TFEB
肌萎缩侧索硬化
神经保护
生物
溶酶体
神经科学
自噬
激活剂(遗传学)
调节器
转录因子
运动神经元
药物发现
蛋白质稳态
细胞生物学
生物发生
生物信息学
机制(生物学)
神经退行性变
癌症研究
共核细胞病
治疗方法
神经肌肉接头
作者
Ang Li,Xianglu Xiao,Dajiang Qin,Huanxing Su
出处
期刊:Autophagy
[Taylor & Francis]
日期:2026-04-13
卷期号:: 1-2
标识
DOI:10.1080/15548627.2026.2659295
摘要
, we established a robust artificial intelligence (AI) - driven virtual screening pipeline and identified isoginkgetin (ISO) as a potent TFEB activator that effectively promotes lysosomal biogenesis and enhances lysosomal function. Importantly, ISO exhibits potent neuroprotective effects against motor neuron degeneration in ALS models. Using this AI-driven strategy, we identified a previously unrecognized neuroprotective mechanism by which ISO protects motor neurons through TFEB-dependent restoration of lysosomal function, validating lysosomal function as a promising therapeutic target for ALS. Collectively, this work establishes that AI-powered screening to identify mTORC1-independent TFEB agonists is a valuable paradigm for the discovery and development of therapeutic agents against ALS and other neurodegenerative diseases.
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