TFEB
溶酶体
自噬
生物
PSEN1型
细胞生物学
生物发生
阿尔茨海默病
疾病
神经科学
淀粉样前体蛋白
生物化学
医学
内科学
酶
基因
细胞凋亡
作者
Limin Yin,Yu Zhou,Hong Liu,Yang Li
出处
期刊:Autophagy
[Informa]
日期:2022-10-10
卷期号:19 (6): 1863-1864
被引量:2
标识
DOI:10.1080/15548627.2022.2131247
摘要
More than 55 million people are suffering from Alzheimer's disease (AD), but there is still no effective treatment for it. Therefore, novel therapeutic approaches and regulatory mechanisms of protein quality control need to be further evaluated and dissected. The lysosome is one of the major degradative organelles that maintain cellular homeostasis and protein quality control. In our recent study, we have identified a group of LYsosome-Enhancing Compounds (LYECs), which significantly promote the activation of TFEB (transcription factor EB) and lysosome biogenesis via inhibiting dopamine transporters (DAT). Injection of LH2-051, a member of the LYECs identified in this study, significantly improves learning, memory, and cognitive function of APP-PSEN1 mice, in which the enhanced capability of lysosomal degradation promotes the clearance of amyloid protein aggregates. In summary, this study reports novel mechanisms of neurotransporter-mediated lysosome biogenesis and shows that DAT inhibition can alleviate the pathogenesis of Alzheimer's disease.
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