氧化应激
SOD2
视网膜变性
视网膜色素上皮
视网膜
视网膜电图
外层核层
SOD1
条件基因敲除
视网膜
病理
黄斑变性
蛋白质稳态
生物
细胞生物学
超氧化物歧化酶
医学
内分泌学
神经科学
眼科
生物化学
表型
基因
作者
Manas R. Biswal,Cristhian J. Ildefonso,Sheng Wang,Soo Jung Seo,Zhaoyang Wang,Hong Li,Yun Le,Alfred S. Lewin
标识
DOI:10.1007/978-3-319-17121-0_5
摘要
An appropriate animal model is essential to screening drugs or designing a treatment strategy for geographic atrophy. Since oxidative stress contributes to the pathological changes of the retinal pigment epithelium (RPE), we are reporting a new mouse AMD model of retinal degeneration by inducing mitochondrial oxidative stress in RPE. Sod2 the gene for manganese superoxide dismutase (MnSOD) was deleted in RPE layer using conditional knockout strategy. Fundus microscopy, SD-OCT and electroretinography were used to monitor retinal structure and function in living animals and microscopy was used to assess pathology post mortem. Tissue specific deletion of Sod2 caused elevated signs of oxidative stress, RPE dysfunction and showed some key features of AMD. Due to induction of oxidative stress, the conditional knockout mice show progressive reduction in ERG responses and thinning of outer nuclear layer (ONL) compared to non-induced littermates.
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