The Src family tyrosine kinase Fyn regulates natural killer T cell development

被引:157
作者
Gadue, P
Morton, N
Stein, PL
机构
[1] Wistar Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Grad Program Immunol, Philadelphia, PA 19104 USA
关键词
signal transduction; mouse mutants; Lck; beta; 2-microglobulin; CD1;
D O I
10.1084/jem.190.8.1189
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T lymphocytes express two Src tyrosine kinases, Lck and Fyn. While thymocyte and T cell subsets are largely normal in fyn(-/-) mice, animals lacking Lck have impaired T cell development. Here, it is shown that Fyn is required for the rapid burst of interleukin (IL)-4 and IL-13 synthesis, which occurs promptly after T cell receptor activation. The lack of cytokine induction in fyn mutant mice is due to a block In natural killer (NK) T cell development. Studies using bone marrow chimeras indicate that the defect behaves in a cell-autonomous manner, and the lack of NK T cells is probably not caused by inappropriate microenvironmental cues. Both NK T cells and conventional T cells express similar levels of Lck, implying that Fyn and Lck have distinct roles in regulating NK T cell ontogeny. The fyn mutation defines the first signaling molecule that is selectively required for NK T cell, but not for T lymphocyte or NK cell development.
引用
收藏
页码:1189 / 1195
页数:7
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