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干性年龄相关性黄斑变性(AMD)小鼠模型的视网膜超微结构。

Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD).

机构信息

Immunopathology Section, Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, MD 20892-1857, USA.

出版信息

Prog Retin Eye Res. 2010 May;29(3):169-90. doi: 10.1016/j.preteyeres.2010.02.002. Epub 2010 Mar 3.

Abstract

Age-related macular degeneration (AMD) is the most prevalent form of irreversible blindness worldwide in the elderly population. The pathology of dry AMD consists of macular degeneration of photoreceptors and the RPE, lipofuscin (A2E) accumulation, and drusen formation. Mice have been widely used for generating models that simulate human AMD features for investigating the pathogenesis, treatment and prevention of the disease. Although the mouse has no macula, focal atrophy of photoreceptors and RPE, lipofuscin accumulation, and increased A2E can develop in aged mouse eyes. However, drusen are rarely seen in mice because of their simpler Bruch's membrane and different process of lipofuscin extrusion compared with humans. Thus, analyzing basal deposits at the ultrastructural level and understanding the ultrastructural pathologic differences between various mouse AMD models are critical to comprehending the significance of research findings and response to possible therapeutic options for dry AMD. Based on the multifactorial pathogenesis of AMD, murine dry AMD models can be classified into three groups. First, genetically engineered mice that target genes related to juvenile macular dystrophies are the most common models, and they include abcr(-/-) (Stargardt disease), transgenic ELOVL4 (Stargardt-3 dominant inheritary disease), Efemp1(R345W/R345W) (Doyne honeycomb retinal dystrophy), and Timp3(S156C/S156C) (Sorsby fundus dystrophy) mice. Other murine models target genes relevant to AMD, including inflammatory genes such as Cfh(-/-), Ccl2(-/-), Ccr2(-/-), Cx3cr1(-/-), and Ccl2(-/-)/cx3cr1(-/-), oxidative stress associated genes such as Sod1(-/-) and Sod2 knockdown, metabolic pathway genes such as neprilysin(-/-) (amyloid beta), transgenic mcd/mcd (cathepsin D), Cp(-/-)/Heph(-/Y) (ferroxidase ceruloplasmin/hepaestin, iron metabolism), and transgenic ApoE4 on high fat and high cholesterol diet (lipid metabolism). Second, mice have also been immunologically manipulated by immunization with carboxyethylpyrrole (CEP), an oxidative fragment of DHA found in drusen, and found to present with dry AMD features. Third, natural mouse strains such as arrd2/arrd2 (Mdm gene mutation) and the senescence accelerated mice (SAM) spontaneously develop features of dry AMD like photoreceptor atrophy and thickening of Bruch's membrane. All the aforementioned models develop retinal lesions with various features that simulate dry AMD lesions: focal photoreceptor degeneration, abnormal RPE with increased lipofuscin, basal infolding, decreased melanosomes and degeneration. However, Bruch's membrane changes are less common. Most mice develop retinal lesions at an older age (6-24 months, depending on the models), while the Ccl2(-/-)/cx3cr1(-/-) mice develop lesions by 4-6 weeks. Although murine models present various degrees of retinal and/or RPE degeneration, classical drusen is extremely rare. Using electron microscopy, small drusenoid deposits are found between RPE and Bruch's membrane in a few models including Efemp1(R345W/R345W), Ccl2(-/-)/cx3cr1(-/-), neprilysin(-/-), transgenic mcd/mcd, and ApoE4 transgenic mice on a high fat diet. High A2E levels are measured in the retinas of abcr(-/-), transgenic ELOVL4, and Ccl2(-/-)/cx3cr1(-/-) mice. In summary, murine models provide useful tools for studying AMD pathogenesis and evaluating novel therapies for this disease. This review compares the major dry AMD murine models and discusses retinal pathology at the ultrastructural level.

摘要

年龄相关性黄斑变性(AMD)是全球老年人群中最常见的不可逆失明形式。干性 AMD 的病理学包括光感受器和 RPE 的黄斑变性、脂褐素(A2E)积累和玻璃膜疣形成。小鼠已被广泛用于生成模拟人类 AMD 特征的模型,以研究疾病的发病机制、治疗和预防。尽管小鼠没有黄斑,但在老年小鼠眼中可以发展出光感受器和 RPE 的局灶性萎缩、脂褐素积累和 A2E 增加。然而,由于其 Bruch 膜更简单,脂褐素排出过程与人类不同,因此在小鼠中很少见到玻璃膜疣。因此,分析超微结构水平的基底沉积物,并了解各种小鼠 AMD 模型的超微结构病理差异,对于理解干性 AMD 研究结果的意义和对干性 AMD 可能的治疗选择的反应至关重要。基于 AMD 的多因素发病机制,可将小鼠干性 AMD 模型分为三组。首先,针对与青少年黄斑营养不良相关基因的基因工程小鼠是最常见的模型,包括 abcr(-/-)(斯塔加特病)、转 ELOVL4(斯塔加特 3 型显性遗传疾病)、Efemp1(R345W/R345W)(多尼蜂窝状视网膜营养不良)和 Timp3(S156C/S156C)(索斯比眼底营养不良)小鼠。其他小鼠模型针对与 AMD 相关的基因,包括炎症基因如 Cfh(-/-)、Ccl2(-/-)、Ccr2(-/-)、Cx3cr1(-/-)和 Ccl2(-/-)/cx3cr1(-/-)、氧化应激相关基因如 Sod1(-/-)和 Sod2 敲低、代谢途径基因如 Neprilysin(-/-)(淀粉样β)、转 mcd/mcd(组织蛋白酶 D)、Cp(-/-)/Heph(-/Y)(铁氧化酶铜蓝蛋白/肝铁蛋白、铁代谢)和转 ApoE4 高脂高胆固醇饮食(脂质代谢)。其次,还通过用羧乙基吡咯(DHA 中的氧化片段)免疫小鼠来免疫小鼠,发现其具有干性 AMD 的特征。第三,自然小鼠品系如 arrd2/arrd2(Mdm 基因突变)和衰老加速小鼠(SAM)自发发展出与干性 AMD 相似的特征,如光感受器萎缩和 Bruch 膜增厚。所有上述模型都发展出具有各种特征的视网膜病变,模拟干性 AMD 病变:局灶性光感受器变性、异常 RPE 伴脂褐素增加、基底内折、黑色素体减少和变性。然而,Bruch 膜变化较少见。大多数小鼠在老年时(6-24 个月,取决于模型)发展出视网膜病变,而 Ccl2(-/-)/cx3cr1(-/-)小鼠在 4-6 周时发展出病变。尽管小鼠模型表现出不同程度的视网膜和/或 RPE 变性,但经典的玻璃膜疣极为罕见。使用电子显微镜,在 Efemp1(R345W/R345W)、Ccl2(-/-)/cx3cr1(-/-)、Neprilysin(-/-)、转 mcd/mcd 和高脂肪饮食的 ApoE4 转基因小鼠等几种模型中,在 RPE 和 Bruch 膜之间发现了小的玻璃膜疣样沉积物。在 abcr(-/-)、转 ELOVL4 和 Ccl2(-/-)/cx3cr1(-/-)小鼠的视网膜中测量到高 A2E 水平。总之,小鼠模型为研究 AMD 的发病机制和评估该疾病的新疗法提供了有用的工具。本综述比较了主要的干性 AMD 小鼠模型,并讨论了超微结构水平的视网膜病理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/728b/2854213/f4f3674f5b8b/nihms185960f1.jpg

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