The Ets transcription factor ERM is Th1-specific and induced by IL-12 through a Stat4-dependent pathway

被引:94
作者
Ouyang, W
Jacobson, NG
Bhattacharya, D
Gorham, JD
Fenoglio, D
Sha, WC
Murphy, TL
Murphy, KM [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Ctr Immunol, Howard Hughes Med Inst, St Louis, MO 63110 USA
[3] Univ Calif Berkeley, Dept Immunol, Berkeley, CA 94720 USA
关键词
D O I
10.1073/pnas.96.7.3888
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interleukin 12 (IL-12)-induced T helper 1 (Th1) development requires Stat4 activation. However, antigen-activated Th1 cells can produce interferon gamma (IFN-gamma) independently of IL-12 and Stat4 activation. Thus, in differentiated Th1 cells, factors regulated by IL-12 and Stat4 may be involved in IFN-gamma production. Using subtractive cloning, we identified ERM, an Ets transcription factor, to be a Th1-specific, IL-12-induced gene. IL-12-induction of ERM occurred in wild-type and Stat1-deficient, but not Stat4-deficient, T cells, suggesting ERM is Stat4-inducible. Retroviral expression of ERM did not restore IFN-gamma production in Stat4-deficient T cells, but augmented IFN-gamma expression in Stat4-heterozygous T cells. Ets factors frequently regulate transcription via cooperative interactions with other transcription factors, and ERM has been reported to cooperate with c-Jun, However, in the absence of other transcription factors, ERM augmented expression of an IFN-y reporter by only 2-fold. Thus, determining the requirement for ERM in Th1 development likely will require gene targeting.
引用
收藏
页码:3888 / 3893
页数:6
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