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人类抗病毒信号通路中IRF3激活的调控

Regulation of IRF3 activation in human antiviral signaling pathways.

作者信息

Al Hamrashdi Mariya, Brady Gareth

机构信息

Trinity Translational Medicine Institute, Trinity College Dublin, St. James' Hospital Campus, Dublin, Ireland.

出版信息

Biochem Pharmacol. 2022 Jun;200:115026. doi: 10.1016/j.bcp.2022.115026. Epub 2022 Mar 31.

Abstract

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.

摘要

干扰素调节因子(IRF)转录因子家族在人类先天性抗病毒免疫反应中起着至关重要的作用,其标志性结果是产生干扰素(IFN)。近年来,IRF3被认为是I型干扰素(TI-IFN)的主要早期调节因子,直接位于细胞内病毒感知的下游。尽管对IRF激活途径进行了数十年的研究,但关于IRF3激活的调控仍存在许多问题。激酶IκB激酶ε(IKKε)和TANK结合激酶1(TBK1)以及支架蛋白TRAF家族成员相关的NF-κB激活剂(TANK)、NF-κB激活激酶相关蛋白1(NAP1)和TANK结合激酶1结合蛋白1(TBKBP1)/类似于NAP1的TBK1衔接子(SINTBAD)被认为是IRF3激活复合物的核心成分,但其具体参与情况和复合物组成仍不清楚。本综述将概述导致IRF3激活的抗病毒信号通路,并讨论我们对其近端调控理解的最新进展。

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