagner, Elizabeth
Brand, Christoph A.
Probst, Dimitri
Linke, Marco
Schwarz, Ulrich S.
Glotzer, Michael
Gardel, Margaret L.
author_sort Oakes, Patrick W.
collection PubMed
description Cytoskeletal mechanics regulates cell morphodynamics and many physiological processes. While contractility is known to be largely RhoA-dependent, the process by which localized biochemical signals are translated into cell-level responses is poorly understood. Here we combine optogenetic control of RhoA, live-cell imaging and traction force microscopy to investigate the dynamics of actomyosin-based force generation. Local activation of RhoA not only stimulates local recruitment of actin and myosin but also increased traction forces that rapidly propagate across the cell via stress fibres and drive increased actin flow. Surprisingly, this flow reverses direction when local RhoA activation stops. We identify zyxin as a regulator of stress fibre mechanics, as stress fibres are fluid-like without flow reversal in its absence. Using a physical model, we demonstrate that stress fibres behave elastic-like, even at timescales exceeding turnover of constituent proteins. Such molecular control of actin mechanics likely plays critical roles in regulating morphodynamic events.
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spelling pubmed-54774922017-07-03 Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres Oakes, Patrick W. Wagner, Elizabeth Brand, Christoph A. Probst, Dimitri Linke, Marco Schwarz, Ulrich S. Glotzer, Michael Gardel, Margaret L. Nat Commun Article Cytoskeletal mechanics regulates cell morphodynamics and many physiological processes. While contractility is known to be largely RhoA-dependent, the process by which localized biochemical signals are translated into cell-level responses is poorly understood. Here we combine optogenetic control of RhoA, live-cell imaging and traction force microscopy to investigate the dynamics of actomyosin-based force generation. Local activation of RhoA not only stimulates local recruitment of actin and myosin but also increased traction forces that rapidly propagate across the cell via stress fibres and drive increased actin flow. Surprisingly, this flow reverses direction when local RhoA activation stops. We identify zyxin as a regulator of stress fibre mechanics, as stress fibres are fluid-like without flow reversal in its absence. Using a physical model, we demonstrate that stress fibres behave elastic-like, even at timescales exceeding turnover of constituent proteins. Such molecular control of actin mechanics likely plays critical roles in regulating morphodynamic events. Nature Publishing Group 2017-06-12 /pmc/articles/PMC5477492/ /pubmed/28604737 http://dx.doi.org/10.1038/ncomms15817 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ 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
Oakes, Patrick W.
Wagner, Elizabeth
Brand, Christoph A.
Probst, Dimitri
Linke, Marco
Schwarz, Ulrich S.
Glotzer, Michael
Gardel, Margaret L.
Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres
title Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres
title_full Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres
title_fullStr Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres
title_full_unstemmed Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres
title_short Optogenetic control of RhoA reveals zyxin-mediated elasticity of stress fibres
title_sort optogenetic control of rhoa reveals zyxin-mediated elasticity of stress fibres
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477492/
https://www.ncbi.nlm.nih.gov/pubmed/28604737
http://dx.doi.org/10.1038/ncomms15817
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