Vav GEFs regulate macrophage morphology and adhesion-induced Rac and Rho activation.

Exp Cell Res

King's College London, Randall Division of Cell and Molecular Biophysics, Guy's Campus, London, UK.

Published: November 2009

AI Article Synopsis

  • The Vav family of proteins serves as both signaling adapters and GEFs for Rho GTPases, playing a crucial role in regulating the cytoskeleton in various cell types.
  • Macrophages lacking all three Vav isoforms exhibit an elongated shape and increased mobility but do not show altered responses to the chemoattractant CSF-1.
  • Vav proteins are essential for adhesion-induced cell spreading and activation of RhoA and Rac1, influencing macrophage morphology and movement through their role in coupling adhesion receptors to these signaling pathways.

Article Abstract

The Vav family of proteins have the potential to act as both signalling adapters and GEFs for Rho GTPases. They have therefore been proposed as regulators of the cytoskeleton in various cell types. We have used macrophages from mice deficient in all three Vav isoforms to determine how their function affects cell morphology and migration. Macrophages lacking Vav proteins adopt an elongated morphology and have enhanced migratory persistence in culture. To investigate the pathways through which Vav proteins exert their effects we analysed the responses of macrophages to the chemoattractant CSF-1 and to adhesion. We found that morphological and signalling responses of macrophages to CSF-1 did not require Vav proteins. In contrast, adhesion-induced cell spreading, RhoA and Rac1 activation and cell signalling were all dependent on Vav proteins. We propose that Vav proteins affect macrophage morphology and motile behaviour by coupling adhesion receptors to Rac1 and RhoA activity and regulating adhesion signalling events such as paxillin and ERK1/2 phosphorylation by acting as adapters.

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Source
http://dx.doi.org/10.1016/j.yexcr.2009.08.010DOI Listing

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