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Cross-regulation of signaling pathways by interferon-gamma: implications for immune responses and autoimmune diseases.

机译:干扰素-γ对信号通路的交叉调节:对免疫反应和自身免疫性疾病的影响。

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摘要

Interferon-gamma (IFN-gamma) is an important mediator of immunity and inflammation that utilizes the JAK-STAT signaling pathway to activate the STAT1 transcription factor. Many functions of IFN-gamma have been ascribed to direct STAT1-mediated induction of immune effector genes, but recently it has become clear that key IFN-gamma functions are mediated by cross-regulation of cellular responses to other cytokines and inflammatory factors. Here, we review mechanisms by which IFN-gamma and STAT1 regulate signaling by Toll-like receptors, inflammatory factors, tissue-destructive cytokines, anti-inflammatory cytokines, and cytokines that activate opposing STATs. These signaling mechanisms reveal insights about how IFN-gamma regulates macrophage activation, inflammation, tissue remodeling, and helper and regulatory T cell differentiation and how Th1 and Th17 cell responses are integrated in autoimmune diseases.
机译:干扰素-γ(IFN-γ)是免疫和炎症的重要介质,它利用JAK-STAT信号通路激活STAT1转录因子。 IFN-γ的许多功能已被归因于直接STAT1介导的免疫效应基因的诱导,但是最近变得很清楚,关键的IFN-γ功能是由细胞对其他细胞因子和炎症因子的交叉调节所介导的。在这里,我们综述了IFN-γ和STAT1通过Toll样受体,炎症因子,组织破坏性细胞因子,抗炎细胞因子和激活相对STAT的细胞因子调节信号传导的机制。这些信号传导机制揭示了有关IFN-γ如何调节巨噬细胞活化,炎症,组织重塑以及辅助和调节性T细胞分化以及Th1和Th17细胞反应如何整合到自身免疫疾病中的见解。

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