Rac GTPases play critical roles in early T-cell development

被引:61
作者
Dumont, Celine
Corsoni-Tadrzak, Agnieszka
Ruf, Sandra
de Boer, Jasper [3 ]
Williams, Adam [3 ]
Turner, Martin [2 ]
Kioussis, Dimitris [3 ]
Tybulewicz, Victor L. J. [1 ]
机构
[1] Natl Inst Med Res, Ridgeway, MRC, Div Immune Cell Biol, London NW7 1AA, England
[2] Babraham Inst, Cambridge, England
[3] Natl Inst Med Res, Div Mol Immunol, MRC, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
VAV-FAMILY PROTEINS; EXCHANGE FACTOR VAV; NF-KAPPA-B; RECEPTOR SIGNALS; TRANSGENIC MICE; NEGATIVE SELECTION; LYMPHOCYTE DEVELOPMENT; RHO GTPASES; ACTIVATION; THYMOCYTES;
D O I
10.1182/blood-2008-09-181180
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Rac1 and Rac2 GTPases play important roles in many processes including cytoskeletal reorganization, proliferation, and survival, and are required for B-cell development. Previous studies had shown that deficiency in Rac2 did not affect T-cell development, whereas the function of Rac1 in this process has not been investigated. We now show that simultaneous absence of both GTPases resulted in a very strong developmental block at the pre-TCR checkpoint and in defective positive selection. Unexpectedly, deficiency of Rac1 and Rac2 also resulted in the aberrant survival of thymocytes lacking expression of TCR beta, showing hallmarks of hyperactive Notch signaling. Furthermore, we found a similar novel phenotype in the absence of Vav1, Vav2, and Vav3, which function as guanine nucleotide exchange factors for Rac1 and Rac2. These results show that a pathway containing Vav and Rac proteins may negatively regulate Notch signaling during early thymic development. (Blood. 2009;113:3990-3998)
引用
收藏
页码:3990 / 3998
页数:9
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