Tan Chen-Chen, Yu Jin-Tai, Tan Meng-Shan, Jiang Teng, Zhu Xi-Chen, Tan Lan
Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, China.
Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, China; Department of Neurology, Qingdao Municipal Hospital, College of Medicine and Pharmaceutics, Ocean University of China, Qingdao, China; Department of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Qingdao, China.
Neurobiol Aging. 2014 May;35(5):941-57. doi: 10.1016/j.neurobiolaging.2013.11.019. Epub 2013 Nov 28.
Neurodegenerative diseases, such as Alzheimer's disease Parkinson's disease, Huntington's disease, and amyotrophic lateral sclerosis, share a common cellular and molecular pathogenetic mechanism involving aberrant misfolded protein or peptide aggregation and deposition. Autophagy represents a major route for degradation of aggregated cellular proteins and dysfunctional organelles. Emerging studies have demonstrated that up-regulation of autophagy can lead to decreased levels of these toxic aggregate-prone proteins, and is beneficial in the context of aging and various models of neurodegenerative diseases. Understanding the signaling pathways involved in the regulation of autophagy is crucial to the development of strategies for therapy. This review will discuss the cellular and molecular mechanisms of autophagy and its important role in the pathogenesis of aging and neurodegenerative diseases, and the ongoing drug discovery strategies for therapeutic modulation.
神经退行性疾病,如阿尔茨海默病、帕金森病、亨廷顿病和肌萎缩侧索硬化症,具有共同的细胞和分子致病机制,涉及异常错误折叠的蛋白质或肽聚集和沉积。自噬是细胞内聚集蛋白和功能失调细胞器降解的主要途径。新兴研究表明,自噬上调可导致这些易于聚集的毒性蛋白水平降低,并且在衰老和各种神经退行性疾病模型中具有益处。了解参与自噬调节的信号通路对于开发治疗策略至关重要。本综述将讨论自噬的细胞和分子机制及其在衰老和神经退行性疾病发病机制中的重要作用,以及正在进行的治疗性调节药物发现策略。