Department of Medicine, NYU Grossman Long Island School of Medicine, Mineola, NY 11501, USA.
Department of Foundations of Medicine, NYU Grossman Long Island School of Medicine, Mineola, NY 11501, USA.
Discov Med. 2024 Oct;36(189):1917-1932. doi: 10.24976/Discov.Med.202436189.179.
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.
阿尔茨海默病(AD)是一种无法治愈且进行性的神经退行性疾病,在全球的患病率正在不断增加。之前的抗淀粉样蛋白和抗 tau 免疫疗法的临床试验表明,需要对其他机制进行更多的研究,以找到有治愈或疾病修饰作用的治疗方法。本综述重点关注载脂蛋白 E(ApoE),这是一种大脑脂质代谢中的关键蛋白,特异性地在脂质和胆固醇的清除和运输中发挥作用。ApoE4 等位基因赋予了大量的、基因剂量依赖性的 AD 发病风险,并降低了 AD 的发病年龄,尽管其影响机制仍不完全清楚。其他同工型则带来了不同程度的 AD 发病风险。ApoE2 具有保护作用,而 ApoE3 是最常见的同工型,被认为是中性的。本文综述了 ApoE 在 AD 发病机制中的最新信息,重点介绍了与 AD 发展相关的途径以及与大脑不同细胞类型中关键过程的相互作用。阐明 ApoE 与大脑功能多个方面的关键相互作用,有助于设计新的 ApoE 靶向治疗方法。