Matuszyk J, Kałas W, Kozicki R, Strzadała L
Laboratorium Immunologii Komórkowej, Instytutu Immunologii i Terapii Doświadczalnej PAN, Wrocławiu.
Postepy Hig Med Dosw. 1999;53(4):531-43.
On the basis of recent reports we discuss the role of Vav in TCR-dependent signaling pathways. The Vav protein is GDP/GTP exchange factor for Rac, which initiates transduction of signals in JNK pathway. Upon stimulation of TCR by antigenic peptides, Vav associates with Zap-70 in TCR/CD3 signaling complex and becomes phosphorylated on Tyr-174 by tyrosine kinase Lck. The function of Vav is modulated by substrates and products of PI3-kinase activated by interaction of CD28 on thymocytes with B7 on antigen presenting cells. The PI3-kinase substrates inhibit activation of Vav, while the products enhance phosphorylation and activation of Vav by Lck. It seems that Vav functions in key point of TCR-mediated signaling pathway, which is regulated by costimulatory molecule (CD28) necessary for negative selection. The Vav-mediated integration of signals results in positive or negative selection of thymocytes.
基于近期的报道,我们讨论了Vav在TCR依赖性信号通路中的作用。Vav蛋白是Rac的GDP/GTP交换因子,可启动JNK通路中的信号转导。当抗原肽刺激TCR时,Vav与TCR/CD3信号复合物中的Zap-70结合,并被酪氨酸激酶Lck在Tyr-174位点磷酸化。Vav的功能受PI3激酶底物和产物的调节,PI3激酶由胸腺细胞上的CD28与抗原呈递细胞上的B7相互作用激活。PI3激酶底物抑制Vav的激活,而其产物则增强Lck对Vav的磷酸化和激活作用。Vav似乎在TCR介导的信号通路的关键点发挥作用,该通路受阴性选择所必需的共刺激分子(CD28)调控。Vav介导的信号整合导致胸腺细胞的阳性或阴性选择。