OTUD4 alleviates hepatic ischemia-reperfusion injury by suppressing the K63-linked ubiquitination of TRAF6

被引:22
|
作者
Liu, Hang [1 ]
Fan, Jing [2 ]
Zhang, Wanqiu [1 ]
Chen, Qingsong [1 ]
Zhang, Yuke [1 ]
Wu, Zhongjun [1 ]
机构
[1] Chongqing Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 1, Chongqing 400010, Peoples R China
[2] Chongqing Med Univ, Dept Emergency, Affiliated Hosp 1, Chongqing 400010, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatic ischemia-reperfusion injury; OTUD4; TRAF6; K63; polyubiquitination; TOLL-LIKE RECEPTOR; LIVER ISCHEMIA; ISCHEMIA/REPERFUSION INJURY; KAPPA-B; MECHANISMS; DEUBIQUITINASE; ACTIVATION; CELLS; TAK1;
D O I
10.1016/j.bbrc.2019.12.114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatic ischemia-reperfusion (IR) injury can cause serious liver damage, leading to liver dysfunction after liver surgery, which is associated with NF-kappa B-mediated inflammation. The K63-linked auto-polyubiquitination of tumor necrosis factor receptor-associated factor 6 (TRAF6) is essential for the activation of NF-kappa B. Here, we found that OTU domain-containing protein 4 (OTUD4), a deubiquitinating enzyme (DUB), interacts with TRAF6 and decreases the K63 auto-polyubiquitination of TRAF6. In addition, the data showed that NF-kappa B activation was impaired and inflammatory factor levels were reduced after overexpressing OTUD4 in a hypoxia/reoxygenation (HR) model and a hepatic IR model. Additionally, the liver inflammatory response and tissue damage were ameliorated in mice overexpressing OTUD4. Taken together, these results show that OTUD4 can negatively regulate NF-kappa B activation by suppressing the K63-linked ubiquitination of TRAF6, thus alleviating hepatic ischemia-reperfusion injury. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:924 / 930
页数:7
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