自噬
溶酶体
泛素
蛋白酶体
细胞生物学
降级(电信)
神经科学
蛋白质降解
化学
生物
生物化学
工程类
基因
细胞凋亡
酶
电信
作者
Minjae Lee,Jung Hoon Lee,David C. Rubinsztein
标识
DOI:10.1016/j.pneurobio.2013.03.001
摘要
The ubiquitin-proteasome system (UPS) and the autophagy-lysosome system are two major protein quality control mechanisms in eukaryotic cells. While the UPS has been considered for decades as the critical regulator in the degradation of various aggregate-prone proteins, autophagy has more recently been shown to be an important pathway implicated in neuronal health and disease. The two hallmark lesions of Alzheimer's disease (AD) are extracellular β-amyloid plaques and intracellular tau tangles. It has been suggested that tau accumulation is pathologically more relevant to the development of neurodegeneration and cognitive decline in AD patients than β-amyloid plaques. Here, we review the UPS and autophagy-mediated tau clearance mechanisms and outline the biochemical connections between these two processes. In addition, we discuss pharmacological methods that target these degradation systems for the treatment and prevention of AD.
科研通智能强力驱动
Strongly Powered by AbleSci AI