Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, United States.
Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Invest Ophthalmol Vis Sci. 2018 Mar 20;59(4):AMD143-AMD151. doi: 10.1167/iovs.18-24245.
Geographic atrophy (GA) is the late stage of non-neovascular age-related macular degeneration. A lack of animal models for GA has hampered treatment efforts. Presented herein is a rat model for GA using subretinal injection of sodium iodate (NaIO3).
Rats were given subretinal injections of NaIO3 (5 μg/μL) using a pico-injector. Fundus photographs and spectral domain optical coherent tomography scans were collected at 1, 3, 7, 14, and 28 days after injection, at which time rats were euthanized and eyes were enucleated. Eyes were either cryopreserved or dissected into retinal and choroidal flatmounts. Fluorescence immunohistochemistry was performed for retinal glial fibrillary acidic protein (activated Müller cells and astrocytes) and vimentin (Müller cells), as well as peanut agglutin lectin (photoreceptors) labeling. RPE/choroids were labeled for RPE65 and CD34. Images were collected on Zeiss confocal microscopes.
Fundus photos, spectral domain optical coherent tomography, and RPE65 staining revealed well-demarcated areas with focal loss of RPE and photoreceptors in NaIO3-treated rats. At 1 day after injection, RPE cells appeared normal. By 3 days, there was patchy RPE and photoreceptor loss in the injected area. RPE and photoreceptors were completely degenerated in the injected area by 7 days. A large subretinal glial membrane occupied the degenerated area. Choriocapillaris was highly attenuated in the injected area at 14 and 28 days.
The rat model reported herein mimics the photoreceptor cell loss, RPE atrophy, glial membrane formation, and choriocapillaris degeneration seen in GA. This model will be valuable for developing and testing drugs and progenitor cell regenerative therapies for GA.
地理萎缩(GA)是年龄相关性黄斑变性的晚期非新生血管期。由于缺乏 GA 的动物模型,治疗工作受到阻碍。本文介绍了一种通过视网膜下注射碘酸钠(NaIO3)制作 GA 大鼠模型的方法。
大鼠通过皮内注射器接受 NaIO3(5μg/μL)的视网膜下注射。在注射后 1、3、7、14 和 28 天收集眼底照片和光谱域光相干断层扫描扫描,此时处死大鼠并眼球摘出。眼球要么冷冻保存,要么解剖成视网膜和脉络膜平面。进行视网膜神经胶质原纤维酸性蛋白(激活的 Müller 细胞和星形胶质细胞)和波形蛋白(Müller 细胞)以及花生凝集素(感光细胞)标记的荧光免疫组织化学染色。对 RPE/脉络膜进行 RPE65 和 CD34 标记。在蔡司共聚焦显微镜上采集图像。
眼底照片、光谱域光相干断层扫描和 RPE65 染色显示,在 NaIO3 处理的大鼠中,边界清晰的区域出现局灶性 RPE 和感光细胞丧失。注射后 1 天,RPE 细胞外观正常。到第 3 天,注射区域出现斑块状 RPE 和感光细胞丧失。到第 7 天,注射区域的 RPE 和感光细胞完全退化。一个大的视网膜下胶质膜占据了退化区域。在注射后 14 和 28 天,注射区域的脉络膜毛细血管高度衰减。
本文报道的大鼠模型模拟了 GA 中观察到的感光细胞丧失、RPE 萎缩、胶质膜形成和脉络膜毛细血管退化。该模型将对开发和测试 GA 的药物和祖细胞再生疗法具有重要价值。