Journal
IMMUNITY
Volume 31, Issue 6, Pages 953-964Publisher
CELL PRESS
DOI: 10.1016/j.immuni.2009.09.021
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Funding
- Ministerio de Ciencia e Innovacion [SAF2005-02119, SAF2008-00479]
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Lymphocyte integrins mediate cell arrest on endothelium during immune surveillance after activation by chemokine-stimulated inside-out signals. Here we show that a Vav1-talin complex in T cells is a key target for chemokine-triggered inside-out signaling leading to integrin alpha 4 beta 1 activation. Thus, Vav1 dissociation from talin was required to generate high-affinity alpha 4 beta 1 conformations. Assembly of the Vav1-talin complex required PtdIns(4,5)P-2, which was provided by talin-bound phosphatidylinositol phosphate kinase I gamma. Chemokine-promoted Vav1 dissociation from talin followed an initial increase in talin binding to alpha 4 beta 1. This process was dependent on ZAP-70, which binds to and phosphorylates Vav1 in the complex, leading to further alpha 4 beta 1 activation and cell adhesion strengthening. Moreover, Vav1-talin dissociation was needed for Rac1 activation, thus indicating that alpha 4 beta 1 and Rac1 activation can be coupled by chemokine-stimulated ZAP-70 function. Our data suggest that Vav1 might function as a repressive adaptor of talin that must dissociate from alpha 4 beta 1-talin complexes for efficient integrin activation.
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