| Literature DB >> 11520460 |
J L Cannon1, C M Labno, G Bosco, A Seth, M H McGavin, K A Siminovitch, M K Rosen, J K Burkhardt.
Abstract
Cdc42 and WASP are critical regulators of actin polymerization whose function during T cell signaling is poorly understood. Using a novel reagent that specifically detects Cdc42-GTP in fixed cells, we found that activated Cdc42 localizes to the T cell:APC contact site in an antigen-dependent manner. TCR signaling alone was sufficient to induce localization of Cdc42-GTP, and functional Lck and Zap-70 kinases were required. WASP also localized to the T cell:APC contact site in an antigen-dependent manner. Surprisingly, WASP localization was independent of the Cdc42 binding domain but required the proline-rich domain. Our results indicate that localized WASP activation requires the integration of multiple signals: WASP is recruited via interaction with SH3 domain-containing proteins and is activated by Cdc42-GTP concentrated at the same site.Entities:
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Year: 2001 PMID: 11520460 DOI: 10.1016/s1074-7613(01)00178-9
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745