Turner M, Mee P J, Walters A E, Quinn M E, Mellor A L, Zamoyska R, Tybulewicz V L
National Institute for Medical Research, The Ridgeway, London, United Kingdom.
Immunity. 1997 Oct;7(4):451-60. doi: 10.1016/s1074-7613(00)80367-2.
The T cell repertoire is shaped by positive and negative selection of thymocytes that express low levels of T cell receptor (TCR) and both CD4 and CD8. TCR-mediated signals that determine these selection processes are only partly understood. Vav, a GDP-GTP exchange factor for Rho-family proteins, is tyrosine phosphorylated following TCR stimulation, suggesting that it may transduce TCR signals. We now demonstrate that mice lacking Vav are viable and display a profound defect in the positive selection of both class I- and class II-restricted T cells. In contrast, Vav is not essential for negative selection, though in its absence negative selection is much less effective. Vav may influence the efficiency of TCR-induced selection events by regulating the intracellular calcium flux of thymocytes.
T细胞库是由表达低水平T细胞受体(TCR)以及CD4和CD8的胸腺细胞的阳性和阴性选择所塑造的。决定这些选择过程的TCR介导信号仅得到部分理解。Vav是一种Rho家族蛋白的GDP-GTP交换因子,在TCR刺激后会发生酪氨酸磷酸化,这表明它可能转导TCR信号。我们现在证明,缺乏Vav的小鼠是存活的,并且在I类和II类限制性T细胞的阳性选择中表现出严重缺陷。相比之下,Vav对于阴性选择并非必不可少,尽管在其缺失时阴性选择的效果要差得多。Vav可能通过调节胸腺细胞的细胞内钙通量来影响TCR诱导的选择事件的效率。