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Boundaries steer the contraction of active gels

Cells set up contractile actin arrays to drive various shape changes and to exert forces to their environment. To understand their assembly process, we present here a reconstituted contractile system, comprising F-actin and myosin II filaments, where we can control the local activation of myosin by...

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Autores principales: Schuppler, Matthias, Keber, Felix C., Kröger, Martin, Bausch, Andreas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067607/
https://www.ncbi.nlm.nih.gov/pubmed/27739426
http://dx.doi.org/10.1038/ncomms13120
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author Schuppler, Matthias
Keber, Felix C.
Kröger, Martin
Bausch, Andreas R.
author_facet Schuppler, Matthias
Keber, Felix C.
Kröger, Martin
Bausch, Andreas R.
author_sort Schuppler, Matthias
collection PubMed
description Cells set up contractile actin arrays to drive various shape changes and to exert forces to their environment. To understand their assembly process, we present here a reconstituted contractile system, comprising F-actin and myosin II filaments, where we can control the local activation of myosin by light. By stimulating different symmetries, we show that the force balancing at the boundaries determine the shape changes as well as the dynamics of the global contraction. Spatially anisotropic attachment of initially isotropic networks leads to a self-organization of highly aligned contractile fibres, being reminiscent of the order formation in muscles or stress fibres. The observed shape changes and dynamics are fully recovered by a minimal physical model.
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spelling pubmed-50676072016-10-24 Boundaries steer the contraction of active gels Schuppler, Matthias Keber, Felix C. Kröger, Martin Bausch, Andreas R. Nat Commun Article Cells set up contractile actin arrays to drive various shape changes and to exert forces to their environment. To understand their assembly process, we present here a reconstituted contractile system, comprising F-actin and myosin II filaments, where we can control the local activation of myosin by light. By stimulating different symmetries, we show that the force balancing at the boundaries determine the shape changes as well as the dynamics of the global contraction. Spatially anisotropic attachment of initially isotropic networks leads to a self-organization of highly aligned contractile fibres, being reminiscent of the order formation in muscles or stress fibres. The observed shape changes and dynamics are fully recovered by a minimal physical model. Nature Publishing Group 2016-10-14 /pmc/articles/PMC5067607/ /pubmed/27739426 http://dx.doi.org/10.1038/ncomms13120 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Schuppler, Matthias
Keber, Felix C.
Kröger, Martin
Bausch, Andreas R.
Boundaries steer the contraction of active gels
title Boundaries steer the contraction of active gels
title_full Boundaries steer the contraction of active gels
title_fullStr Boundaries steer the contraction of active gels
title_full_unstemmed Boundaries steer the contraction of active gels
title_short Boundaries steer the contraction of active gels
title_sort boundaries steer the contraction of active gels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067607/
https://www.ncbi.nlm.nih.gov/pubmed/27739426
http://dx.doi.org/10.1038/ncomms13120
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