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T细胞受体相关的CD3-ε蛋白在T细胞活化时,其保守信号转导基序的两个酪氨酸残基会发生磷酸化。

The T cell receptor associated CD3-epsilon protein is phosphorylated upon T cell activation in the two tyrosine residues of a conserved signal transduction motif.

作者信息

Sancho J, Franco R, Chatila T, Hall C, Terhorst C

机构信息

Division of Immunology, Beth Israel Hospital, Boston, MA 02215.

出版信息

Eur J Immunol. 1993 Jul;23(7):1636-42. doi: 10.1002/eji.1830230736.

Abstract

Signal transduction through the T cell receptor for antigen, the TcR/CD3 complex, involves phosphorylation of tyrosine residues in the CD3-zeta chain. Since both CD3-epsilon and the zeta chain contain a tyrosine-based signaling motif, we examine phosphorylation of CD3-epsilon in human T cells. Engagement of the TcR/CD3 complex induced tyrosine phosphorylation of CD3-epsilon in vivo. Induction of CD3-epsilon phosphorylation followed similar kinetics to that of the zeta chain phosphorylation. In contrast to zeta, CD3-epsilon phosphorylation was strictly dependent upon cell surface expression of this member of the TcR/CD3 complex. Chemical and proteolytic cleavage combined with peptide-specific Western blotting established that CD3-epsilon phosphorylation occurred in the two tyrosine residues located in the signal transduction motif in the C-terminal portion of the molecule. Taken together, these data indicated that phosphorylation of CD3-epsilon by tyrosine protein kinases may serve to couple the TcR/CD3 complex to other effector molecules in the signaling cascade.

摘要

通过抗原T细胞受体(TcR)/CD3复合物进行的信号转导涉及CD3ζ链中酪氨酸残基的磷酸化。由于CD3ε和ζ链都含有基于酪氨酸的信号基序,我们研究了人T细胞中CD3ε的磷酸化情况。TcR/CD3复合物的激活在体内诱导了CD3ε的酪氨酸磷酸化。CD3ε磷酸化的诱导动力学与ζ链磷酸化相似。与ζ链不同,CD3ε的磷酸化严格依赖于TcR/CD3复合物该成员的细胞表面表达。化学和蛋白水解切割结合肽特异性蛋白质印迹法证实,CD3ε磷酸化发生在分子C端信号转导基序中的两个酪氨酸残基上。综上所述,这些数据表明酪氨酸蛋白激酶对CD3ε的磷酸化可能有助于在信号级联反应中将TcR/CD3复合物与其他效应分子偶联起来。

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