E3 ubiquitin ligase RNF5 attenuates pathological cardiac hypertrophy through STING

被引:10
|
作者
Yang, Lu-Lu [1 ]
Xiao, Wen-Chang [2 ]
Li, Huan [1 ]
Hao, Zheng-Yang [1 ]
Liu, Gui-Zhi [1 ]
Zhang, Dian-Hong [1 ]
Wu, Lei-Ming [1 ]
Wang, Zheng [1 ]
Zhang, Yan-Qing [1 ]
Huang, Zhen [1 ]
Zhang, Yan-Zhou [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Cardiovasc Hosp, Zhengzhou 450052, Peoples R China
[2] Huanggang Cent Hosp, Huanggang Inst Translat Med, Dept Cardiovasc Surg, Huanggang 438000, Peoples R China
基金
中国国家自然科学基金;
关键词
RETICULUM-ASSOCIATED DEGRADATION; QUALITY-CONTROL; EXPRESSION; PROTEINS; ROLES; RMA1;
D O I
10.1038/s41419-022-05231-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ring-finger protein 5 (RNF5) is an E3 ubiquitin ligase which is expressed in a variety of human tissues. RNF5 is involved in the regulation of endoplasmic reticulum stress, inflammation, and innate immunity and plays an important role in the occurrence and development of various tumors. However, the role of RNF5 in cardiac hypertrophy has not been reported. In this study, we found the expression of RNF5 was increased in the hearts of mice with pathological cardiac hypertrophy. The loss-of-function research demonstrated that RNF5 deficiency exacerbated cardiac hypertrophy, whereas gain-of-function studies revealed that overexpression of RNF5 had opposite effects. The stimulator of interferon genes (STING) is a signaling molecule that can activate type I interferon immunity, which can meditate inflammation and immune response in many diseases. The protein-protein interaction experiments confirmed that STING interacted with RNF5. Further studies showed that RNF5 inhibited cardiac hypertrophy by promoting STING degradation through K48-linked polyubiquitination. Therefore, we defined RNF5 as importantly regulated signaling for cardiac hypertrophy.
引用
收藏
页数:12
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