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阿尔茨海默病转基因小鼠中β淀粉样蛋白的积累及视网膜内层退行性变化

Amyloid β accumulation and inner retinal degenerative changes in Alzheimer's disease transgenic mouse.

作者信息

Gupta Vivek K, Chitranshi Nitin, Gupta Veer B, Golzan Mojtaba, Dheer Yogita, Wall Roshana Vander, Georgevsky Dana, King Anna E, Vickers James C, Chung Roger, Graham Stuart

机构信息

Faculty of Medicine and Health sciences, Macquarie University, Australia.

Faculty of Medicine and Health sciences, Macquarie University, Australia.

出版信息

Neurosci Lett. 2016 Jun 3;623:52-6. doi: 10.1016/j.neulet.2016.04.059. Epub 2016 Apr 28.

Abstract

The APP-PS1ΔE9 mouse model of Alzheimer's disease (AD) exhibits age dependent amyloid β (Aβ) plaque formation in their central nervous system due to high expression of mutated human APP and PSEN1 transgenes. Here we evaluated Aβ deposition and changes in soluble Aβ accumulation in the retinas of aged APP-PS1 mice using a combination of immunofluorescence, retinal flat mounts and western blotting techniques. Aβ accumulation in the retina has previously been shown to be associated with retinal ganglion cell apoptosis in animal models of glaucoma. This study investigated changes in the inner retinal function and structure in APP-PS1 mice using electrophysiology and histological approaches respectively. We report for the first time a significant decline in scotopic threshold response (STR) amplitudes which represents inner retinal function in transgenic animals compared to the wild type counterparts (p<0.0001). Thinning of the retina particularly involving inner retinal layers and reduction in axonal density in the optic nerve was also observed. TUNEL staining was performed to examine neuronal apoptosis in the inner retina. Intraocular pressure (IOP) measurements showed that APP-PS1ΔE9 mice had a slightly elevated IOP, but the significance of this finding is not yet known. Together, these results substantiate previous observations and highlight that APP-PS1ΔE9 mice show evidence of molecular, functional and morphological degenerative changes in the inner retina.

摘要

阿尔茨海默病(AD)的APP-PS1ΔE9小鼠模型由于突变的人类APP和PSEN1转基因的高表达,在其中枢神经系统中表现出随年龄增长的淀粉样β(Aβ)斑块形成。在这里,我们使用免疫荧光、视网膜平铺片和蛋白质印迹技术相结合的方法,评估了老年APP-PS1小鼠视网膜中Aβ的沉积以及可溶性Aβ积累的变化。先前已证明,在青光眼动物模型中,视网膜中的Aβ积累与视网膜神经节细胞凋亡有关。本研究分别使用电生理学和组织学方法,研究了APP-PS1小鼠视网膜内层功能和结构上的变化。我们首次报告,与野生型对照相比,转基因动物中代表视网膜内层功能的暗视阈值反应(STR)振幅显著下降(p<0.0001)。还观察到视网膜变薄,特别是涉及视网膜内层,以及视神经轴突密度降低。进行TUNEL染色以检查视网膜内层的神经元凋亡。眼内压(IOP)测量显示,APP-PS1ΔE9小鼠的IOP略有升高,但这一发现的意义尚不清楚。总之,这些结果证实了先前的观察结果,并突出表明APP-PS1ΔE9小鼠在视网膜内层显示出分子、功能和形态学退行性变化的证据。

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