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The AGC kinase serum- and glucocorticoid-regulated kinase 1 (SGK1) regulates TH1 and TH2 differentiation downstream of mTORC2

机译:AGC激酶血清和糖皮质激素调节激酶1(SGK1)调节mTORC2下游的TH1和TH2分化

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摘要

Serum- and glucocorticoid-regulated kinase 1 (SGK1) is an AGC kinase that regulates membrane sodium channel expression in renal tubular cells in an mTORC2-dependent manner. We hypothesized that SGK1 might represent a novel mTORC2-dependent regulator of T cell differentiation and function. Here we demonstrate that upon activation by mTORC2, SGK1 promoted TH2 differentiation by negatively regulating the NEDD4-2 E3 ligase-mediated destruction of transcription factor JunB. Simultaneously, SGK1 repressed the production of interferon-γ (IFN-γ) by controlling the expression of the long isoform of transcription factor TCF-1. Consistent with these findings, mice with a selective deletion of SGK1 in T cells were resistant to experimentally induced asthma, generated robust amounts of IFN-γ in response to viral infections and more readily rejected tumors.
机译:血清和糖皮质激素调节激酶1(SGK1)是一种AGC激酶,它以依赖mTORC2的方式调节肾小管细胞膜钠通道的表达。我们假设SGK1可能代表T细胞分化和功能的新型mTORC2依赖调节剂。在这里,我们证明了通过mTORC2激活后,SGK1通过负调节NEDD4-2 E3连接酶介导的转录因子JunB的破坏来促进TH2分化。同时,SGK1通过控制转录因子TCF-1的长异构体的表达来抑制干扰素-γ(IFN-γ)的产生。与这些发现一致的是,在T细胞中选择性删除SGK1的小鼠对实验诱导的哮喘有抵抗力,对病毒感染产生了强大量的IFN-γ,更容易排斥肿瘤。

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