Genetic and biochemical evidence for a critical role of janus kinase (JAK)-3 in mast cell-mediated type I hypersensitivity reactions

被引:37
作者
Malaviya, R
Uckun, FM
机构
[1] Howard Hughes Med Inst, Dept Allergy, St Paul, MN 55113 USA
[2] Howard Hughes Med Inst, Dept Immunol, St Paul, MN 55113 USA
[3] Howard Hughes Med Inst, Dept Drug Discovery Program, St Paul, MN 55113 USA
关键词
D O I
10.1006/bbrc.1999.0513
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the role of JAK3 in IgE receptor! Fc epsilon RI-mediated mast cell responses. IgE/antigen induced degranulation and mediator release were substantially reduced with Jak3(-/-) mast cells from JAK3-null mice that were generated by targeted disruption of Jak3 gene in embryonic stem cells. Further, treatment of mast cells with 3'bromo-4'-hydroxylphenyl)amino-6,7-dimethoxyquinazoline (WHI-P154), a potent inhibitor of JAK3, inhibited degranulation and proinflammatory mediator release after IgE receptor! Fc epsilon RI crosslinking. Thus, JAK3 plays a pivotal role in IgE receptor! Fc epsilon RI-mediated mast cell responses and targeting JAK3 may provide the basis for new and effective treatment as well as prevention programs for mast cell-mediated allergic reactions. (C) 1999 Academic Press.
引用
收藏
页码:807 / 813
页数:7
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