Facultad de Ciencias de la Salud, Universidad de Zaragoza, 50009 Zaragoza, Spain; Instituto de Investigacion Sanitaria Aragon, 50009 Zaragoza, Spain.
Instituto de Investigacion Sanitaria Aragon, 50009 Zaragoza, Spain; Adipocyte and Fat Biology Laboratory (AdipoFat), Instituto Aragonés de Ciencias de la Salud (IACS), 50009 Zaragoza, Spain.
Neurobiol Dis. 2020 May;138:104809. doi: 10.1016/j.nbd.2020.104809. Epub 2020 Feb 19.
Apolipoprotein E (APOE) is a multifunctional protein synthesized and secreted by multiple mammalian tissues. Although hepatocytes contribute about 75% of the peripheral pool, APOE can also be expressed in adipose tissue, the kidney, and the adrenal glands, among other tissues. High levels of APOE production also occur in the brain, where it is primarily synthesized by glia, and peripheral and brain APOE pools are thought to be distinct. In humans, APOE is polymorphic, with three major alleles (ε2, ε3, and ε4). These allelic forms dramatically alter APOE structure and function. Historically, the vast majority of research on APOE has centered on the important role it plays in modulating risk for cardiovascular disease and Alzheimer's disease. However, the established effects of this pleiotropic protein extend well beyond these two critical health challenges, with demonstrated roles across a wide spectrum of biological conditions, including adipose tissue function and obesity, metabolic syndrome and diabetes, fertility and longevity, and immune function. While the spectrum of biological systems in which APOE plays a role seems implausibly wide at first glance, there are some potential unifying mechanisms that could tie these seemingly disparate disorders together. In the current review, we aim to concisely summarize a wide breadth of APOE-associated pathologies and to analyze the influence of APOE in the development of several distinct disorders in order to provide insight into potential shared mechanisms implied in these various pathophysiological processes.
载脂蛋白 E(APOE)是一种多功能蛋白,由多种哺乳动物组织合成和分泌。尽管肝细胞贡献了约 75%的外周池,但 APOE 也可以在脂肪组织、肾脏和肾上腺等组织中表达。大脑中也会产生高水平的 APOE,主要由神经胶质细胞合成,而外周和大脑 APOE 池被认为是不同的。在人类中,APOE 是多态的,有三个主要等位基因(ε2、ε3 和 ε4)。这些等位基因形式极大地改变了 APOE 的结构和功能。从历史上看,对 APOE 的研究绝大多数都集中在它在调节心血管疾病和阿尔茨海默病风险方面的重要作用上。然而,这种多效蛋白的既定作用远远超出了这两个关键的健康挑战,在广泛的生物学条件下都有作用,包括脂肪组织功能和肥胖、代谢综合征和糖尿病、生育和长寿以及免疫功能。虽然 APOE 发挥作用的生物学系统范围乍一看似乎令人难以置信地广泛,但有一些潜在的统一机制可以将这些看似不同的疾病联系在一起。在当前的综述中,我们旨在简明地总结广泛的与 APOE 相关的病理学,并分析 APOE 在几种不同疾病发展中的影响,以深入了解这些各种病理生理过程中隐含的潜在共同机制。