载脂蛋白 E 在阿尔茨海默病发病机制、预后和治疗中的作用

Allison B Reiss, Mary Housny, Shelly Gulkarov, Tahmina Hossain, Brandon Locke, Ankita Srivastava, Aaron Pinkhasov, Irving H Gomolin, Thomas Wisniewski, Joshua De Leon
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摘要

阿尔茨海默病(AD)是一种无法治愈的渐进性神经退行性疾病,在全球的发病率越来越高。之前进行的抗淀粉样蛋白和抗 tau 免疫疗法试验表明,还需要对其他机制进行更多研究,以找到治疗或改变病情的疗法。载脂蛋白 E(ApoE)是脑脂代谢中的一种重要蛋白质,专门清除和转运脂质和胆固醇。载脂蛋白 E4 等位基因具有很大的基因剂量依赖性,可增加罹患注意力缺失症的风险,并降低注意力缺失症的发病年龄,但其影响机制尚不完全清楚。其他等位基因会带来不同程度的注意力缺失症风险。载脂蛋白 E2 具有保护作用,而载脂蛋白 E3 是最常见的异构体,被认为是中性的。本文概述了载脂蛋白E在注意力缺失症发病机制中作用的最新信息,重点是参与注意力缺失症发展的途径以及与大脑中不同细胞类型的关键过程之间的相互作用。阐明载脂蛋白E与大脑功能多个方面的关键相互作用有助于设计新型载脂蛋白E靶向治疗方法。
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Role of Apolipoprotein E in Alzheimer's Disease Pathogenesis, Prognosis and Treatment.

Alzheimer's disease (AD) is an incurable and progressive neurodegenerative disease with increasing prevalence worldwide. Previous trials of anti-amyloid and anti-tau immunotherapy indicate that additional research needs to be conducted on other mechanisms to find curative or disease-modifying therapy. This review focuses on apolipoprotein E (ApoE), a critical protein in brain lipid metabolism that acts specifically in the clearance and transport of lipids and cholesterol. The ApoE4 allele confers substantial gene dose-dependent risk of developing AD and lowers the age of onset of AD, although the mechanisms of influence remain incompletely understood. The other isoforms bring different levels of AD risk. ApoE2 is protective while ApoE3 is the most common isoform and is considered neutral. An overview is presented of the latest information on the role of ApoE in AD pathogenesis with an emphasis on pathways that are involved in AD development and interactions with crucial processes in different cell types in the brain. Elucidating the key interactions of ApoE with multiple aspects of brain function can be useful for designing novel ApoE-targeted therapeutic approaches.

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