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[½»Á÷] Vav1 ºÍ Rac ͨ¹ýÕ³ºÏËØ¦Á4¦Â1¿ØÖÆÇ÷»¯Òò×Ó´Ù½øµÄTÁܰÍϸ°û𤸽

Control Chemokine-promoted T Lymphocyte Adhesion Mediated by the Integrin
David Garc¨ªa-Bernal *, Natalia Wright *, Elena Sotillo-Mallo et al


The chemokine CXCL12 promotes T lymphocyte adhesion mediated by the integrin ¦Á4¦Â1. CXCL12 activates the GTPase Rac, as well as Vav1, a guanine-nucleotide exchange factor for Rac, concomitant with up-regulation of ¦Á4¦Â1 -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 ¦Á4¦Â1 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 ¦Á4¦Â1 were dependent on Vav1 and Rac activation by CXCL12. Finally, CXCL12-promoted T-cell transendothelial migration involving ¦Á4¦Â1 -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 ¦Á4¦Â1 -dependent T lymphocyte adhesion.


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MBC Vol. 16, Issue 7, 3223-3235



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