Department of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Nat Immunol. 2012 Jul 1;13(8):778-86. doi: 10.1038/ni.2362.
Sox4 is a transcription factor that regulates various developmental processes. Here we show that Sox4 was induced by TGF-β and negatively regulated the transcription factor GATA-3, the master regulator of function of T helper type 2 (T(H)2) cells, by two distinct mechanisms. First, Sox4 bound directly to GATA-3, preventing its binding to GATA-3 consensus DNA sequences. Second, Sox4 bound to the promoter region of the gene encoding interleukin 5 (IL-5), a T(H)2 cytokine, and prevented binding of GATA-3 to this promoter. T(H)2 cell-driven airway inflammation was modulated by alterations in Sox4 expression. Thus, Sox4 acted as a downstream target of TGF-β to inhibit GATA-3 function, T(H)2 differentiation and T(H)2 cell-mediated inflammation.
Sox4 是一种转录因子,可调节各种发育过程。在这里,我们表明 Sox4 被 TGF-β诱导,并通过两种不同的机制负调控转录因子 GATA-3,GATA-3 是 T 辅助细胞 2(T(H)2)细胞功能的主要调节因子。首先,Sox4 直接与 GATA-3 结合,阻止其与 GATA-3 共有 DNA 序列结合。其次,Sox4 与编码白细胞介素 5(IL-5)的基因的启动子区域结合,阻止 GATA-3 与该启动子结合。IL-5 是一种 T(H)2 细胞因子。通过改变 Sox4 的表达来调节 T(H)2 细胞驱动的气道炎症。因此,Sox4 作为 TGF-β 的下游靶标,抑制 GATA-3 功能、T(H)2 分化和 T(H)2 细胞介导的炎症。