An Integrated View of Deubiquitinating Enzymes Involved in Type I Interferon Signaling, Host Defense and Antiviral Activities

被引:6
|
作者
Qian, Guanghui [1 ]
Zhu, Liyan [2 ]
Li, Gen [1 ]
Liu, Ying [1 ]
Zhang, Zimu [1 ]
Pan, Jian [1 ]
Lv, Haitao [1 ]
机构
[1] Soochow Univ, Childrens Hosp, Inst Pediat Res, Suzhou, Peoples R China
[2] Soochow Univ, Med Coll, Dept Expt Ctr, Suzhou, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
基金
中国国家自然科学基金;
关键词
deubiquitinating enzymes; type I IFN signaling; ubiquitin; virus infection; innate immunity; NF-KAPPA-B; E3 UBIQUITIN LIGASE; IMMUNE PATTERN-RECOGNITION; IFN-BETA PRODUCTION; RIG-I; LINEAR POLYUBIQUITIN; NEGATIVE REGULATION; INNATE IMMUNITY; ACTIVATION; USP18;
D O I
10.3389/fimmu.2021.742542
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Viral infectious diseases pose a great challenge to human health around the world. Type I interferons (IFN-Is) function as the first line of host defense and thus play critical roles during virus infection by mediating the transcriptional induction of hundreds of genes. Nevertheless, overactive cytokine immune responses also cause autoimmune diseases, and thus, tight regulation of the innate immune response is needed to achieve viral clearance without causing excessive immune responses. Emerging studies have recently uncovered that the ubiquitin system, particularly deubiquitinating enzymes (DUBs), plays a critical role in regulating innate immune responses. In this review, we highlight recent advances on the diverse mechanisms of human DUBs implicated in IFN-I signaling. These DUBs function dynamically to calibrate host defenses against various virus infections by targeting hub proteins in the IFN-I signaling transduction pathway. We also present a future perspective on the roles of DUB-substrate interaction networks in innate antiviral activities, discuss the promises and challenges of DUB-based drug development, and identify the open questions that remain to be clarified. Our review provides a comprehensive description of DUBs, particularly their differential mechanisms that have evolved in the host to regulate IFN-I-signaling-mediated antiviral responses.</p>
引用
收藏
页数:16
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