RhoB regulates cell migration through altered focal adhesion dynamics

The Rho GTPase RhoB has been shown to affect cell migration, but how it does this is not clear. Here we show that cells depleted of RhoB by RNAi are rounded and have defects in Rac-mediated spreading and lamellipodium extension, although they have active membrane ruffling around the periphery. Deple...

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Main Authors: Vega, Francisco M., Colomba, Audrey, Reymond, Nicolas, Thomas, Mairian, Ridley, Anne J.
Format: Online
Language:English
Published: The Royal Society 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376739/
id pubmed-3376739
recordtype oai_dc
spelling pubmed-33767392012-06-21 RhoB regulates cell migration through altered focal adhesion dynamics Vega, Francisco M. Colomba, Audrey Reymond, Nicolas Thomas, Mairian Ridley, Anne J. Research The Rho GTPase RhoB has been shown to affect cell migration, but how it does this is not clear. Here we show that cells depleted of RhoB by RNAi are rounded and have defects in Rac-mediated spreading and lamellipodium extension, although they have active membrane ruffling around the periphery. Depletion of the exchange factor GEF-H1 induces a similar phenotype. RhoB-depleted cells migrate faster, but less persistently in a chemotactic gradient, and frequently round up during migration. RhoB-depleted cells have similar numbers of focal adhesions to control cells during spreading and migration, but show more diffuse and patchy contact with the substratum. They have lower levels of surface β1 integrin, and β1 integrin activity is reduced in actin-rich protrusions. We propose that RhoB contributes to directional cell migration by regulating β1 integrin surface levels and activity, thereby stabilizing lamellipodial protrusions. The Royal Society 2012-05 /pmc/articles/PMC3376739/ /pubmed/22724071 http://dx.doi.org/10.1098/rsob.120076 Text en http://creativecommons.org/licenses/by/3.0/ © 2012 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Vega, Francisco M.
Colomba, Audrey
Reymond, Nicolas
Thomas, Mairian
Ridley, Anne J.
spellingShingle Vega, Francisco M.
Colomba, Audrey
Reymond, Nicolas
Thomas, Mairian
Ridley, Anne J.
RhoB regulates cell migration through altered focal adhesion dynamics
author_facet Vega, Francisco M.
Colomba, Audrey
Reymond, Nicolas
Thomas, Mairian
Ridley, Anne J.
author_sort Vega, Francisco M.
title RhoB regulates cell migration through altered focal adhesion dynamics
title_short RhoB regulates cell migration through altered focal adhesion dynamics
title_full RhoB regulates cell migration through altered focal adhesion dynamics
title_fullStr RhoB regulates cell migration through altered focal adhesion dynamics
title_full_unstemmed RhoB regulates cell migration through altered focal adhesion dynamics
title_sort rhob regulates cell migration through altered focal adhesion dynamics
description The Rho GTPase RhoB has been shown to affect cell migration, but how it does this is not clear. Here we show that cells depleted of RhoB by RNAi are rounded and have defects in Rac-mediated spreading and lamellipodium extension, although they have active membrane ruffling around the periphery. Depletion of the exchange factor GEF-H1 induces a similar phenotype. RhoB-depleted cells migrate faster, but less persistently in a chemotactic gradient, and frequently round up during migration. RhoB-depleted cells have similar numbers of focal adhesions to control cells during spreading and migration, but show more diffuse and patchy contact with the substratum. They have lower levels of surface β1 integrin, and β1 integrin activity is reduced in actin-rich protrusions. We propose that RhoB contributes to directional cell migration by regulating β1 integrin surface levels and activity, thereby stabilizing lamellipodial protrusions.
publisher The Royal Society
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376739/
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