内部收益率3
坦克结合激酶1
干扰素调节因子
信号转导衔接蛋白
细胞生物学
激酶
信号转导
IκB激酶
转录因子
生物
激活剂(遗传学)
先天免疫系统
蛋白激酶A
NF-κB
免疫学
免疫系统
受体
遗传学
MAP激酶激酶激酶
基因
作者
Mariya Al Hamrashdi,Gareth Brady
标识
DOI:10.1016/j.bcp.2022.115026
摘要
The interferon regulatory factor (IRF) family of transcription factors play a vital role in the human innate antiviral immune responses with production of interferons (IFNs) as a hallmark outcome of activation. In recent years, IRF3 has been considered a principal early regulator of type I IFNs (TI-IFNs) directly downstream of intracellular virus sensing. Despite decades of research on IRF-activating pathways, many questions remain on the regulation of IRF3 activation. The kinases IκB kinase epsilon (IKKε) and TANK-binding kinase-1 (TBK1) and the scaffold proteins TRAF family member-associated NF-kappa-B activator (TANK), NF-kappa-B-activating kinase-associated protein 1 (NAP1) and TANK-binding kinase 1-binding protein 1 (TBKBP1)/similar to NAP1 TBK1 adaptor (SINTBAD) are believed to be core components of an IRF3-activation complex yet their contextual involvement and complex composition are still unclear. This review will give an overview of antiviral signaling pathways leading to the activation of IRF3 and discuss recent developments in our understanding of its proximal regulation.
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