Tyrphostin AG-490 inhibits cytokine-mediated JAK3/STAT5a/b signal transduction and cellular proliferation of antigen-activated human T cells

被引:103
作者
Kirken, RA
Erwin, RA
Taub, D
Murphy, WJ
Behbod, F
Wang, LH
Pericle, F
Farrar, WL
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Integrat Biol & Pharmacol, Houston, TX 77030 USA
[2] Frederick Canc Res & Dev Ctr, SAIC Frederick, IRSP, Frederick, MD USA
[3] NIA, Immunol Lab, Baltimore, MD 21224 USA
[4] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
[5] NCI, Div Basic Sci,Cytokine Mol Mechanisms Sect, Mol Immunoregulat Lab, Frederick Canc Res & Dev Ctr, Frederick, MD 21701 USA
关键词
JAKs; Stats; kinase inhibitors; interleukin-2;
D O I
10.1002/jlb.65.6.891
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Janus kinase 3 (JAK3) is a cytoplasmic tyrosine kinase required for T cell development and activated by cytokines that utilize the interleukin-2 (IL-2) receptor common gamma chain (gamma(c)). Genetic inactivation of JAK3 is manifested as severe combined immunodeficiency disease (SCID) in humans and mice. These findings have suggested that JAK3 represents a pharmacological target to control certain lymphoid-derived diseases. Here we provide novel evidence that AG-490 potently inhibits the autokinase activity of JAK3 and tyrosine phosphorylation and DNA binding of signal transducer and activator of transcription 5a and 5b (STAT5a/b), Similar inhibitory effects were observed with other cytokines that use gamma(c). AG-490 also inhibited IL-2-mediated proliferative growth in human T cells with an IC50 = 25 mu M that was partially recoverable. Moreover, we demonstrate that this inhibitor prevented tetanus toroid antigen-specific T cell proliferation and expansion but failed to block activation of Zap70 or p56Lck after anti-CD3 stimulation of human T cells. Taken together, these findings suggest that AG-490 inhibits the JAK3-mediated Type II signaling pathway but not the T cell receptor-derived Type I pathway and possesses therapeutic potential for T cell-derived pathologies such as graft-versus-host disease, allergy, and autoimmune disorders.
引用
收藏
页码:891 / 899
页数:9
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