The Ubiquitin E3 Ligase Parkin Inhibits Innate Antiviral Immunity Through K48-Linked Polyubiquitination of RIG-I and MDA5

被引:24
|
作者
Bu, Lang [1 ]
Wang, Huan [2 ]
Hou, Panpan [1 ]
Guo, Shuting [3 ]
He, Miao [1 ]
Xiao, Jingshu [1 ]
Li, Ping [1 ]
Zhong, Yongheng [1 ]
Jia, Penghui [1 ]
Cao, Yuanyuan [4 ]
Liang, Guanzhan [1 ]
Yang, Chenwei [1 ]
Chen, Lang [3 ]
Guo, Deyin [1 ]
Li, Chun-Mei [1 ]
机构
[1] Sun Yat Sen Univ, Sch Med, Infect & Immun Ctr TIIC, MOE Key Lab Trop Dis Control, Shenzhen, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Inst Precis Med, Guangzhou, Peoples R China
[3] Wuhan Univ, Sch Basic Med Sci, Dept Immunol, Wuhan, Peoples R China
[4] Anhui Med Univ, Sch Basic Med Sci, Hefei, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
基金
中国国家自然科学基金;
关键词
parkin; mitophagy; polyubiquitination; RIG-I; MDA5; innate immunity; KAPPA-B; PINK1; RECOGNITION; MITOPHAGY; ACTIVATION; RECEPTORS; MUTATIONS; INDUCTION; PROTEINS; PATHWAY;
D O I
10.3389/fimmu.2020.01926
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate immunity is the first-line defense against antiviral or antimicrobial infection. RIG-I and MDA5, which mediate the recognition of pathogen-derived nucleic acids, are essential for production of type I interferons (IFN). Here, we identified mitochondrion depolarization inducer carbonyl cyanide 3-chlorophenylhydrazone (CCCP) inhibited the response and antiviral activity of type I IFN during viral infection. Furthermore, we found that the PTEN-induced putative kinase 1 (PINK1) and the E3 ubiquitin-protein ligase Parkin mediated mitophagy, thus negatively regulating the activation of RIG-I and MDA5. Parkin directly interacted with and catalyzed the K48-linked polyubiquitination and subsequent degradation of RIG-I and MDA5. Thus, we demonstrate that Parkin limits RLR-triggered innate immunity activation, suggesting Parkin as a potential therapeutic target for the control of viral infection.
引用
收藏
页数:13
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