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Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia

Epithelia are exposed to multiple forms of stress. Keratin intermediate filaments are abundant in epithelia and form cytoskeletal networks that contribute to cell type–specific functions, such as adhesion, migration, and metabolism. A perpetual keratin filament turnover cycle supports these function...

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Detalles Bibliográficos
Autores principales: Windoffer, Reinhard, Beil, Michael, Magin, Thomas M., Leube, Rudolf E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171125/
https://www.ncbi.nlm.nih.gov/pubmed/21893596
http://dx.doi.org/10.1083/jcb.201008095
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author Windoffer, Reinhard
Beil, Michael
Magin, Thomas M.
Leube, Rudolf E.
author_facet Windoffer, Reinhard
Beil, Michael
Magin, Thomas M.
Leube, Rudolf E.
author_sort Windoffer, Reinhard
collection PubMed
description Epithelia are exposed to multiple forms of stress. Keratin intermediate filaments are abundant in epithelia and form cytoskeletal networks that contribute to cell type–specific functions, such as adhesion, migration, and metabolism. A perpetual keratin filament turnover cycle supports these functions. This multistep process keeps the cytoskeleton in motion, facilitating rapid and protein biosynthesis–independent network remodeling while maintaining an intact network. The current challenge is to unravel the molecular mechanisms underlying the regulation of the keratin cycle in relation to actin and microtubule networks and in the context of epithelial tissue function.
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spelling pubmed-31711252012-03-05 Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia Windoffer, Reinhard Beil, Michael Magin, Thomas M. Leube, Rudolf E. J Cell Biol Reviews Epithelia are exposed to multiple forms of stress. Keratin intermediate filaments are abundant in epithelia and form cytoskeletal networks that contribute to cell type–specific functions, such as adhesion, migration, and metabolism. A perpetual keratin filament turnover cycle supports these functions. This multistep process keeps the cytoskeleton in motion, facilitating rapid and protein biosynthesis–independent network remodeling while maintaining an intact network. The current challenge is to unravel the molecular mechanisms underlying the regulation of the keratin cycle in relation to actin and microtubule networks and in the context of epithelial tissue function. The Rockefeller University Press 2011-09-05 /pmc/articles/PMC3171125/ /pubmed/21893596 http://dx.doi.org/10.1083/jcb.201008095 Text en © 2011 Windoffer et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Reviews
Windoffer, Reinhard
Beil, Michael
Magin, Thomas M.
Leube, Rudolf E.
Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
title Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
title_full Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
title_fullStr Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
title_full_unstemmed Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
title_short Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
title_sort cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171125/
https://www.ncbi.nlm.nih.gov/pubmed/21893596
http://dx.doi.org/10.1083/jcb.201008095
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