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抑素 1 通过损害 RIG-I 样受体信号通路促进病毒复制。

Prohibitin1 facilitates viral replication by impairing the RIG-I-like receptor signaling pathway.

机构信息

National Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University , Wuhan, Hubei, China.

Key Laboratory of Preventive Veterinary Medicine in Hubei Province, The Cooperative Innovation Center for Sustainable Pig Production , Wuhan, Hubei, China.

出版信息

J Virol. 2023 Oct 31;97(10):e0092623. doi: 10.1128/jvi.00926-23. Epub 2023 Sep 27.

Abstract

Type I interferon (IFN-I), produced by the innate immune system, plays an essential role in host antiviral responses. Proper regulation of IFN-I production is required for the host to balance immune responses and prevent superfluous inflammation. IFN regulatory factor 3 (IRF3) and subsequent sensors are activated by RNA virus infection to induce IFN-I production. Therefore, proper regulation of IRF3 serves as an important way to control innate immunity and viral replication. Here, we first identified Prohibitin1 (PHB1) as a negative regulator of host IFN-I innate immune responses. Mechanistically, PHB1 inhibited the nucleus import of IRF3 by impairing its binding with importin subunit alpha-1 and importin subunit alpha-5. Our study demonstrates the mechanism by which PHB1 facilitates the replication of multiple RNA viruses and provides insights into the negative regulation of host immune responses.

摘要

I 型干扰素(IFN-I)由先天免疫系统产生,在宿主抗病毒反应中发挥重要作用。为了使宿主平衡免疫反应并防止过度炎症,需要对 IFN-I 的产生进行适当的调节。RNA 病毒感染激活 IFN 调节因子 3(IRF3)和随后的传感器,诱导 IFN-I 的产生。因此,适当调节 IRF3 是控制先天免疫和病毒复制的重要途径。在这里,我们首次鉴定出 PHB1 是宿主 IFN-I 先天免疫反应的负调控因子。从机制上讲,PHB1 通过损害其与导入蛋白亚基α-1 和导入蛋白亚基α-5 的结合,抑制了 IRF3 的核内导入。我们的研究阐明了 PHB1 促进多种 RNA 病毒复制的机制,并为宿主免疫反应的负调控提供了新的见解。

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