Nuclear Localization of Apolipoprotein E4: A New Trick for an Old Protein.

Troy T Rohn, Zachary D Moore
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Abstract

One of the most important genetic risk factors for late-onset Alzheimer's Disease (AD) is harboring the ApoE4 allele. Much is known regarding the functions of the ApoE4 protein including cholesterol transport in the CNS and a critical role in clearing beta-amyloid deposits in the AD brain. However, recent studies demonstrating the nuclear localization suggest a novel function beyond the classical known actions of ApoE4. The purpose of the current review is to examine how this secreted protein traffics to the nucleus and to discuss possible outcomes of nuclear localization in the CNS. It is suggested that proteolytic fragmentation of ApoE4 is a key step leading to nuclear localization and the outcome of this event is to initiate transcription of various genes involved in inflammation and cell death. Therefore, the nuclear localization and induction of gene expression may provide a link between harboring the ApoE4 allele and enhanced dementia risk observed in AD.

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载脂蛋白 E4 的核定位:老蛋白的新花招
携带载脂蛋白 E4 等位基因是晚发性阿尔茨海默病(AD)最重要的遗传风险因素之一。关于载脂蛋白 E4 蛋白的功能,包括在中枢神经系统中的胆固醇转运以及在清除阿兹海默症大脑中的β-淀粉样蛋白沉积物方面的关键作用,人们已经有了很多了解。然而,最近的研究表明,ApoE4 蛋白的核定位功能超出了已知的传统功能。本综述旨在研究这种分泌蛋白如何向细胞核迁移,并讨论在中枢神经系统中核定位的可能结果。有研究认为,载脂蛋白 E4 的蛋白水解片段是导致核定位的关键步骤,这一事件的结果是启动参与炎症和细胞死亡的各种基因的转录。因此,核定位和诱导基因表达可能是携带载脂蛋白E4等位基因与AD痴呆症风险增加之间的联系。
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