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鱼泛素特异性蛋白酶 8(USP8)通过自噬溶酶体依赖的 IRF7 降解来抑制 IFN 的产生。

Fish ubiquitin-specific protease 8 (USP8) inhibits IFN production through autophagy-lysosomal dependent degradation of IRF7.

机构信息

College of Fisheries and Life Science, Dalian Ocean University, Dalian, China; Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China.

Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China; University of Chinese Academy of Sciences, Beijing, China.

出版信息

Dev Comp Immunol. 2024 Jul;156:105181. doi: 10.1016/j.dci.2024.105181. Epub 2024 Apr 16.

Abstract

Interferon regulatory factor 7 (IRF7) is considered the master regulator of virus-induced interferon (IFN) production. However, to avoid an autoimmune response, the expression of IRF7 must be tightly controlled. In this study, we report that zebrafish ubiquitin-specific protease 8 (USP8) promotes IRF7 degradation through an autophagy-lysosome-dependent pathway to inhibit IFN production. First, zebrafish usp8 is induced upon spring viremia of carp virus (SVCV) infection and polyinosinic/polycytidylic acid (poly I:C) stimulation. Second, overexpression of USP8 suppresses SVCV or poly I:C-mediated IFN expression. Mechanistically, USP8 interacts with IRF7 and promotes its degradation via an autophagy-lysosome-dependent pathway. Finally, USP8 significantly suppresses cellular antiviral responses and enhances SVCV proliferation. In summary, our discoveries offer a perspective on the role of zebrafish USP8 and provide additional understanding of the regulation of IRF7 in host antiviral immune response.

摘要

干扰素调节因子 7 (IRF7) 被认为是病毒诱导干扰素 (IFN) 产生的主要调节因子。然而,为了避免自身免疫反应,IRF7 的表达必须受到严格控制。在这项研究中,我们报告说,斑马鱼泛素特异性蛋白酶 8 (USP8) 通过自噬溶酶体依赖性途径促进 IRF7 降解,从而抑制 IFN 的产生。首先,在鲤鱼病毒 (SVCV) 感染和多聚肌苷酸/多聚胞苷酸 (poly I:C) 刺激下,斑马鱼 usp8 被诱导。其次,USP8 的过表达抑制 SVCV 或 poly I:C 介导的 IFN 表达。在机制上,USP8 与 IRF7 相互作用,并通过自噬溶酶体依赖性途径促进其降解。最后,USP8 显著抑制细胞抗病毒反应并增强 SVCV 的增殖。总之,我们的发现为斑马鱼 USP8 的作用提供了一个视角,并为宿主抗病毒免疫反应中 IRF7 的调节提供了更多的理解。

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