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Regulation of microtubule-associated motors drives intermediate filament network polarization

Intermediate filaments (IFs) are key players in the control of cell morphology and structure as well as in active processes such as cell polarization, migration, and mechanoresponses. However, the regulatory mechanisms controlling IF dynamics and organization in motile cells are still poorly underst...

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Detalles Bibliográficos
Autores principales: Leduc, Cécile, Etienne-Manneville, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461013/
https://www.ncbi.nlm.nih.gov/pubmed/28432079
http://dx.doi.org/10.1083/jcb.201607045
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author Leduc, Cécile
Etienne-Manneville, Sandrine
author_facet Leduc, Cécile
Etienne-Manneville, Sandrine
author_sort Leduc, Cécile
collection PubMed
description Intermediate filaments (IFs) are key players in the control of cell morphology and structure as well as in active processes such as cell polarization, migration, and mechanoresponses. However, the regulatory mechanisms controlling IF dynamics and organization in motile cells are still poorly understood. In this study, we investigate the mechanisms leading to the polarized rearrangement of the IF network along the polarity axis. Using photobleaching and photoconversion experiments in glial cells expressing vimentin, glial fibrillary acidic protein, and nestin, we show that the distribution of cytoplasmic IFs results from a continuous turnover based on the cooperation of an actin-dependent retrograde flow and anterograde and retrograde microtubule-dependent transports. During wound-induced astrocyte polarization, IF transport becomes directionally biased from the cell center toward the cell front. Such asymmetry in the transport is mainly caused by a Cdc42- and atypical PKC–dependent inhibition of dynein-dependent retrograde transport. Our results show how polarity signaling can affect the dynamic turnover of the IF network to promote the polarization of the network itself.
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spelling pubmed-54610132017-12-05 Regulation of microtubule-associated motors drives intermediate filament network polarization Leduc, Cécile Etienne-Manneville, Sandrine J Cell Biol Research Articles Intermediate filaments (IFs) are key players in the control of cell morphology and structure as well as in active processes such as cell polarization, migration, and mechanoresponses. However, the regulatory mechanisms controlling IF dynamics and organization in motile cells are still poorly understood. In this study, we investigate the mechanisms leading to the polarized rearrangement of the IF network along the polarity axis. Using photobleaching and photoconversion experiments in glial cells expressing vimentin, glial fibrillary acidic protein, and nestin, we show that the distribution of cytoplasmic IFs results from a continuous turnover based on the cooperation of an actin-dependent retrograde flow and anterograde and retrograde microtubule-dependent transports. During wound-induced astrocyte polarization, IF transport becomes directionally biased from the cell center toward the cell front. Such asymmetry in the transport is mainly caused by a Cdc42- and atypical PKC–dependent inhibition of dynein-dependent retrograde transport. Our results show how polarity signaling can affect the dynamic turnover of the IF network to promote the polarization of the network itself. The Rockefeller University Press 2017-06-05 /pmc/articles/PMC5461013/ /pubmed/28432079 http://dx.doi.org/10.1083/jcb.201607045 Text en © 2017 Leduc and Etienne-Manneville 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 Research Articles
Leduc, Cécile
Etienne-Manneville, Sandrine
Regulation of microtubule-associated motors drives intermediate filament network polarization
title Regulation of microtubule-associated motors drives intermediate filament network polarization
title_full Regulation of microtubule-associated motors drives intermediate filament network polarization
title_fullStr Regulation of microtubule-associated motors drives intermediate filament network polarization
title_full_unstemmed Regulation of microtubule-associated motors drives intermediate filament network polarization
title_short Regulation of microtubule-associated motors drives intermediate filament network polarization
title_sort regulation of microtubule-associated motors drives intermediate filament network polarization
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461013/
https://www.ncbi.nlm.nih.gov/pubmed/28432079
http://dx.doi.org/10.1083/jcb.201607045
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