期刊
JOURNAL OF EXPERIMENTAL MEDICINE
卷 197, 期 4, 页码 503-513出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20021498
关键词
CD3; CD5; T cell receptor; SH2 domain; Rac
The unique tyrosine kinase binding (TKB) domain of Cb1 targets phosphorylated tyrosines on activated protein tyrosine kinases (PTKs); this targeting is considered essential for Cb1 proteins to negatively regulate PTKs. Here, a loss-of-function mutation (G304E) in the c-Cb1 TKB domain, first identified in Caenorhabditis elegans, was introduced into a mouse and its effects in thymocytes and T cells were studied. In marked contrast to the c-Cb1 knockout mouse, we found no evidence of enhanced activity of the ZAP-70 PTK in thymocytes from the TKB domain mutant mouse. This finding contradicts the accepted mechanism of c-Cb1-mediated negative regulation, which requires TKB domain targeting of phosphotyrosine 292 in ZAP-70. However, the TKB domain mutant mouse does show aspects of enhanced signaling that parallel those of the c-Cb1 knockout mouse, but these involve the constitutive activation of Rac and not enhanced PTK activity. Furthermore, the enhanced signaling in CD4(+)CD8(+) double positive thymocytes appears to be compensated by the selective down-regulation of CD3 on mature thymocytes and peripheral T cells from both strains of mutant c-Cb1 mice.
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