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Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics

Productive protrusions allowing motile cells to sense and migrate toward a chemotactic gradient of reactive oxygen species (ROS) require a tight control of the actin cytoskeleton. However, the mechanisms of how ROS affect cell protrusion and actin dynamics are not well elucidated yet. We show here t...

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Detalles Bibliográficos
Autores principales: Taulet, Nicolas, Delorme-Walker, Violaine D., DerMardirossian, Céline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410878/
https://www.ncbi.nlm.nih.gov/pubmed/22876286
http://dx.doi.org/10.1371/journal.pone.0041342
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author Taulet, Nicolas
Delorme-Walker, Violaine D.
DerMardirossian, Céline
author_facet Taulet, Nicolas
Delorme-Walker, Violaine D.
DerMardirossian, Céline
author_sort Taulet, Nicolas
collection PubMed
description Productive protrusions allowing motile cells to sense and migrate toward a chemotactic gradient of reactive oxygen species (ROS) require a tight control of the actin cytoskeleton. However, the mechanisms of how ROS affect cell protrusion and actin dynamics are not well elucidated yet. We show here that ROS induce the formation of a persistent protrusion. In migrating epithelial cells, protrusion of the leading edge requires the precise regulation of the lamellipodium and lamella F-actin networks. Using fluorescent speckle microscopy, we showed that, upon ROS stimulation, the F-actin retrograde flow is enhanced in the lamellipodium. This event coincides with an increase of cofilin activity, free barbed ends formation, Arp2/3 recruitment, and ERK activity at the cell edge. In addition, we observed an acceleration of the F-actin flow in the lamella of ROS-stimulated cells, which correlates with an enhancement of the cell contractility. Thus, this study demonstrates that ROS modulate both the lamellipodium and the lamella networks to control protrusion efficiency.
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spelling pubmed-34108782012-08-08 Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics Taulet, Nicolas Delorme-Walker, Violaine D. DerMardirossian, Céline PLoS One Research Article Productive protrusions allowing motile cells to sense and migrate toward a chemotactic gradient of reactive oxygen species (ROS) require a tight control of the actin cytoskeleton. However, the mechanisms of how ROS affect cell protrusion and actin dynamics are not well elucidated yet. We show here that ROS induce the formation of a persistent protrusion. In migrating epithelial cells, protrusion of the leading edge requires the precise regulation of the lamellipodium and lamella F-actin networks. Using fluorescent speckle microscopy, we showed that, upon ROS stimulation, the F-actin retrograde flow is enhanced in the lamellipodium. This event coincides with an increase of cofilin activity, free barbed ends formation, Arp2/3 recruitment, and ERK activity at the cell edge. In addition, we observed an acceleration of the F-actin flow in the lamella of ROS-stimulated cells, which correlates with an enhancement of the cell contractility. Thus, this study demonstrates that ROS modulate both the lamellipodium and the lamella networks to control protrusion efficiency. Public Library of Science 2012-08-02 /pmc/articles/PMC3410878/ /pubmed/22876286 http://dx.doi.org/10.1371/journal.pone.0041342 Text en © 2012 This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Taulet, Nicolas
Delorme-Walker, Violaine D.
DerMardirossian, Céline
Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics
title Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics
title_full Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics
title_fullStr Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics
title_full_unstemmed Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics
title_short Reactive Oxygen Species Regulate Protrusion Efficiency by Controlling Actin Dynamics
title_sort reactive oxygen species regulate protrusion efficiency by controlling actin dynamics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410878/
https://www.ncbi.nlm.nih.gov/pubmed/22876286
http://dx.doi.org/10.1371/journal.pone.0041342
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