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A canine model of Alzheimer's disease generated by overexpressing a mutated human amyloid precursor protein

机译:通过过表达突变的人类淀粉样蛋白前体蛋白产生的阿尔茨海默氏病犬模型

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摘要

Canines are considered the most authentic model for studying multifactorial human diseases, as these animals typically share a common environment with man. Somatic cell nuclear transfer (SCNT) technology along with genetic engineering of nuclear donor cells provides a unique opportunity for examining human diseases using transgenic canines. In the present study, we generated transgenic canines that overexpressed the human amyloid precursor protein (APP) gene containing well-characterized familial Alzheimer's disease (AD) mutations. We successfully obtained five out of six live puppies by SCNT. This was confirmed by observing the expression of green fluorescence protein in the body as a visual transgenic marker and the overexpression of the mutated APP gene in the brain. The transgenic canines developed AD-like symptoms, such as enlarged ventricles, an atrophied hippocampus, and β-amyloid plaques in the brain. Thus, the transgenic canines we created can serve as a novel animal model for studying human AD.
机译:犬科动物被认为是研究人类多种疾病的最真实的模型,因为这些动物通常与人共享共同的环境。体细胞核移植(SCNT)技术以及核供体细胞的基因工程为使用转基因犬检查人类疾病提供了独特的机会。在当前的研究中,我们产生了过表达人淀粉样蛋白前体蛋白(APP)基因的转基因犬,该蛋白含有特征明确的家族性阿尔茨海默氏病(AD)突变。我们成功地从SCNT获得了六只活幼犬中的五只。通过观察绿色荧光蛋白作为可视转基因标记物在体内的表达以及突变的APP基因在脑中的过表达,可以证实这一点。转基因犬在大脑中出现AD样症状,例如脑室增大,海马萎缩和β-淀粉样斑块。因此,我们创建的转基因犬可以作为研究人类AD的新型动物模型。

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