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前沿:转录因子 Kruppel 样因子 4 通过不依赖于 RORγt 的方式调控 Th17 细胞的分化。

Cutting edge: The transcription factor Kruppel-like factor 4 regulates the differentiation of Th17 cells independently of RORγt.

机构信息

Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

J Immunol. 2010 Dec 15;185(12):7161-4. doi: 10.4049/jimmunol.1002750. Epub 2010 Nov 12.

Abstract

Th17 cells play a significant role in inflammatory and autoimmune responses. Although a number of molecular pathways that contribute to the lineage differentiation of T cells have been discovered, the mechanisms by which lineage commitment occurs are not fully understood. Transcription factors play a key role in driving T cells toward specific lineages. We have identified a role for the transcription factor Kruppel-like factor (KLF) 4 in the development of IL-17-producing CD4(+) T cells. KLF4 was required for the production of IL-17, and further, chromatin immunoprecipitation analysis demonstrated binding of KLF4 to the IL-17 promoter, indicating a direct effect on the regulation of IL-17. Further, KLF4-deficient T cells upregulated expression of retinoic acid-related orphan receptor γt similar to wild-type during the polarization process toward Th17, suggesting that these two transcription factors are regulated independently.

摘要

Th17 细胞在炎症和自身免疫反应中发挥重要作用。尽管已经发现了许多有助于 T 细胞谱系分化的分子途径,但谱系分化发生的机制尚不完全清楚。转录因子在促使 T 细胞向特定谱系分化方面发挥着关键作用。我们已经确定转录因子 Kruppel 样因子(KLF)4 在产生白细胞介素-17(IL-17)的 CD4+T 细胞的发育中起作用。KLF4 对于 IL-17 的产生是必需的,进一步的染色质免疫沉淀分析表明 KLF4 与 IL-17 启动子结合,表明其对 IL-17 的调节具有直接作用。此外,KLF4 缺陷型 T 细胞在向 Th17 极化过程中上调维甲酸相关孤儿受体 γt 的表达,类似于野生型,这表明这两个转录因子是独立调控的。

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