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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. | LitMetric

AI Article Synopsis

  • The study investigates amyloid-β (Aβ) isoforms in two common transgenic mouse models of Alzheimer's disease, APPswe/PS1dE9 and Tg2576, highlighting their usefulness in researching disease mechanisms.
  • Two chromatographic methods were developed to analyze Aβ species from the brains of these mice, revealing that the Tg2576 model had 10 Aβ species, all of human origin, while the APP/PS1 model had 39 species from both human and murine origins.
  • This research is significant as it identifies a notable phenotypic difference between the two models, with a previously unreported high number of Aβ species found in the APP/PS1 transgenic mouse.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981901PMC
http://dx.doi.org/10.3233/JAD-160280DOI Listing

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