Cross-regulation of Signaling Pathways by Interferon-γ: Implications for Immune Responses and Autoimmune Diseases

被引:703
作者
Hu, Xiaoyu [1 ,2 ]
Ivashkiv, Lionel B. [1 ,2 ,3 ]
机构
[1] Hosp Special Surg, Arthrit & Tissue Degenerat Program, New York, NY 10021 USA
[2] Weill Cornell Med Coll, Dept Med, New York, NY 10021 USA
[3] Weill Cornell Grad Sch Med Sci, Grad Program Immunol & Microbial Pathogenesis, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
COLLAGEN-INDUCED ARTHRITIS; COLONY-STIMULATING FACTOR; RECEPTOR-DEFICIENT MICE; NECROSIS-FACTOR-ALPHA; GENE-SPECIFIC CONTROL; TOLL-LIKE RECEPTOR; NF-KAPPA-B; IFN-GAMMA; T-CELLS; MACROPHAGE ACTIVATION;
D O I
10.1016/j.immuni.2009.09.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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.
引用
收藏
页码:539 / 550
页数:12
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