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Self-organizing actin patterns shape cytoskeletal cortex organization

Living systems rely, for biological function, on the spatiotemporal organization of their structures. Cellular order naturally emerges by dissipation of energy. Consequently, energy-consuming processes operating far from thermodynamic equilibrium are a necessary condition to enable biological system...

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Detalles Bibliográficos
Autor principal: Fritzsche, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501213/
https://www.ncbi.nlm.nih.gov/pubmed/28702125
http://dx.doi.org/10.1080/19420889.2017.1303591
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author Fritzsche, Marco
author_facet Fritzsche, Marco
author_sort Fritzsche, Marco
collection PubMed
description Living systems rely, for biological function, on the spatiotemporal organization of their structures. Cellular order naturally emerges by dissipation of energy. Consequently, energy-consuming processes operating far from thermodynamic equilibrium are a necessary condition to enable biological systems to respond to environmental cues that allow their transitions between different steady-states. Such self-organization was predicted for the actin cytoskeleton in theoretical considerations and has repeatedly been observed in cell-free systems. We now demonstrate in our recent work how self-organizing actin patterns such as vortices, stars, and asters may allow cells to adjust their membrane architecture without affecting their cell mechanical properties.
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spelling pubmed-55012132017-07-12 Self-organizing actin patterns shape cytoskeletal cortex organization Fritzsche, Marco Commun Integr Biol Short Communication Living systems rely, for biological function, on the spatiotemporal organization of their structures. Cellular order naturally emerges by dissipation of energy. Consequently, energy-consuming processes operating far from thermodynamic equilibrium are a necessary condition to enable biological systems to respond to environmental cues that allow their transitions between different steady-states. Such self-organization was predicted for the actin cytoskeleton in theoretical considerations and has repeatedly been observed in cell-free systems. We now demonstrate in our recent work how self-organizing actin patterns such as vortices, stars, and asters may allow cells to adjust their membrane architecture without affecting their cell mechanical properties. Taylor & Francis 2017-04-27 /pmc/articles/PMC5501213/ /pubmed/28702125 http://dx.doi.org/10.1080/19420889.2017.1303591 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Short Communication
Fritzsche, Marco
Self-organizing actin patterns shape cytoskeletal cortex organization
title Self-organizing actin patterns shape cytoskeletal cortex organization
title_full Self-organizing actin patterns shape cytoskeletal cortex organization
title_fullStr Self-organizing actin patterns shape cytoskeletal cortex organization
title_full_unstemmed Self-organizing actin patterns shape cytoskeletal cortex organization
title_short Self-organizing actin patterns shape cytoskeletal cortex organization
title_sort self-organizing actin patterns shape cytoskeletal cortex organization
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501213/
https://www.ncbi.nlm.nih.gov/pubmed/28702125
http://dx.doi.org/10.1080/19420889.2017.1303591
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