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

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials 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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引用次数: 0

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

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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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