IL-2 and IL-15 manifest opposing effects on activation of nuclear factor of activated T cells

被引:7
|
作者
Eicher, DM [1 ]
机构
[1] Case Western Reserve Univ, Univ Hosp Cleveland, Sch Med, Div Hematol Oncol, Cleveland, OH 44106 USA
关键词
interleukin-2; interleukin-15; cytokine receptors; T cell receptor; signal transduction; nuclear factor of activated T cells (NF-AT); homeostasis; transcription factors;
D O I
10.1016/S0008-8749(03)00168-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
IL-2 and IL-15 are cytokines involved in T cell activation and death. Their non-shared receptors, IL-2Ralpha and IL-15Ralpha, are important in the homeostasis of lymphocytes as evidenced by gene deletion studies. How these cytokine/receptor systems affect T cell antigen receptor signaling pathways is poorly understood. Here, we show that the IL-2 and IL-15 cytokine/receptor a systems regulate activation of nuclear factor of activated T cells (NF-AT) in opposing ways. IL-15Ralpha increased while IL-2Ralpha decreased basal NF-AT activation status in a Jurkat transient transfection model. The effect of each of the a chain receptors on NF-AT activation was further opposed by addition of the respective cytokine. These effects were inhibited by anti-cytokine and anti-cytokine receptor reagents as well as by inhibitors of TCR signaling. These results suggest a novel pathway of cytokine action to regulate T cell signaling, activation, death, and homeostasis. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 142
页数:10
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