Uniporter公司
线粒体
小檗碱
调节器
细胞生物学
钙
化学
药理学
生物
生物化学
胞浆
酶
有机化学
基因
作者
Haixin Zhao,Siqi Chen,Nian Cao,Wenjun Wu,Guangqin Liu,Junwei Gao,Jiayi Chen,Ting Li,Dingyi Lu,Lingmin Zeng,Hai-Zhen Zhu,Weina Zhang,Qing Xia,Teng Li,Tao Zhou,Xuemin Zhang,Ailing Li,Xin Pan
标识
DOI:10.1002/advs.202412311
摘要
The mitochondrial calcium uniporter (MCU) complex mediates Ca2+ entry into mitochondria, which plays a crucial role in regulating cellular energy metabolism and apoptosis. Dysregulation of MCU is implicated in various diseases, such as neurodegenerative disorders, cardiac diseases, and cancer. Despite its importance, developing specific and clinically viable MCU inhibitors is challenging. Here, Berberine, a well-established drug with a documented safety profile, is identified as a potent MCU inhibitor through a virtual screening of an FDA-approved drug library. Berberine localizes within mitochondria and directly binds to the juxtamembrane loop domain of MCU. This binding disrupts the interaction of MCU with its essential regulator, EMRE, thereby inhibiting rapid Ca2+ entry into the mitochondria. Notably, Berberine pretreatment reduces mitochondrial Ca2+ overload and mitigates ischemia/reperfusion-induced myocardial injury in mice. These findings establish Berberine as a potent MCU inhibitor, offering a safe therapeutic strategy for diseases associated with dysregulated mitochondrial calcium homeostasis.
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