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载脂蛋白E的分子生物学

Molecular biology of apolipoprotein E.

作者信息

Strittmatter Warren J, Bova Hill Carol

机构信息

Deane Laboratory, Division of Neurology, Duke Medical Center, Durham, North Carolina 27710, USA.

出版信息

Curr Opin Lipidol. 2002 Apr;13(2):119-23. doi: 10.1097/00041433-200204000-00002.

Abstract

Apolipoprotein E, first identified 26 years ago as a serum protein that mediates extracellular cholesterol transport, is now known to regulate multiple additional metabolic pathways. Several clinically important disorders of the vasculature and brain are differentially caused, or modified, by the three isoforms of this protein. Apolipoprotein E was previously believed to traffic exclusively through binding cell surface receptors, endocytosis, and hydrolysis. However, recent studies reveal a variety of additional physiologically important roles for apolipoprotein E that are mediated through interactions with different families of receptors, through binding other proteins, and through other intracellular trafficking pathways and second messengers. Much research is now directed toward identifying those pathways of apolipoprotein E metabolism that are differentially regulated by the various isoforms of apolipoprotein E, with the goal of identifying the particular molecular pathways that result in vascular and neurologic disorders.

摘要

载脂蛋白E于26年前首次被鉴定为一种介导细胞外胆固醇转运的血清蛋白,如今已知它还能调节多种其他代谢途径。该蛋白的三种异构体分别以不同方式导致或改变了几种临床上重要的血管和脑部疾病。载脂蛋白E此前被认为仅通过结合细胞表面受体、内吞作用和水解作用进行转运。然而,最近的研究揭示了载脂蛋白E通过与不同受体家族相互作用、结合其他蛋白质以及通过其他细胞内转运途径和第二信使介导的多种其他重要生理作用。目前许多研究都致力于确定载脂蛋白E代谢的哪些途径受到载脂蛋白E各种异构体的不同调节,目的是找出导致血管和神经疾病的特定分子途径。

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