Ouyang W, Jacobson N G, Bhattacharya D, Gorham J D, Fenoglio D, Sha W C, Murphy T L, Murphy K M
Department of Pathology and Center for Immunology, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.
Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3888-93. doi: 10.1073/pnas.96.7.3888.
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-gamma reporter by only 2-fold. Thus, determining the requirement for ERM in Th1 development likely will require gene targeting.
白细胞介素12(IL-12)诱导的辅助性T细胞1(Th1)发育需要Stat4激活。然而,抗原激活的Th1细胞可独立于IL-12和Stat4激活产生干扰素γ(IFN-γ)。因此,在分化的Th1细胞中,受IL-12和Stat4调控的因子可能参与IFN-γ的产生。通过消减克隆,我们鉴定出Ets转录因子ERM是Th1特异性的、IL-12诱导的基因。ERM的IL-12诱导在野生型和Stat1缺陷型T细胞中发生,但在Stat4缺陷型T细胞中未发生,提示ERM是Stat4可诱导的。ERM的逆转录病毒表达不能恢复Stat4缺陷型T细胞中的IFN-γ产生,但可增强Stat4杂合型T细胞中的IFN-γ表达。Ets因子通常通过与其他转录因子的协同相互作用来调节转录,并且据报道ERM可与c-Jun协同作用。然而,在没有其他转录因子的情况下,ERM仅使IFN-γ报告基因的表达增加2倍。因此,确定ERM在Th1发育中的需求可能需要基因打靶。