Fyn can partially substitute for Lck in T lymphocyte development

被引:188
作者
Groves, T
Smiley, P
Cooke, MP
Forbush, K
Perlmutter, RM
Guidos, CJ
机构
[1] HOSP SICK CHILDREN,RES INST,DIV IMMUNOL & CANC,TORONTO,ON M5G 1X8,CANADA
[2] UNIV TORONTO,DEPT IMMUNOL,TORONTO,ON M5S 1A8,CANADA
[3] UNIV WASHINGTON,DEPT BIOCHEM,SEATTLE,WA 98195
[4] UNIV WASHINGTON,DEPT IMMUNOL,SEATTLE,WA 98195
[5] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98195
[6] UNIV WASHINGTON,HOWARD HUGHES MED INST,SEATTLE,WA 98195
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1074-7613(00)80498-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lck, a Src family tyrosine kinase, transduces signals important for the development of alpha beta and gamma delta T cells. However, T cell development is only partially compromised in Lck-deficient mice, suggesting that other kinases may also transduce pre-TCR or TCR signals. One candidate is Fyn, a Src kinase coexpressed with Lck in immature and mature T cells. Here we show that T cell development is completely compromised in lck(-/-)fyn(-/-) mice. In addition, we demonstrate that expression of a gain-of-function mutant fyn(T) transgene completely restores production of immature CD4/CD8 double positive thymocytes and gamma delta T cells and improves the representation of CD4 or CD8 single positive thymocytes. These observations reveal that Fyn can subserve some Lck-like functions in T cell development.
引用
收藏
页码:417 / 428
页数:12
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