Szabo S J, Kim S T, Costa G L, Zhang X, Fathman C G, Glimcher L H
Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Cell. 2000 Mar 17;100(6):655-69. doi: 10.1016/s0092-8674(00)80702-3.
Naive T helper cells differentiate into two subsets, Th1 and Th2, each with distinct functions and cytokine profiles. Here, we report the isolation of T-bet, a Th1-specific T box transcription factor that controls the expression of the hallmark Th1 cytokine, IFNgamma. T-bet expression correlates with IFNgamma expression in Th1 and NK cells. Ectopic expression of T-bet both transactivates the IFNgamma gene and induces endogenous IFNgamma production. Remarkably, retroviral gene transduction of T-bet into polarized Th2 and Tc2 primary T cells redirects them into Th1 and Tc1 cells, respectively, as evidenced by the simultaneous induction of IFNgamma and repression of IL-4 and IL-5. Thus, T-bet initiates Th1 lineage development from naive Thp cells both by activating Th1 genetic programs and by repressing the opposing Th2 programs.
初始辅助性T细胞分化为两个亚群,即Th1和Th2,每个亚群都有独特的功能和细胞因子谱。在此,我们报告了T-bet的分离,T-bet是一种Th1特异性的T盒转录因子,它控制着标志性Th1细胞因子IFNγ的表达。T-bet的表达与Th1细胞和自然杀伤细胞中IFNγ的表达相关。T-bet的异位表达既能反式激活IFNγ基因,又能诱导内源性IFNγ的产生。值得注意的是,将T-bet通过逆转录病毒基因转导到极化的Th2和Tc2原代T细胞中,可分别将它们重定向为Th1和Tc1细胞,这可通过IFNγ的同时诱导以及IL-4和IL-5的抑制得以证明。因此,T-bet通过激活Th1遗传程序和抑制相反的Th2程序,启动了从初始Thp细胞开始的Th1谱系发育。