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首页> 外文期刊>Nature immunology >Runx-CBFbeta complexes control expression of the transcription factor Foxp3 in regulatory T cells.
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Runx-CBFbeta complexes control expression of the transcription factor Foxp3 in regulatory T cells.

机译:Runx-CBFbeta复合物控制调节性T细胞中转录因子Foxp3的表达。

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The transcription factor Foxp3 has an indispensable role in establishing stable transcriptional and functional programs of regulatory T cells (T(reg) cells). Loss of Foxp3 expression in mature T(reg) cells results in a failure of suppressor function, yet the molecular mechanisms that ensure steady, heritable Foxp3 expression in the T(reg) cell lineage remain unknown. Using T(reg) cell-specific gene targeting, we found that complexes of the transcription factors Runx and CBFbeta were required for maintenance of Foxp3 mRNA and protein expression in T(reg) cells. Consequently, mice lacking CBFbetab exclusively in the T(reg) cell lineage had a moderate lymphoproliferative syndrome. Thus, Runx-CBFbeta complexes maintain stable high expression of Foxp3 and serve as an essential determinant of T(reg) cell lineage stability.
机译:转录因子Foxp3在建立稳定的调节性T细胞(T(reg)细胞)的转录和功能程序中起着不可或缺的作用。成熟的T(reg)细胞中Foxp3表达的丧失导致抑制功能的失败,但是确保T(reg)细胞谱系中稳定,可遗传的Foxp3表达的分子机制仍然未知。使用T(reg)细胞特异性基因靶向,我们发现转录因子Runx和CBFbeta的复合物是维持T(reg)细胞中Foxp3 mRNA和蛋白表达所必需的。因此,仅在T(reg)细胞谱系中缺乏CBFbetab的小鼠患有中度淋巴细胞增生综合征。因此,Runx-CBFbeta复合物保持Foxp3的稳定高表达,并作为T(reg)细胞谱系稳定性的重要决定因素。

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