Howard Hughes Medical Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nat Immunol. 2019 Feb;20(2):232-242. doi: 10.1038/s41590-018-0291-z. Epub 2019 Jan 14.
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.
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。