Wang Zhifu, Wang Qi, Li Shihua, Li Xiao-Jiang, Yang Weili, He Dajian
Guangdong Key Laboratory of Non-human Primate Research, Guangdong-Hongkong-Macau Institute of CNS Regeneration, Jinan University, Guangzhou, China.
Front Aging Neurosci. 2023 Jan 10;14:1065183. doi: 10.3389/fnagi.2022.1065183. eCollection 2022.
Alzheimer's disease (AD) and Parkinson's disease (PD) are the most common neurodegenerative diseases, characterized by gradual and selective loss of neurons in the central nervous system. They affect more than 50 million people worldwide, and their incidence increases with age. Although most cases of AD and PD are sporadic, some are caused by genetic mutations that are inherited. Both sporadic and familial cases display complex neuropathology and represent the most perplexing neurological disorders. Because of the undefined pathogenesis and complex clinical manifestations, there is still no effective treatment for both AD and PD. Understanding the pathogenesis of these important neurodegenerative diseases is important for developing successful therapies. Increasing evidence suggests that microglial autophagy is associated with the pathogenesis of AD and PD, and its dysfunction has been implicated in disease progression. In this review, we focus on the autophagy function in microglia and its dysfunction in AD and PD disease models in an attempt to help our understanding of the pathogenesis and identifying new therapeutic targets of AD and PD.
阿尔茨海默病(AD)和帕金森病(PD)是最常见的神经退行性疾病,其特征是中枢神经系统中的神经元逐渐且选择性地丧失。它们在全球影响着超过5000万人,并且发病率随年龄增长而增加。尽管大多数AD和PD病例是散发性的,但有些是由遗传突变引起的遗传性病例。散发性和家族性病例均表现出复杂的神经病理学特征,是最令人困惑的神经系统疾病。由于发病机制不明且临床表现复杂,AD和PD目前仍无有效的治疗方法。了解这些重要神经退行性疾病的发病机制对于开发成功的治疗方法至关重要。越来越多的证据表明,小胶质细胞自噬与AD和PD的发病机制有关,其功能障碍与疾病进展有关。在本综述中,我们重点关注小胶质细胞中的自噬功能及其在AD和PD疾病模型中的功能障碍,以期帮助我们理解AD和PD的发病机制并确定新的治疗靶点。