Control of lymphocyte shape and the chemotactic response by the GTP exchange factor Vav
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Rho GTPases control many facets of cell polarity and migration; namely, the reorganization of the cellular cytoskeleton to extracellular stimuli. Rho GTPases are activated by GTP exchange factors (GEFs), which induce guanosine diphosphate (GDP) release and the stabilization of the nucleotide-free state. Thus, the role of GEFs in the regulation of the cellular response to extracellular cues during cell migration is a critical step of this process. In this report, we have analyzed the activation and subcellular localization of the hematopoietic GEF Vav in human peripheral blood lymphocytes stimulated with the chemokine stromal cell-derived factor-1 (SDF-1α). We show a robust activation of Vav and its redistribution to motility-associated subcellular structures, and we provide biochemical evidence of the recruitment of Vav to the membrane of SDF-1α-activated human lymphocytes, where it transiently interacts with the SDF-1α receptor CXCR4. Overexpression of a dominant negative form of Vav abolished lymphocyte polarization, actin polymerization, and migration. SDF-1α-mediated cell polarization and migration also were impaired by overexpression of an active, oncogenic Vav, although the mechanism appears to be different. Together, our data postulate a pivotal role for Vav in the transmission of the migratory signal through the chemokine receptor CXCR4. © 2005 by The American Society of Hematology.
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chemokine; stromal cell derived factor 1; Vav protein; actin polymerization; animal cell; article; cell activation; cell migration; cell motility; cell polarity; cell size; cell stimulation; cellular distribution; chemotaxis; controlled study; gene overexpression; human; human cell; lymphocyte; lymphocyte activation; mouse; nonhuman; peripheral lymphocyte; priority journal; signal transduction; Animals; Cell Cycle Proteins; Cell Polarity; Cell Shape; Chemokines, CXC; Chemotaxis, Leukocyte; Gene Expression; Humans; Lymphocytes; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-vav; Receptors, CXCR4; Signal Transduction
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