分子生物学
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细胞培养与分析
蛋白研究
细胞因子
重组蛋白
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高通量测序建库
病原检测UCF系列
生物医药
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抑制剂激活剂与常用试剂
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USP14 promotes K63-linked RIG-I deubiquitination and suppresses antiviral immune responses

Hongrui Li, Zizhao Zhao, Jing Ling, Linhui Pan, Xibao Zhao, Huihui Zhu, Juan Yu, Bin Xie, Jianzhong Shen, Weilin Chen

Journal:EUROPEAN JOURNAL OF IMMUNOLOGY

IF:4.25

DOI:10.1002/eji.201847603

PMID:

Published:2018-11-22

research field:分子生物学免疫学病毒学

Abstract

Retinoic acid‐inducible gene I (RIG‐I) is a critical RNA virus sensor that initiates antiviral immune response through K63‐linked ubiquitination. In this study, we demonstrated USP14, a deubiquitinating enzyme, as a negative regulator in antiviral responses by directly deubiquitinating K63‐linked RIG‐I. USP14 knockdown significantly enhanced RIG‐I‐triggered type I IFN signaling and inhibited vesicular stomatitis virus (VSV) replication both in mouse peritoneal macrophages and THP1 cells. USP14 overexpression in HeLa cells attenuated RIG‐I‐triggered IFN‐β expression and promoted VSV replication. Besides, USP14‐specific inhibitor, IU1, increased RIG‐I‐mediated type I IFN production and antiviral responses in vitro and in vivo. In addition, USP14 could interact with RIG‐I and remove RIG‐I K63‐linked polyubiquitination chains. This article is the first to report that USP14 acts as a negative regulator in antiviral response through deubiquitinating K63‐linked RIG‐I. These findings provide insights into a potential new therapy targeting USP14 for RNA virus‐related diseases.

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