Department of Biochemistry and Molecular Biology, The Fourth Military Medical University, Xi'an, 710032, China.
Semin Immunopathol. 2010 Jun;32(2):149-56. doi: 10.1007/s00281-009-0192-1. Epub 2010 Jan 28.
Regulatory T cells (Tregs) play a critical role in maintaining immune tolerance to self-antigens, whose development and activation is controlled by the master regulator and transcription factor Foxp3. Foxp3 acts as transcription repressor and exerts its suppressing function via directly associating with and inhibiting the function of other transcriptional regulators. The gene transcription of Foxp3 is regulated by diverse mechanisms at the cellular and molecular levels including the pleiotropic cytokine transforming growth factor-beta (TGF-beta). Itch is an E3 ubiquitin ligase whose deficiency is linked to excessive immune responses, abnormal T helper cell differentiation, and failed T cell anergy induction. Recent evidence indicates that Itch is involved in TGF-beta-induced Foxp3 expression and Treg-regulated airway inflammation, thus identifying a ubiquitin-dependent pathway in modulating Tregs.
调节性 T 细胞(Tregs)在维持对自身抗原的免疫耐受方面发挥着关键作用,其发育和激活受主调控因子和转录因子 Foxp3 的控制。Foxp3 作为转录抑制因子,通过直接与其他转录调控因子结合并抑制其功能来发挥抑制作用。Foxp3 的基因转录受细胞和分子水平上多种机制的调节,包括多效性细胞因子转化生长因子-β(TGF-β)。Itch 是一种 E3 泛素连接酶,其缺乏与过度免疫反应、异常 T 辅助细胞分化和 T 细胞无能诱导失败有关。最近的证据表明,Itch 参与 TGF-β诱导的 Foxp3 表达和 Treg 调节的气道炎症,从而确定了调节 Tregs 的泛素依赖性途径。