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首页> 外文期刊>Investigative ophthalmology & visual science >Acute and Protracted Cell Death in Light-Induced Retinal Degeneration in the Canine Model of Rhodopsin Autosomal Dominant Retinitis Pigmentosa
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Acute and Protracted Cell Death in Light-Induced Retinal Degeneration in the Canine Model of Rhodopsin Autosomal Dominant Retinitis Pigmentosa

机译:在视紫红质常染色体显性视网膜炎色素性皮炎犬模型中光诱导的视网膜变性的急性和长期细胞死亡。

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Purpose: To characterize a light damage paradigm and establish structural and immunocytochemical measures of acute and protracted light-induced retinal degeneration in the rhodopsin (RHO) T4R dog model of RHOa??autosomal dominant retinitis pigmentosa (ADRP). Methods: Retinal light damage was induced in mutant dogs with a 1-minute exposure to various light intensities (0.1a??1.0 mW/cm2) delivered with a Ganzfeld stimulator, or by fundus photography. Photoreceptor cell death was assessed by TUNEL assay, and alterations in retinal layers were examined by histology and immunohistochemistry 24 hours and 2 weeks after light exposure. Detailed topographic maps were made to document changes in the outer retinal layers of all four retinal quadrants 2 weeks post exposure. Results: Twenty-four hours post light exposure, the severity of photoreceptor cell death was dose dependent. Immunohistochemical analysis revealed disruption of rod outer segments, focal loss of the RPE integrity, and an increase in expression of endothelin receptor B in M??ller cells with the two highest doses of light and fundus photography. Two weeks after light exposure, persistence of photoreceptor death, thinning of the outer nuclear layer, and induction of M??ller cell gliosis occurred with the highest doses of light. Conclusions: We have characterized outcome measures of acute and continuing retinal degeneration in the RHO T4R dog following light exposure. These will be used to assess the molecular mechanisms of light-induced damage and rescue strategies in this large animal model of RHO-ADRP.
机译:目的:在RHOa ??常染色体显性遗传性视网膜色素变性(ADRP)的视紫红质(RHO)T4R狗模型中,鉴定光损伤范例并建立急性和长期光诱导的视网膜变性的结构和免疫细胞化学方法。方法:在用甘兹菲尔德刺激器或眼底照相术照射各种光强度(0.1a ?? 1.0 mW / cm2)1分钟的突变犬中,对视网膜光造成损伤。曝光后24小时和2周,通过TUNEL测定评估光感受器细胞死亡,并通过组织学和免疫组织化学检查视网膜层的改变。制作详细的地形图以记录暴露后2周所有四个视网膜象限的视网膜外层的变化。结果:光照后二十四小时,感光细胞死亡的严重程度与剂量有关。免疫组织化学分析显示,在两次最高剂量的光和眼底照相下,M ?? ller细胞中杆外部节段破裂,RPE完整性局灶性丧失以及内皮素受体B的表达增加。曝光两周后,在最大剂量的光下,光感受器死亡持续存在,外核层变薄,并诱发M?ller细胞神经胶质细胞增生。结论:我们已经表征了暴露于RHO T4R犬中急性和持续性视网膜变性的结果指标。这些将用于评估这种RHO-ADRP大型动物模型中光诱导的损伤的分子机制和挽救策略。

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