van Oers N S, Weiss A
Department of Medicine, University of California, San Francisco 94143, USA.
Semin Immunol. 1995 Aug;7(4):227-36. doi: 10.1006/smim.1995.0027.
The T- and B-cell receptor (TCR and BCR) signal transduction processes involve a coordinated interplay between two classes of non-receptor protein tyrosine kinases (PTKs), the Src-family and the Syk/ZAP-70 family of PTKs. Following antigen-receptor stimulation, the Src-family of PTKs mediate the phosphorylation of tyrosine residues contained in a signalling motif localized in the TCR and BCR subunits. The phosphorylation of this signalling motif recruits the Syk/ZAP-70 family of PTKs into the antigen receptor complex. This mechanism requires the tandem SH2 domains in ZAP-70 complexing to two critically spaced phosphotyrosine residues within the signalling motif. The clustering of Syk/ZAP-70 and cross-talk between this family and the Src-PTKs regulates subsequent signalling events that lead to a variety of cellular responses, such as antibody secretion, lymphokine production, cytolytic activity, proliferation, differentiation and cell survival.
T细胞和B细胞受体(TCR和BCR)信号转导过程涉及两类非受体蛋白酪氨酸激酶(PTK)——Src家族和Syk/ZAP-70家族PTK之间的协同相互作用。抗原受体受到刺激后,Src家族PTK介导位于TCR和BCR亚基中一个信号基序内的酪氨酸残基磷酸化。该信号基序的磷酸化将Syk/ZAP-70家族PTK招募到抗原受体复合物中。此机制要求ZAP-70中的串联SH2结构域与信号基序内两个关键间隔的磷酸酪氨酸残基结合。Syk/ZAP-70的聚集以及该家族与Src-PTK之间的相互作用调节随后的信号事件,这些事件导致多种细胞反应,如抗体分泌、淋巴因子产生、溶细胞活性、增殖、分化和细胞存活。