NFATc2 and T-bet contribute to T-helper-cell-subset-specific regulation of IL-21 expression

被引:70
作者
Mehta, DS
Wurster, AL
Weinmann, AS
Grusby, MJ
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
关键词
cytokine; promoter; transcription factor;
D O I
10.1073/pnas.0409512102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
T helper (Th) 2 cells selectively express IL-21 in addition to the classic Th2 cytokines IL-4, IL-5, and IL-13. In contrast to these clustered Th2 cell cytokine genes, the IL-21 gene resides on a different chromosome and is not coordinately regulated by the same locus control region that directs the expression of other Th2 cytokines. We demonstrate that the proximal promoter of IL-21 controls its Th-cell-subset-specific expression through the action of NFATc2 and T-bet. Whereas NFATc2 directly binds to and activates transcription of the IL-21 promoter in Th2 cells, T-bet represses IL-21 transcription by inhibiting the binding of NFATc2 to the promoter in Th1 cells. These data suggest that there are multiple mechanisms by which Th-cell-subset-specific cytokine genes are regulated.
引用
收藏
页码:2016 / 2021
页数:6
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