Lyn tyrosine kinase: Accentuating the positive and the negative

被引:269
作者
Xu, YK
Harder, KW
Huntington, ND
Hibbs, ML
Tarlinton, DM [1 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[2] Ludwig Inst Canc Res, Melbourne, Vic 3050, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.immuni.2004.12.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lyn, one of several Src-family tyrosine kinases in immune cells, is noted for its ability to negatively regulate signaling pathways through phosphorylation of inhibitory receptors, enzymes, and adaptors. Somewhat paradoxically, it is also a key mediator in several pathways of B cell activation, such as CD19 and CD180. Whether Lyn functions to promote or inhibit immune cell activation depends on the stimulus and the developmental state, meaning that the consequences of Lyn activity are context dependent. The importance of regulating Lyn activity is exemplified by the pathological conditions that develop in both lyn(-/-) and lyn gain-of-function mice (lyn(up/up)), including lethal antibody-mediated autoimmune diseases and myeloid neoplasia. Here, we review the outcomes of altered Lyn activity within the framework of B cell development and differentiation and the circumstances that appear to dictate the outcome.
引用
收藏
页码:9 / 18
页数:10
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