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

IF 2.4 3区 农林科学 Q1 FISHERIES Developmental and comparative immunology Pub Date : 2024-04-16 DOI:10.1016/j.dci.2024.105181
Chu-Jing Zhou , Can Zhang , Long-Feng Lu , Shun Li
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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.

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鱼类泛素特异性蛋白酶 8 (USP8) 通过自噬-溶酶体依赖性降解 IRF7 抑制 IFN 的产生
干扰素调节因子 7(IRF7)被认为是病毒诱导干扰素(IFN)产生的主调节因子。然而,为了避免自身免疫反应,必须严格控制 IRF7 的表达。在这项研究中,我们报告了斑马鱼泛素特异性蛋白酶8(USP8)通过自噬-溶酶体依赖途径促进IRF7降解,从而抑制IFN的产生。首先,鲤鱼春季病毒(SVCV)感染和多聚肌苷酸/多聚胞苷酸(poly I:C)刺激会诱导斑马鱼 usp8。其次,过表达 USP8 可抑制 SVCV 或 poly I:C 介导的 IFN 表达。从机理上讲,USP8 与 IRF7 相互作用,并通过自噬-溶酶体依赖途径促进其降解。最后,USP8 会明显抑制细胞的抗病毒反应,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,并使人们对 IRF7 在宿主抗病毒免疫反应中的调控有了更多的了解。
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来源期刊
CiteScore
6.20
自引率
6.90%
发文量
206
审稿时长
49 days
期刊介绍: Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.
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