贾纳斯激酶
STAT蛋白
生物
斯达
JAK-STAT信号通路
细胞生物学
自身免疫
干扰素
抄写(语言学)
车站3
信号转导
转录因子
获得性免疫系统
免疫学
免疫系统
STAT1
Janus激酶1
信号
先天免疫系统
基因
遗传学
酪氨酸激酶
语言学
哲学
作者
Lionel B. Ivashkiv,Laura T. Donlin
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2013-12-23
卷期号:14 (1): 36-49
被引量:2712
摘要
This Review describes the intricate signalling and epigenetic mechanisms that regulate cellular responses to type I interferons. The authors also discuss how persistent interferon-mediated signalling can have detrimental outcomes in autoimmune disease and chronic infections. Type I interferons (IFNs) activate intracellular antimicrobial programmes and influence the development of innate and adaptive immune responses. Canonical type I IFN signalling activates the Janus kinase (JAK)–signal transducer and activator of transcription (STAT) pathway, leading to transcription of IFN-stimulated genes (ISGs). Host, pathogen and environmental factors regulate the responses of cells to this signalling pathway and thus calibrate host defences while limiting tissue damage and preventing autoimmunity. Here, we summarize the signalling and epigenetic mechanisms that regulate type I IFN-induced STAT activation and ISG transcription and translation. These regulatory mechanisms determine the biological outcomes of type I IFN responses and whether pathogens are cleared effectively or chronic infection or autoimmune disease ensues.
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