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转录因子 Foxp1 调节 Foxp3 染色质结合并协调调节性 T 细胞功能。

Transcription factor Foxp1 regulates Foxp3 chromatin binding and coordinates regulatory T cell function.

机构信息

Howard Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Nat Immunol. 2019 Feb;20(2):232-242. doi: 10.1038/s41590-018-0291-z. Epub 2019 Jan 14.

Abstract

Regulatory T cells (T cells), whose differentiation and function are controlled by transcription factor Foxp3, express the closely related family member Foxp1. Here we explored Foxp1 function in T cells. We found that a large number of Foxp3-bound genomic sites in T cells were occupied by Foxp1 in both T cells and conventional T cells (T cells). In T cells, Foxp1 markedly increased Foxp3 binding to these sites. Foxp1 deficiency in T cells resulted in their impaired function and competitive fitness, associated with markedly reduced CD25 expression and interleukin-2 (IL-2) responsiveness, diminished CTLA-4 expression and increased SATB1 expression. The characteristic expression patterns of CD25, Foxp3 and CTLA-4 in T cells were fully or partially rescued by strong IL-2 signaling. Our studies suggest that Foxp1 serves an essential non-redundant function in T cells by enforcing Foxp3-mediated regulation of gene expression and enabling efficient IL-2 signaling in these cells.

摘要

调节性 T 细胞(Tregs),其分化和功能受转录因子 Foxp3 控制,表达密切相关的家族成员 Foxp1。在这里,我们研究了 Foxp1 在 T 细胞中的功能。我们发现,在 T 细胞和传统 T 细胞(Tconv)中,大量 Foxp3 结合的基因组位点被 Foxp1 占据。在 T 细胞中,Foxp1 显著增加了 Foxp3 对这些位点的结合。Foxp1 在 T 细胞中的缺失导致其功能受损和竞争适应性降低,伴随着 CD25 表达和白细胞介素 2(IL-2)反应性显著降低,CTLA-4 表达减少和 SATB1 表达增加。T 细胞中 CD25、Foxp3 和 CTLA-4 的特征表达模式通过强 IL-2 信号得到完全或部分挽救。我们的研究表明,Foxp1 通过强制 Foxp3 介导的基因表达调控并使这些细胞中有效的 IL-2 信号传导,在 T 细胞中发挥不可或缺的非冗余功能。

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