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Talin as a mechanosensitive signaling hub

Cell adhesion to the extracellular matrix (ECM), mediated by transmembrane receptors of the integrin family, is exquisitely sensitive to biochemical, structural, and mechanical features of the ECM. Talin is a cytoplasmic protein consisting of a globular head domain and a series of α-helical bundles...

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Detalles Bibliográficos
Autores principales: Goult, Benjamin T., Yan, Jie, Schwartz, Martin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219721/
https://www.ncbi.nlm.nih.gov/pubmed/30254032
http://dx.doi.org/10.1083/jcb.201808061
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author Goult, Benjamin T.
Yan, Jie
Schwartz, Martin A.
author_facet Goult, Benjamin T.
Yan, Jie
Schwartz, Martin A.
author_sort Goult, Benjamin T.
collection PubMed
description Cell adhesion to the extracellular matrix (ECM), mediated by transmembrane receptors of the integrin family, is exquisitely sensitive to biochemical, structural, and mechanical features of the ECM. Talin is a cytoplasmic protein consisting of a globular head domain and a series of α-helical bundles that form its long rod domain. Talin binds to the cytoplasmic domain of integrin β-subunits, activates integrins, couples them to the actin cytoskeleton, and regulates integrin signaling. Recent evidence suggests switch-like behavior of the helix bundles that make up the talin rod domains, where individual domains open at different tension levels, exerting positive or negative effects on different protein interactions. These results lead us to propose that talin functions as a mechanosensitive signaling hub that integrates multiple extracellular and intracellular inputs to define a major axis of adhesion signaling.
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spelling pubmed-62197212019-05-05 Talin as a mechanosensitive signaling hub Goult, Benjamin T. Yan, Jie Schwartz, Martin A. J Cell Biol Reviews Cell adhesion to the extracellular matrix (ECM), mediated by transmembrane receptors of the integrin family, is exquisitely sensitive to biochemical, structural, and mechanical features of the ECM. Talin is a cytoplasmic protein consisting of a globular head domain and a series of α-helical bundles that form its long rod domain. Talin binds to the cytoplasmic domain of integrin β-subunits, activates integrins, couples them to the actin cytoskeleton, and regulates integrin signaling. Recent evidence suggests switch-like behavior of the helix bundles that make up the talin rod domains, where individual domains open at different tension levels, exerting positive or negative effects on different protein interactions. These results lead us to propose that talin functions as a mechanosensitive signaling hub that integrates multiple extracellular and intracellular inputs to define a major axis of adhesion signaling. Rockefeller University Press 2018-11-05 /pmc/articles/PMC6219721/ /pubmed/30254032 http://dx.doi.org/10.1083/jcb.201808061 Text en © 2018 Goult et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Reviews
Goult, Benjamin T.
Yan, Jie
Schwartz, Martin A.
Talin as a mechanosensitive signaling hub
title Talin as a mechanosensitive signaling hub
title_full Talin as a mechanosensitive signaling hub
title_fullStr Talin as a mechanosensitive signaling hub
title_full_unstemmed Talin as a mechanosensitive signaling hub
title_short Talin as a mechanosensitive signaling hub
title_sort talin as a mechanosensitive signaling hub
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219721/
https://www.ncbi.nlm.nih.gov/pubmed/30254032
http://dx.doi.org/10.1083/jcb.201808061
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