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首页> 外文期刊>Immunity >Interleukin-17C promotes Th17 cell responses and autoimmune disease via interleukin-17 receptor E.
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Interleukin-17C promotes Th17 cell responses and autoimmune disease via interleukin-17 receptor E.

机译:白介素17C通过白介素17受体E促进Th17细胞反应和自身免疫性疾病。

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摘要

Although several interleukin-17 (IL-17) family members and their receptors have been recently appreciated as important regulators in inflammatory diseases, the function of other IL-17 cytokines and IL-17 receptor-like molecules is unclear. Here we show that an IL-17 cytokine family member, IL-17C, was induced in a Th17 cell-dependent autoimmune disease and was required for its pathogenesis. IL-17C bound to IL-17RE, a member of IL-17 receptor family whose full-length isoform was selectively expressed in Th17 cells and signaled via an IL-17RA-RE receptor complex and the downstream adaptor Act1. IL-17C-IL-17RE induced the expression of a nuclear IkappaB family member, IkappaBzeta, in Th17 cells to potentiate the Th17 cell response. Thus, our work has identified a cytokine-receptor pair with important function in regulating proinflammatory responses. This pathway may be targeted to treat autoimmune diseases.
机译:尽管最近已认识到一些白介素17(IL-17)家族成员及其受体是炎性疾病中的重要调节剂,但其他IL-17细胞因子和类IL-17受体分子的功能尚不清楚。在这里,我们显示IL-17细胞因子家族成员IL-17C在Th17细胞依赖性自身免疫性疾病中被诱导,并且是其发病机理所必需的。 IL-17C与IL-17RE结合,IL-17RE是IL-17受体家族的成员,其全长同工型在Th17细胞中选择性表达,并通过IL-17RA-RE受体复合物和下游衔接子Act1发出信号。 IL-17C-IL-17RE诱导Th17细胞中IkappaB家族核成员IkappaBzeta的表达,以增强Th17细胞的应答。因此,我们的工作已经确定了在调节促炎反应中具有重要功能的细胞因子受体对。该途径可以靶向治疗自身免疫疾病。

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