首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >NFATc2 and T-bet contribute to T-helper-cell-subset-specific regulation of IL-21 expression.
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NFATc2 and T-bet contribute to T-helper-cell-subset-specific regulation of IL-21 expression.

机译:NFATc2和T-bet有助于IL-21表达的T辅助细胞亚群特异性调节。

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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.
机译:除经典的Th2细胞因子IL-4,IL-5和IL-13外,T辅助(Th)2细胞还选择性表达IL-21。与这些簇集的Th2细胞因子基因相反,IL-21基因位于不同的染色体上,并且不受指导其他Th2细胞因子表达的相同基因座控制区的协调调控。我们证明IL-21的近端启动子通过NFATc2和T-bet的作用控制其Th细胞亚群的特异性表达。 NFATc2直接与Th2细胞中的IL-21启动子结合并激活其转录,而T-bet通过抑制NFATc2与Th1细胞中的启动子结合来抑制IL-21转录。这些数据表明存在多种调节Th细胞亚群特异性细胞因子基因的机制。

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