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Aging, age-related macular degeneration, and the response-to-retention of apolipoprotein B-containing lipoproteins.衰老、年龄相关性黄斑变性与载载脂蛋白 B 脂蛋白的滞留反应
Prog Retin Eye Res. 2009 Nov;28(6):393-422. doi: 10.1016/j.preteyeres.2009.08.001. Epub 2009 Aug 19.
2
A human apoB100 transgenic mouse expresses human apoB100 in the RPE and develops features of early AMD.一种人载脂蛋白B100转基因小鼠在视网膜色素上皮细胞中表达人载脂蛋白B100,并出现早期年龄相关性黄斑变性的特征。
Exp Eye Res. 2009 Jun;88(6):1115-23. doi: 10.1016/j.exer.2009.01.017. Epub 2009 Feb 7.
3
Antivascular endothelial growth factor therapy for neovascular age-related macular degeneration.抗血管内皮生长因子疗法治疗新生血管性年龄相关性黄斑变性
Curr Opin Ophthalmol. 2009 May;20(3):158-65. doi: 10.1097/ICU.0b013e32832d25b3.
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Esterified cholesterol is highly localized to Bruch's membrane, as revealed by lipid histochemistry in wholemounts of human choroid.酯化胆固醇高度定位于布鲁赫膜,这是通过对人脉络膜整体标本进行脂质组织化学分析得出的结果。
J Histochem Cytochem. 2009 Aug;57(8):731-9. doi: 10.1369/jhc.2009.953448. Epub 2009 Apr 13.
5
Bruch's membrane changes in transgenic mice overexpressing the human biglycan and apolipoprotein b-100 genes.过表达人双糖链蛋白聚糖和载脂蛋白b - 100基因的转基因小鼠中布鲁赫膜的变化。
Exp Eye Res. 2009 Aug;89(2):178-86. doi: 10.1016/j.exer.2009.03.006. Epub 2009 Mar 24.
6
New components of 'basal laminar deposits' in age-related macular degeneration.年龄相关性黄斑变性中“基底膜沉积物”的新成分
Cells Tissues Organs. 2009;190(3):170-81. doi: 10.1159/000187632. Epub 2008 Dec 17.
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Blood-retinal barrier in hypoxic ischaemic conditions: basic concepts, clinical features and management.缺氧缺血状态下的血视网膜屏障:基本概念、临床特征与管理
Prog Retin Eye Res. 2008 Nov;27(6):622-47. doi: 10.1016/j.preteyeres.2008.09.003. Epub 2008 Oct 4.
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7-Ketocholesterol is present in lipid deposits in the primate retina: potential implication in the induction of VEGF and CNV formation.7-酮胆固醇存在于灵长类动物视网膜的脂质沉积物中:对诱导血管内皮生长因子(VEGF)和脉络膜新生血管(CNV)形成的潜在影响。
Invest Ophthalmol Vis Sci. 2009 Feb;50(2):523-32. doi: 10.1167/iovs.08-2373. Epub 2008 Oct 20.
9
Lipoprotein particles of intraocular origin in human Bruch membrane: an unusual lipid profile.人布鲁赫膜中眼内源性脂蛋白颗粒:一种不寻常的脂质谱。
Invest Ophthalmol Vis Sci. 2009 Feb;50(2):870-7. doi: 10.1167/iovs.08-2376. Epub 2008 Sep 20.
10
Lipid and fatty acid profile of the retina, retinal pigment epithelium/choroid, and the lacrimal gland, and associations with adipose tissue fatty acids in human subjects.人类受试者视网膜、视网膜色素上皮/脉络膜和泪腺的脂质和脂肪酸谱及其与脂肪组织脂肪酸的关联。
Exp Eye Res. 2008 Dec;87(6):521-8. doi: 10.1016/j.exer.2008.08.010. Epub 2008 Aug 29.

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.

DOI:10.1194/jlr.R002238
PMID:19797256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2817575/
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。