The plant extract PNS mitigates atherosclerosis via promoting Nrf2-mediated inhibition of ferroptosis through reducing USP2-mediated Keap1 deubiquitination

被引:0
|
作者
Zhao, Yun [1 ]
Zheng, Guobin [2 ]
Yang, Shu [3 ]
Liu, Shangjing [1 ]
Wu, Yifan [1 ]
Miao, Yaodong [4 ]
Liang, Zhen [3 ]
Hua, Yunqing [1 ]
Zhang, Jing [1 ]
Shi, Jia [1 ]
Li, Dan [1 ]
Cheng, Yanfei [1 ]
Zhang, Yunsha [1 ]
Chen, Yuanli [5 ]
Fan, Guanwei [1 ]
Ma, Chuanrui [1 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Teaching Hosp 1, Natl Clin Res Ctr Chinese Med Acupuncture & Moxibu, 88 Chang Ling Rd, Tianjin, Peoples R China
[2] Tianjin Med Univ, Chu Hsien I Mem Hosp & Tianjin Inst Endocrinol, Tianjin Key Lab Metab Dis, NHC Key Lab Hormones & Dev, Tianjin, Peoples R China
[3] Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen Peoples Hosp, Dept Geriatr, Shenzhen, Peoples R China
[4] Tianjin Univ Tradit Chinese Med, Affiliated Hosp 2, Tianjin, Peoples R China
[5] Hefei Univ Technol, Sch Food & Biol Engn, Nutr Regulat Anhui Dept Educ, Key Lab Major Metab Dis, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
atherosclerosis; deubiquitination; ferroptosis; Nrf2; PNS; USP2; PANAX-NOTOGINSENG SAPONINS; CONCISE GUIDE; OXIDATIVE STRESS; ACTIVATION; MECHANISM; NRF2;
D O I
10.1111/bph.17311
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and purposeAtherosclerosis is the basis of cardiovascular disease. Ferroptosis is a form of programmed cell death characterized by lipid peroxidation, which contributes to atherogenesis. The plant extract PNS (Panax notoginseng saponins), containing the main active ingredients of Panax notoginseng, exhibits anti-atherogenic properties. Herein, we determined whether PNS and its major components could attenuate atherosclerosis by suppressing ferroptosis and revealed the underlying mechanism(s).Experimental approachThe anti-atherogenic effects of PNS and their association with inhibition of ferroptosis was determined in apoE-/- mice. In vitro, the anti-ferroptotic effect and mechanism(s) of PNS components were demonstrated in the presence of ferroptosis inducers. Expression of ferroptosis markers and the ubiquitination of Keap1 were evaluated in USP2-/- macrophages. Finally, the anti-atherogenic effect of USP2 knockout was determined by using USP2-/- mice treated with high-fat diet (HFD) and AAV-PCSK9.Key resultsPNS inhibited ferroptosis and atherosclerosis in vivo. PNS suppressed ferroptosis and ferroptosis-aggravated foam cell formation and inflammation in vitro. Mechanistically, PNS and its components activated Nrf2 by antagonizing Keap1, which was attributed to the inhibition of USP2 expression. USP2 knockout antagonized ferroptosis and ferroptosis-aggravated foam cell formation and inflammation, thus mitigating atherosclerosis. USP2 knockout abolished inhibitory effects of PNS on foam cell formation and inflammation in vitro.Conclusion and implicationsPNS reduced USP2-mediated Keap1 de-ubiquitination and promoted Keap1 degradation, thereby activating Nrf2, improving iron metabolism and reducing lipid peroxidation, thus contributing to an anti-atherosclerotic outcome. Our study revealed the mechanism(s) underlying inhibition of ferroptosis and atherosclerosis by PNS. image
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收藏
页码:4822 / 4844
页数:23
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