TFEB
自噬
生物发生
疾病
帕金森病
碱性螺旋-环-螺旋-亮氨酸拉链转录因子
转录因子
溶酶体
神经科学
生物
医学
遗传学
基因
DNA结合蛋白
生物化学
病理
细胞凋亡
酶
作者
Jing Yang,Wei Zhang,Shugeng Zhang,Ashok Iyaswamy,Jichao Sun,Jigang Wang,Chuanbin Yang
出处
期刊:Aging and Disease
[Buck Institute for Research on Aging]
日期:2023-01-01
卷期号:14 (3): 652-652
被引量:37
标识
DOI:10.14336/ad.2022.0927
摘要
A key pathological feature of neurodegenerative diseases (NDs) such as Alzheimer's disease (AD) and Parkinson's disease (PD) is the accumulation of aggregated and misfolded protein aggregates with limited effective therapeutic agents. TFEB (transcription factor EB), a key regulator of lysosomal biogenesis and autophagy, plays a pivotal role in the degradation of protein aggregates and has thus been regarded as a promising therapeutic target for these NDs. Here, we systematically summarize the molecular mechanisms and function of TFEB regulation. We then discuss the roles of TFEB and autophagy-lysosome pathways in major neurodegenerative diseases including AD and PD. Finally, we illustrate small molecule TFEB activators with protective roles in NDs animal models, which show great potential for being further developed into novel anti-neurodegenerative agents. Overall, targeting TFEB for enhancing lysosomal biogenesis and autophagy may represent a promising opportunity for the discovery of disease-modifying therapeutics for neurodegenerative disorders though more in-depth basic and clinical studies are required in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI