CD4, CD8 AND THE TCR-CD3 COMPLEX - A NOVEL CLASS OF PROTEIN-TYROSINE KINASE RECEPTOR

被引:180
作者
RUDD, CE [1 ]
机构
[1] HARVARD UNIV,SCH MED,BOSTON,MA 02115
来源
IMMUNOLOGY TODAY | 1990年 / 11卷 / 11期
关键词
D O I
10.1016/0167-5699(90)90159-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A novel form of receptor-kinase interaction was first described in the interaction between the CD4 and CD8 antigens and the protein tyrosine kinase p56lck. This linkage, between a regulatory antigen on T cells and a member of a family of intracellular molecules with an established ability to activate and transform cells, is likely to be of great importance in the regulation of T-cell growth. Recently, data have been obtained on the molecular basis of regulation of the CD4/CD8-p56lck interaction and an interaction between the T-cell receptor complex (TCR-CD3) and another src-kinase p59fyn has been described. Here, Christopher Rudd examines these interactions and outlines their potential roles in normal and malignant T-cell growth. © 1990.
引用
收藏
页码:400 / 406
页数:7
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