Yang Yu, Ochando Jordi, Yopp Adam, Bromberg Jonathan S, Ding Yaozhong
Department of Gene and Cell Medicine, The Recanati/Miller Transplantation Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.
J Immunol. 2005 Mar 1;174(5):2720-9. doi: 10.4049/jimmunol.174.5.2720.
The transcription factor c-Maf plays a critical and selective role in IL-4 gene transcription. Little is known about the mechanism that guides c-Maf regulation during early T cell activation. We report that IL-6 but not IL-4 or other cytokines, rapidly up-regulates c-Maf transcription, as early as 3 h after TCR activation in naive CD4(+) T cells. c-Maf induction requires both IL-6- and TCR-initiated signals, and is independent of IL-4/Stat6 signals. Cyclosporin A and FK506, which target calcineurin and thereby inhibit TCR-mediated Ca(2+) signal pathways, block IL-6-mediated c-Maf expression. We show that Stat3 binds the c-maf promoter in CD4 T cells after IL-6 stimulation, and also transactivates the c-maf promoter in reporter gene assays. IL-6 induces similar c-Maf expression in protein kinase Ctheta-deficient CD4(+) T cells. Furthermore, IL-6 enhances IL-4 gene expression very early after TCR activation in both wild-type and Stat6-deficient CD4(+) T cells. Our findings suggest that IL-6 plays a unique role in initiating c-Maf expression after TCR engagement, and may subsequently regulate early IL-4 production and Th2 commitment.
转录因子c-Maf在白细胞介素-4(IL-4)基因转录中发挥关键且具有选择性的作用。对于在早期T细胞激活过程中指导c-Maf调控的机制,我们所知甚少。我们报告称,在初始CD4(+) T细胞中,早在T细胞受体(TCR)激活后3小时,白细胞介素-6(IL-6)而非IL-4或其他细胞因子就能迅速上调c-Maf转录。c-Maf的诱导需要IL-6和TCR启动的信号,且独立于IL-4/信号转导子和转录激活子6(Stat6)信号。靶向钙调神经磷酸酶从而抑制TCR介导的钙离子(Ca(2+))信号通路的环孢素A和他克莫司(FK506),可阻断IL-6介导的c-Maf表达。我们发现,在IL-6刺激后,信号转导子和转录激活子3(Stat3)在CD4 T细胞中结合c-maf启动子,并且在报告基因检测中也能反式激活c-maf启动子。IL-6在蛋白激酶Cθ缺陷的CD4(+) T细胞中诱导相似的c-Maf表达。此外,在野生型和Stat6缺陷的CD4(+) T细胞中,IL-6在TCR激活后很早就增强了IL-4基因表达。我们的研究结果表明,IL-6在TCR结合后启动c-Maf表达中发挥独特作用,并可能随后调节早期IL-4产生和辅助性T细胞2(Th2)分化。