首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >IL-6-dependent and -independent pathways in the development of interleukin 17-producing T helper cells
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IL-6-dependent and -independent pathways in the development of interleukin 17-producing T helper cells

机译:IL-6依赖性和非依赖性途径在产生白介素17的T辅助细胞发育中的作用

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CD4~+ T cells producing IL-17 [T helper (Th)17], as distinct from Th1 or Th2 cells, have recently been shown to be associated with autoimmunity, but it is not entirely clear how Th17 cells are generated from naieve T cells. We demonstrate here that IL-6, but not TNF-α or IL-1β, can, in combination with TGF-β, induce Th17 cell generation from naieve T cells and inhibit TGF-β-induced Foxp3 expression. Moreover, conditioned medium from lipopolysaccharide-stimulated bone marrow-derived dendritic cells (DCCM) can induce IL-17 production in naieve T cells. Interestingly, IL-17 was produced by DCCM even with the addition of anti-gp130 antibody or DCCM from IL-6 KO mice. The combination of IL-6 and TGF-β could maintain activation of signal transducer and activator of transcription (Stat)3, but not of Stat1. IL-27 or IFN-γ suppressed the induction of Th17 cells by TGF-β plus IL-6 and maintained Stat1 activation under these conditions. In contrast, both Stat1 and Stat3 remained to be activated in naieve T cells cultured with DCCM. These findings represent a different basis for Th17 differentiation from naieve T cells.
机译:与Th1或Th2细胞不同的是,产生IL-17 [T辅助(Th)17]的CD4〜+ T细胞最近被证明与自身免疫有关,但尚不清楚如何从幼稚T产生Th17细胞细胞。我们在这里证明IL-6,而不是TNF-α或IL-1β,可以与TGF-β结合,从幼稚T细胞诱导Th17细胞生成并抑制TGF-β诱导的Foxp3表达。此外,来自脂多糖刺激的骨髓树突状细胞(DCCM)的条件培养基可以诱导幼稚T细胞中IL-17的产生。有趣的是,即使添加了来自IL-6 KO小鼠的抗gp130抗体或DCCM,DCCM也会产生IL-17。 IL-6和TGF-β的组合可以维持信号转导子和转录激活子(Stat)3的激活,但不能维持Stat1的激活。在这些条件下,IL-27或IFN-γ抑制了TGF-β加IL-6对Th17细胞的诱导,并维持了Stat1激活。相反,在用DCCM培养的幼稚T细胞中,Stat1和Stat3仍然被激活。这些发现代表从原始T细胞分化Th17的不同基础。

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