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载脂蛋白E4神经毒性的分子和细胞机制及潜在治疗策略。

Molecular and cellular mechanisms of apolipoprotein E4 neurotoxicity and potential therapeutic strategies.

作者信息

Huang Yadong

机构信息

Gladstone Institute of Neurological Disease, University of California, San Francisco, 1650 Owens Street, San Francisco, CA 94158, USA.

出版信息

Curr Opin Drug Discov Devel. 2006 Sep;9(5):627-41.

Abstract

Apolipoprotein (apo) E is a multifunctional protein that has central roles in lipid metabolism and neurobiology. It has three common isoforms (apoE2, apoE3 and apoE4) that have different effects on lipid and neuronal homneostasis. Unlike apoE3, tie most common isoform, apoE4 is a major risk factor for Alzheimer's disease (AD). Although the mechanisms underlying the actions of apoE4 in AD pathogenesis are still poorly understood, emerging data strongly suggest that apoE4, with its multiple cellular origins and multiple structural and biophysical properties, contributes to this disease by interacting with different factors through various pathways. Thus, multiple molecular and cellular mechanisms should be considered in developing anti-AD drugs that target apoE4.

摘要

载脂蛋白(apo)E是一种多功能蛋白质,在脂质代谢和神经生物学中起核心作用。它有三种常见的异构体(apoE2、apoE3和apoE4),对脂质和神经元稳态有不同影响。与最常见的异构体apoE3不同,apoE4是阿尔茨海默病(AD)的主要危险因素。尽管apoE4在AD发病机制中的作用机制仍知之甚少,但新出现的数据强烈表明,apoE4具有多种细胞来源以及多种结构和生物物理特性,通过各种途径与不同因素相互作用,从而导致这种疾病。因此,在开发针对apoE4的抗AD药物时,应考虑多种分子和细胞机制。

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