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Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease

机译:Tg2576和APPswe / PS1dE9阿尔茨海默氏病转基因小鼠模型之间淀粉样β谱的杰出表型差异

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摘要

APPswe/PS1dE9 and Tg2576 are very common transgenic mouse models of Alzheimer’s disease (AD), used in many laboratories as tools to research the mechanistic process leading to the disease. In order to augment our knowledge about the amyloid-β (Aβ) isoforms present in both transgenic mouse models, we have developed two chromatographic methods, one acidic and the other basic, for the characterization of the Aβ species produced in the brains of the two transgenic mouse models. After immunoprecipitation and micro-liquid chromatography-electrospray ionization mass spectrometry/mass spectrometry, 10 species of Aβ, surprisingly all of human origin, were detected in the brain of Tg2576 mouse, whereas 39 species, of both murine and human origin, were detected in the brain of the APP/PS1 mouse. To the best of our knowledge, this is the first study showing the identification of such a high number of Aβ species in the brain of the APP/PS1 transgenic mouse, whereas, in contrast, a much lower number of Aβ species were identified in the Tg2576 mouse. Therefore, this study brings to light a relevant phenotypic difference between these two popular mice models of AD.
机译:APPswe / PS1dE9和Tg2576是阿尔茨海默氏病(AD)的非常常见的转基因小鼠模型,在许多实验室中用作研究导致该疾病的机理的工具。为了增加我们对两种转基因小鼠模型中存在的淀粉样β(Aβ)亚型的了解,我们开发了两种色谱方法,一种是酸性的,另一种是碱性的,用于表征两种大脑中产生的Aβ种类。转基因小鼠模型。经过免疫沉淀和微液相色谱-电喷雾电离质谱/质谱法,在Tg2576小鼠的大脑中检测到10种令人惊奇的全人类来源的Aβ,而在Tg2576小鼠的脑中检测到39种鼠和人来源的Aβ。 APP / PS1鼠标的大脑。据我们所知,这是第一项研究,表明在APP / PS1转基因小鼠的大脑中鉴定出如此大量的Aβ物种,而相比之下,在APP / PS1转基因小鼠中鉴定出的Aβ物种数量少得多。 TG2576鼠标。因此,本研究揭示了这两种流行的AD模型之间的相关表型差异。

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