溶酶体
细胞生物学
少突胶质细胞
神经科学
化学
生物
计算生物学
中枢神经系统
生物化学
髓鞘
酶
作者
Li‐Pao Fang,Ching-Hsin Lin,Yasser Medlej,Renping Zhao,Hsin‐Fang Chang,Qilin Guo,Zhonghao Wu,Yixun Su,Na Zhao,Davide Gobbo,Amanda Wyatt,Vanessa Wahl,Frédéric Di Fiore,Szu-Min Tu,Ulrich Boehm,Wenhui Huang,Shan Bian,Amit Agarwal,Marcel A. Lauterbach,Chenju Yi
标识
DOI:10.1038/s41467-025-56484-8
摘要
Abstract Oligodendrocyte precursor cells (OPCs) shape brain function through many non-canonical regulatory mechanisms beyond myelination. Here we show that OPCs form contacts with their processes on neuronal somata in a neuronal activity-dependent manner. These contacts facilitate exocytosis of neuronal lysosomes. A reduction in the number or branching of OPCs reduces these contacts, which is associated with lysosome accumulation and altered metabolism in neurons and more senescent neurons with age. A similar reduction in OPC branching and neuronal lysosome accumulation is seen in an early-stage mouse model of Alzheimer’s disease. Our findings have implications for the prevention of age-related pathologies and the treatment of neurodegenerative diseases.
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