粒体自噬
品脱1
自噬
帕金
疾病
神经科学
视神经肽
遗传模型
生物
医学
帕金森病
脱氮酶
细胞生物学
肌萎缩侧索硬化
受体
神经退行性变
机制(生物学)
生物信息学
多巴胺能
药理学
表型
基因
作者
Ying Xu,Keshuo Jin,Jiaqing Chen,Zhongding Li,Zhenhu Zhu,Xian Su,Jiangyun Shen,Bincheng Zhou,Z. Alexander Cao,Liyan Lou,Deyu Deng,Jianzhao Zhang,Baohua Liu,Yangping Shentu,X Wang
标识
DOI:10.1073/pnas.2516471123
摘要
Parkinson's disease (PD) is a progressive neurodegenerative disease that casts a significant shadow over global health and the identification of therapeutic targets for PD will empower more effective clinical treatment. The gene encoding the deubiquitinating enzyme USP25 has been identified as a susceptible locus for PD, but the role of USP25 in PD remains unknown. In this study, we found that USP25 exacerbated dopaminergic neuronal loss and motor deficits in murine models of PD by sabotaging the mitophagy machinery. USP25 physically interacted with the autophagy receptor optineurin and disrupted its linkage with K63-specific polyubiquitin chains, leading to impaired mitophagy and the accumulation of damaged mitochondria. Genetic ablation or pharmacological inhibition of USP25 significantly restored mitophagy and thereby impeded the neurodegenerative progression in PD model mice. Collectively, our results unravel a pivotal role of USP25 in PD and identify USP25 as a pharmacological target for the development of PD drugs.
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