Journal
MOLECULAR BIOLOGY OF THE CELL
Volume 16, Issue 7, Pages 3223-3235Publisher
AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E04-12-1049
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- NCI NIH HHS [R01CA7373503] Funding Source: Medline
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The chemokine CXCL12 promotes T lymphocyte adhesion mediated by the integrin alpha 4 beta 1. CXCL12 activates the GTPase Rac, as well as Vav1, a guanine-nucleotide exchange factor for Rac, concomitant with up-regulation of alpha 4 beta 1-dependent adhesion. Inhibition of CXCL12-promoted Rac and Vav1 activation by transfection of dominant negative Rac or Vav1 forms, or by transfection of their siRNA, remarkably impaired the increase in T lymphocyte attachment to alpha 4 beta 1 ligands in response to this chemokine. Importantly, inhibition of Vav1 expression by RNA interference resulted in a blockade of Rac activation in response to CXCL12. Adhesions in flow chambers and soluble binding assays using these transfectants indicated that initial ligand binding and adhesion strengthening mediated by alpha 4 beta 1 were dependent on Vav1 and Rac activation by CXCL12. Finally, CXCL12-promoted T-cell transendothelial migration involving alpha 4 beta 1-mediated adhesion was notably inhibited by expression of dominant negative Vav1 and Rac. These results indicate that activation of Vav1-Rac signaling pathway by CXCL12 represents an important inside-out event controlling efficient up-regulation of a4p1-dependent T lymphocyte adhesion.
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