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Utilization of APPswe/PS1dE9 Transgenic Mice in Research of Alzheimer's Disease: Focus on Gene Therapy and Cell-Based Therapy Applications

机译:APPswe / PS1dE9转基因小鼠在阿尔茨海默氏病研究中的应用:专注于基因治疗和基于细胞的治疗应用

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摘要

One of the most extensively used transgenic mouse model of Alzheimer's disease (AD) is APPswe/PS1dE9 mice, which over express the Swedish mutation of APP together with PS1 deleted in exon 9. These mice show increase in parenchymal Aβ load with Aβ plaques starting from the age of four months, glial activation, and deficits in cognitive functions at the age of 6 months demonstrated by radial arm water maze and 12-13 months seen with Morris Water Maze test. As gene transfer technology allows the delivery of DNA into target cells to achieve the expression of a protective or therapeutic protein, and stem cell transplantation may create an environment supporting neuronal functions and clearing Aβ plaques, these therapeutic approaches alone or in combination represent potential therapeutic strategies that need to be tested in relevant animal models before testing in clinics. Here we review the current utilization of APPswe/PS1dE9 mice in testing gene transfer and cell transplantation aimed at improving the protection of the neurons against Aβ toxicity and also reducing the brain levels of Aβ. Both gene therapy and cell based therapy may be feasible therapeutic approaches for human AD.
机译:APPswe / PS1dE9小鼠是阿尔茨海默氏病(AD)用途最广泛的转基因小鼠模型之一,可过表达APP的瑞典突变以及外显子9中缺失的PS1。这些小鼠表现出实质性Aβ负荷增加,Aβ斑块始于radial臂水迷宫和Morris水迷宫测试显示12个月时,显示了4个月大,神经胶质活化和6个月时认知功能缺陷。由于基因转移技术允许将DNA传递到靶细胞中以实现保护性或治疗性蛋白的表达,并且干细胞移植可以创造一个支持神经元功能和清除Aβ斑块的环境,这些治疗方法单独或组合使用均代表了潜在的治疗策略在临床测试之前,需要先在相关动物模型中进行测试。在这里,我们审查了APPswe / PS1dE9小鼠在测试基因转移和细胞移植中的当前用途,目的是改善神经元对Aβ毒性的保护并降低Aβ的大脑水平。基因疗法和基于细胞的疗法都可能是人类AD的可行治疗方法。

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