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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2017
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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. |
format | Online Article Text |
id | pubmed-5461013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT leduccecile regulationofmicrotubuleassociatedmotorsdrivesintermediatefilamentnetworkpolarization AT etiennemannevillesandrine regulationofmicrotubuleassociatedmotorsdrivesintermediatefilamentnetworkpolarization |