Suppr超能文献

Parkin 泛素 E3 连接酶通过 RIG-I 和 MDA5 的 K48 连接多泛素化抑制先天抗病毒免疫。

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

机构信息

MOE Key Laboratory of Tropical Disease Control, the Infection and Immunity Center (TIIC), School of Medicine, Sun Yat-sen University, Shenzhen, China.

Institute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

出版信息

Front Immunol. 2020 Sep 2;11:1926. doi: 10.3389/fimmu.2020.01926. eCollection 2020.

Abstract

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.

摘要

先天免疫是抗病毒或抗微生物感染的第一道防线。RIG-I 和 MDA5 介导对病原体衍生核酸的识别,对于产生 I 型干扰素 (IFN) 至关重要。在这里,我们发现线粒体去极化诱导剂羰基氰化物 3-氯苯腙 (CCCP) 在病毒感染过程中抑制了 I 型 IFN 的反应和抗病毒活性。此外,我们发现 PTEN 诱导的假定激酶 1 (PINK1) 和 E3 泛素-蛋白连接酶 Parkin 介导了线粒体自噬,从而负调控 RIG-I 和 MDA5 的激活。Parkin 直接相互作用并催化 RIG-I 和 MDA5 的 K48 连接多泛素化和随后的降解。因此,我们证明 Parkin 限制了 RLR 触发的先天免疫激活,提示 Parkin 是控制病毒感染的潜在治疗靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验