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Focal adhesions are hotspots for keratin filament precursor formation

Recent studies showed that keratin filament (KF) formation originates primarily from sites close to the actin-rich cell cortex. To further characterize these sites, we performed multicolor fluorescence imaging of living cells and found drastically increased KF assembly in regions of elevated actin t...

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Detalles Bibliográficos
Autores principales: Windoffer, Reinhard, Kölsch, Anne, Wöll, Stefan, Leube, Rudolf E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063835/
https://www.ncbi.nlm.nih.gov/pubmed/16682525
http://dx.doi.org/10.1083/jcb.200511124
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author Windoffer, Reinhard
Kölsch, Anne
Wöll, Stefan
Leube, Rudolf E.
author_facet Windoffer, Reinhard
Kölsch, Anne
Wöll, Stefan
Leube, Rudolf E.
author_sort Windoffer, Reinhard
collection PubMed
description Recent studies showed that keratin filament (KF) formation originates primarily from sites close to the actin-rich cell cortex. To further characterize these sites, we performed multicolor fluorescence imaging of living cells and found drastically increased KF assembly in regions of elevated actin turnover, i.e., in lamellipodia. Abundant KF precursors (KFPs) appeared within these areas at the distal tips of actin stress fibers, moving alongside the stress fibers until their integration into the peripheral KF network. The earliest KFPs were detected next to actin-anchoring focal adhesions (FAs) and were only seen after the establishment of FAs in emerging lamellipodia. Tight spatiotemporal coupling of FAs and KFP formation were not restricted to epithelial cells, but also occurred in nonepithelial cells and cells producing mutant keratins. Finally, interference with FA formation by talin short hairpin RNA led to KFP depletion. Collectively, our results support a major regulatory function of FAs for KF assembly, thereby providing the basis for coordinated shaping of the entire cytoskeleton during cell relocation and rearrangement.
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spelling pubmed-20638352007-11-29 Focal adhesions are hotspots for keratin filament precursor formation Windoffer, Reinhard Kölsch, Anne Wöll, Stefan Leube, Rudolf E. J Cell Biol Research Articles Recent studies showed that keratin filament (KF) formation originates primarily from sites close to the actin-rich cell cortex. To further characterize these sites, we performed multicolor fluorescence imaging of living cells and found drastically increased KF assembly in regions of elevated actin turnover, i.e., in lamellipodia. Abundant KF precursors (KFPs) appeared within these areas at the distal tips of actin stress fibers, moving alongside the stress fibers until their integration into the peripheral KF network. The earliest KFPs were detected next to actin-anchoring focal adhesions (FAs) and were only seen after the establishment of FAs in emerging lamellipodia. Tight spatiotemporal coupling of FAs and KFP formation were not restricted to epithelial cells, but also occurred in nonepithelial cells and cells producing mutant keratins. Finally, interference with FA formation by talin short hairpin RNA led to KFP depletion. Collectively, our results support a major regulatory function of FAs for KF assembly, thereby providing the basis for coordinated shaping of the entire cytoskeleton during cell relocation and rearrangement. The Rockefeller University Press 2006-05-08 /pmc/articles/PMC2063835/ /pubmed/16682525 http://dx.doi.org/10.1083/jcb.200511124 Text en Copyright © 2006, The Rockefeller University Press 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 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Windoffer, Reinhard
Kölsch, Anne
Wöll, Stefan
Leube, Rudolf E.
Focal adhesions are hotspots for keratin filament precursor formation
title Focal adhesions are hotspots for keratin filament precursor formation
title_full Focal adhesions are hotspots for keratin filament precursor formation
title_fullStr Focal adhesions are hotspots for keratin filament precursor formation
title_full_unstemmed Focal adhesions are hotspots for keratin filament precursor formation
title_short Focal adhesions are hotspots for keratin filament precursor formation
title_sort focal adhesions are hotspots for keratin filament precursor formation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063835/
https://www.ncbi.nlm.nih.gov/pubmed/16682525
http://dx.doi.org/10.1083/jcb.200511124
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