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人类先天免疫途径中 NF-κB 和 IRF 家族激活的信号转导分支。

Bifurcation of signalling in human innate immune pathways to NF-kB and IRF family activation.

机构信息

Trinity Translational Medicine Institute, St James' Campus, Trinity College Dublin, D08 W9RT Dublin, Ireland.

出版信息

Biochem Pharmacol. 2022 Nov;205:115246. doi: 10.1016/j.bcp.2022.115246. Epub 2022 Sep 8.

Abstract

The human innate immune response can be activated through a wide range of stimuli. This multi-faceted system can be triggered by a range of immunostimulants including pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs). These stimuli drive intracellular signalling pathways that branch off downstream to activate several distinct transcription factors. The two most impactful of which in innate immune outcomes are the NF-κB and the IRF family members. Both transcription factor families play defining roles in driving inflammation as well as the antiviral response. Pathways leading to their simultaneous activation share common upstream components but eventually distinct regulators which directly facilitate their activation. This review will discuss the current state of knowledge about what is known about how these pathways bifurcate to activate NF-κB and IRF family members.

摘要

人体先天免疫反应可以通过多种刺激激活。这个多方面的系统可以被一系列免疫刺激物触发,包括病原体相关分子模式(PAMPs)和损伤相关分子模式(DAMPs)。这些刺激物驱动细胞内信号通路分支,激活几个不同的转录因子。其中对先天免疫结果影响最大的是 NF-κB 和 IRF 家族成员。这两个转录因子家族在驱动炎症和抗病毒反应方面都起着决定性的作用。导致它们同时激活的途径具有共同的上游成分,但最终有不同的调节剂直接促进它们的激活。这篇综述将讨论目前已知的关于这些途径如何分叉激活 NF-κB 和 IRF 家族成员的知识状况。

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