Hu Xiaoyu, Ivashkiv Lionel B
Arthritis and Tissue Degeneration Program, Hospital for Special Surgery, New York, NY 10021, USA.
Immunity. 2009 Oct 16;31(4):539-50. doi: 10.1016/j.immuni.2009.09.002.
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.
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的许多功能归因于STAT1直接介导的免疫效应基因诱导,但最近已经明确,关键的IFN-γ功能是通过对细胞对其他细胞因子和炎症因子反应的交叉调节来介导的。在这里,我们综述了IFN-γ和STAT1调节Toll样受体、炎症因子、组织破坏性细胞因子、抗炎细胞因子以及激活相反STAT的细胞因子信号传导的机制。这些信号传导机制揭示了IFN-γ如何调节巨噬细胞活化、炎症、组织重塑以及辅助性和调节性T细胞分化,以及Th1和Th17细胞反应如何在自身免疫性疾病中整合的见解。