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阿尔茨海默病转基因小鼠的构建及鉴定

Establishment and Identification of Alzheimer Disease Transgenic Mouse Model

  • 摘要: 阿尔茨海默病(Alzheimer disease, AD)是一种病因不明的原发性脑部神经系统疾病,多以老年斑和神经纤维缠结为特征,已严重威胁人类健康。建立理想的AD动物模型,对研究AD的发病机制以及药物筛选防治AD新药至关重要。将β-淀粉样前体蛋白(β-amyloid precursor protein,APP)基因整合到C57BL/6J小鼠(Mus musculus)基因组中,20周后取小鼠海马区。蛋白免疫沉淀和免疫组化检测结果显示有淀粉样前体蛋白表达;Y迷宫检测结果显示转基因小鼠记忆力变差,与空白对照组比较下降了18%。阿尔茨海默病转基因小鼠动物模型的成功构建,为进一步研究AD疾病提供了良好的研究基础。

     

    Abstract: Alzheimer disease(AD) is a type of primary brain neurological disease with unknown etiology. It is characterized by senile plaques and nerve fiber tangles, and has been a serious threat to human health. The establishment of an ideal animal model of AD, to research on AD pathogenesis, AD screening and prevention of new drugs is essential. β-amyloid precursor protein(APP) gene was integrated into the C57 BL/6 J mice(Mus musculus) genome, and the hippocampus of mice were taken after twenty weeks. immunoprecipitation and immunohistochemical results showed amyloid precursor protein expression, Y maze detection result showed transgenic mice got worse memory, and decreased by 18% compared with the blank control group. The establishment of Alzheimer disease transgenic mouse model provides a good foundation to further AD disease research.

     

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