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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2017
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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. |
format | Online Article Text |
id | pubmed-5501213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT fritzschemarco selforganizingactinpatternsshapecytoskeletalcortexorganization |