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载脂蛋白 B 脂蛋白在视网膜衰老和年龄相关性黄斑变性中的作用。

Apolipoprotein B-containing lipoproteins in retinal aging and age-related macular degeneration.

机构信息

Department of Ophthalmology, University of Alabama School of Medicine, Birmingham, AL, USA.

出版信息

J Lipid Res. 2010 Mar;51(3):451-67. doi: 10.1194/jlr.R002238. Epub 2009 Sep 29.

Abstract

The largest risk factor for age-related macular degeneration (ARMD) is advanced age. With aging, there is a striking accumulation of neutral lipids in Bruch's membrane (BrM) of normal eye that continues through adulthood. This accumulation has the potential to significantly impact the physiology of the retinal pigment epithelium (RPE). It also ultimately leads to the creation of a lipid wall at the same locations where drusen and basal linear deposit, the pathognomonic extracellular, lipid-containing lesions of ARMD, subsequently form. Here, we summarize evidence obtained from light microscopy, ultrastructural studies, lipid histochemistry, assay of isolated lipoproteins, and gene expression analysis. These studies suggest that lipid deposition in BrM is at least partially due to accumulation of esterified cholesterol-rich, apolipoprotein B-containing lipoprotein particles produced by the RPE. Furthermore, we suggest that the formation of ARMD lesions and their aftermath may be a pathological response to the retention of a sub-endothelial apolipoprotein B lipoprotein, similar to a widely accepted model of atherosclerotic coronary artery disease (Tabas, I., K. J. Williams, and J. Borén. 2007. Subendothelial lipoprotein retention as the initiating process in atherosclerosis: update and therapeutic implications. Circulation. 116:1832-1844). This view provides a conceptual basis for the development of novel treatments that may benefit ARMD patients in the future.

摘要

年龄相关性黄斑变性(AMD)的最大风险因素是年龄增长。随着年龄的增长,正常眼睛的 Bruch 膜(BrM)中会明显积累中性脂质,这种积累会持续到成年。这种积累有可能对视网膜色素上皮(RPE)的生理学产生重大影响。它最终会导致在相同位置形成脂质壁,而 AMD 的特征性细胞外脂质性病变——玻璃膜疣和基底线性沉积也会随后形成。在这里,我们总结了从光镜、超微结构研究、脂质组织化学、分离脂蛋白的测定和基因表达分析中获得的证据。这些研究表明,BrM 中的脂质沉积至少部分是由于 RPE 产生的酯化胆固醇丰富、载脂蛋白 B 含脂蛋白颗粒的积累所致。此外,我们认为 AMD 病变的形成及其后果可能是对亚内皮载脂蛋白 B 脂蛋白的保留的病理反应,类似于广泛接受的动脉粥样硬化性冠状动脉疾病的模型(Tabas,I.,K. J. Williams 和 J. Borén. 2007. 动脉粥样硬化起始过程中的亚内皮脂蛋白滞留:更新和治疗意义。循环。116:1832-1844)。这种观点为开发新的治疗方法提供了概念基础,这些方法可能会使未来的 AMD 患者受益。

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