A novel transcription factor, T-bet, directs Th1 lineage commitment

被引:2867
作者
Szabo, SJ
Kim, ST
Costa, GL
Zhang, XK
Fathman, CG
Glimcher, LH
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Stanford Univ, Sch Med, Div Rheumatol & Immunol, Stanford, CA 94305 USA
[4] Med Univ S Carolina, Div Rheumatol & Immunol, Charleston, SC 29425 USA
关键词
D O I
10.1016/S0092-8674(00)80702-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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, IFN gamma. T-bet expression correlates with IFN gamma expression in Th1 and NK cells. Ectopic expression of T-bet both transactivates the IFN gamma gene and induces endogenous IFN gamma 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 IFN gamma 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.
引用
收藏
页码:655 / 669
页数:15
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