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The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction
Cells continuously sense and respond to external mechanical forces through their cytoskeleton. Here we show that only a small subset of actin fibers, those forming the perinuclear actin cap that wraps around the nucleus, form in response to low physiological mechanical stresses in adherent fibroblas...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548190/ https://www.ncbi.nlm.nih.gov/pubmed/23336069 http://dx.doi.org/10.1038/srep01087 |
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author | Chambliss, Allison B. Khatau, Shyam B. Erdenberger, Nicholas Robinson, D. Kyle Hodzic, Didier Longmore, Gregory D. Wirtz, Denis |
author_facet | Chambliss, Allison B. Khatau, Shyam B. Erdenberger, Nicholas Robinson, D. Kyle Hodzic, Didier Longmore, Gregory D. Wirtz, Denis |
author_sort | Chambliss, Allison B. |
collection | PubMed |
description | Cells continuously sense and respond to external mechanical forces through their cytoskeleton. Here we show that only a small subset of actin fibers, those forming the perinuclear actin cap that wraps around the nucleus, form in response to low physiological mechanical stresses in adherent fibroblasts. While conventional basal stress fibers form only past a threshold shear stress of 0.5 dyn/cm(2), actin-cap fibers are formed at shear stresses 50 times lower and orders-of-magnitude faster than biochemical stimulation. This fast differential response is uniquely mediated by focal adhesion protein zyxin at low shear stress and actomyosin fibers of the actin cap. We identify additional roles for lamin A/C of the nuclear lamina and linkers of nucleus to cytoskeleton (LINC) molecules nesprin2giant and nesprin3, which anchor actin cap fibers to the nucleus. These results suggest an interconnected physical pathway for mechanotransduction, from the extracellular milieu to the nucleus. |
format | Online Article Text |
id | pubmed-3548190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-35481902013-01-18 The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction Chambliss, Allison B. Khatau, Shyam B. Erdenberger, Nicholas Robinson, D. Kyle Hodzic, Didier Longmore, Gregory D. Wirtz, Denis Sci Rep Article Cells continuously sense and respond to external mechanical forces through their cytoskeleton. Here we show that only a small subset of actin fibers, those forming the perinuclear actin cap that wraps around the nucleus, form in response to low physiological mechanical stresses in adherent fibroblasts. While conventional basal stress fibers form only past a threshold shear stress of 0.5 dyn/cm(2), actin-cap fibers are formed at shear stresses 50 times lower and orders-of-magnitude faster than biochemical stimulation. This fast differential response is uniquely mediated by focal adhesion protein zyxin at low shear stress and actomyosin fibers of the actin cap. We identify additional roles for lamin A/C of the nuclear lamina and linkers of nucleus to cytoskeleton (LINC) molecules nesprin2giant and nesprin3, which anchor actin cap fibers to the nucleus. These results suggest an interconnected physical pathway for mechanotransduction, from the extracellular milieu to the nucleus. Nature Publishing Group 2013-01-18 /pmc/articles/PMC3548190/ /pubmed/23336069 http://dx.doi.org/10.1038/srep01087 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Chambliss, Allison B. Khatau, Shyam B. Erdenberger, Nicholas Robinson, D. Kyle Hodzic, Didier Longmore, Gregory D. Wirtz, Denis The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
title | The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
title_full | The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
title_fullStr | The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
title_full_unstemmed | The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
title_short | The LINC-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
title_sort | linc-anchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548190/ https://www.ncbi.nlm.nih.gov/pubmed/23336069 http://dx.doi.org/10.1038/srep01087 |
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