KEAP1型
炎症
脂质过氧化
基因剔除小鼠
化学
细胞生物学
体内
泡沫电池
药理学
细胞
氧化应激
体外
生物
医学
癌症研究
免疫学
生物化学
转录因子
巨噬细胞
受体
基因
生物技术
作者
Yun Zhao,Guobin Zheng,Shu Yang,Shangjing Liu,Yifan Wu,Yaodong Miao,Zhen Liang,Yunqing Hua,Jing Zhang,Jia Shi,Dan Li,Yanfei Cheng,Yunsha Zhang,Yuanli Chen,Guanwei Fan,Chuanrui Ma
摘要
PNS 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.
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