T-bet is a STAT1-induced regulator of IL-12R expression in naive CD4+ T cells

被引:793
作者
Afkarian, M
Sedy, JR
Yang, J
Jacobson, NG
Cereb, N
Yang, SY
Murphy, TL
Murphy, KM
机构
[1] Washington Univ, Sch Med, Howard Hughes Med Inst, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Histogenet Inc, Hawthorne, NY 10532 USA
[3] Ctr Genet Polymorphism, Hawthorne, NY 10532 USA
关键词
D O I
10.1038/ni794
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T helper type 1 (T(H)1) cell development involves interferon-gamma (IFN-gamma) signaling through signal transducer and activator of transcription 1 (STAT1) and interleukin-12 (IL-12) signaling through STAT4 activation. We examined here T-bet regulation and evaluated the actions of T-bet in STAT1- and STAT4-dependent T(H)1 development processes. We found that T-bet expression during T cell activation was strongly dependent on IFN-gamma signaling and STAT1 activation, but was independent of STAT4. Ectopic T-bet expression strongly increased IFN-gamma production in T(H)2 cells activated by PMA-ionomycin, but weakly increased IFN-gamma production in T(H)2 cells stimulated by IL-12-IL-18 or OVA peptide-antigen-presenting cell stimulation. In contrast, IL-12-IL-18-induced IFN-gamma production remained STAT4-dependent despite ectopic T-bet expression. Ectopic T-bet expression selectively induced expression of IL-12Rbeta2, but not IL-18Ralpha in wild-type and STAT1(-/-) T(H)2 cells, but did not extinguish expression of GATA-3 and T(H)2 cytokines. Finally, ectopic T-bet did not directly induce expression of endogenous T-bet independently of IFN-gamma or STAT1. Thus, T-bet is induced by IFN-gamma and STAT1 signaling during T cell activation. In addition, T-bet mediates STAT1- dependent processes of T(H)1 development, including the induction of IL-12Rbeta2.
引用
收藏
页码:549 / 557
页数:9
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