Barberis, D., Casazza, A., Sordella, R., Corso, S., Artigiani, S., Settleman, J., Comoglio, P. M., Tamagnone, L.
(October 2005)
p190 Rho-GTPase activating protein associates with plexins and it is required for semaphorin signalling.
Journal of Cell Science, 118 (Pt 20).
pp. 4689-700.
ISSN 0021-9533
Abstract
Plexins are transmembrane receptors for semaphorins, guiding cell migration and axon extension. Plexin activation leads to the disassembly of integrin-based focal adhesive structures and to actin cytoskeleton remodelling and inhibition of cell migration; however, the underlying molecular mechanisms are unclear. We consistently observe a transient decrease of cellular RhoA-GTP levels upon plexin activation in adherent cells. One of the main effectors of RhoA downregulation is p190, a ubiquitously expressed GTPase activating protein (GAP). We show that, in p190-deficient fibroblasts, the typical functional activities mediated by plexins (such as cell collapse and inhibition of integrin-based adhesion) are blocked or greatly impaired. Notably, the functional response can be rescued in these cells by re-expressing exogenous p190, but not a mutant form specifically lacking RhoGAP activity. We furthermore demonstrate that semaphorin function is blocked in epithelial cells, primary endothelial cells and neuroblasts upon treatment with small interfering RNAs that knockdown p190 expression. Finally, we show that p190 transiently associates with plexins, and its RhoGAP activity is increased in response to semaphorin stimulation. We conclude that p190-RhoGAP is crucially involved in semaphorin signalling to the actin cytoskeleton, via interaction with plexins.
Item Type: |
Paper
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Uncontrolled Keywords: |
Animals
Antigens, CD pharmacology
Carrier Proteins metabolism
Cell Adhesion drug effects
Cell Movement drug effects
Chemotaxis
DNA-Binding Proteins
Down-Regulation genetics
Endothelial Cells cytology
Epithelial Cells cytology drug effects
Fibroblasts cytology drug effects
Focal Adhesions
GTPase-Activating Proteins metabolism
Guanine Nucleotide Exchange Factors
Humans
Intracellular Signaling Peptides and Proteins
Mice
NIH 3T3 Cells
Nerve Growth Factor pharmacology
Neurites
PC12 Cells
Protein Binding
RNA, Small Interfering genetics
Rats
Receptors, Cell Surface metabolism
Repressor Proteins
Semaphorins metabolism pharmacologRHo
Signal Transduction |
Subjects: |
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification bioinformatics > genomics and proteomics > genetics & nucleic acid processing bioinformatics > genomics and proteomics bioinformatics > genomics and proteomics > genetics & nucleic acid processing > protein structure, function, modification > protein types > actin organs, tissues, organelles, cell types and functions > cell types and functions > cell types organs, tissues, organelles, cell types and functions > cell types and functions > cell types organs, tissues, organelles, cell types and functions > cell types and functions > cell types organs, tissues, organelles, cell types and functions > cell types and functions organs, tissues, organelles, cell types and functions > cell types and functions > cell types > epithelial cell organs, tissues, organelles, cell types and functions > cell types and functions > cell types > epithelial cell organs, tissues, organelles, cell types and functions > cell types and functions > cell types > epithelial cell organs, tissues, organelles, cell types and functions > tissues types and functions > membranes bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > siRNA |
CSHL Authors: |
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Communities: |
CSHL labs > Sordella lab |
Depositing User: |
CSHL Librarian
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Date: |
15 October 2005 |
Date Deposited: |
17 Jan 2012 16:06 |
Last Modified: |
13 Mar 2013 16:00 |
Related URLs: |
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URI: |
https://repository.cshl.edu/id/eprint/22532 |
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