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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

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...

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Autores principales: Allué, José Antonio, Sarasa, Leticia, Izco, María, Pérez-Grijalba, Virginia, Fandos, Noelia, Pascual-Lucas, María, Ogueta, Samuel, Pesini, Pedro, Sarasa, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981901/
https://www.ncbi.nlm.nih.gov/pubmed/27258422
http://dx.doi.org/10.3233/JAD-160280
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author Allué, José Antonio
Sarasa, Leticia
Izco, María
Pérez-Grijalba, Virginia
Fandos, Noelia
Pascual-Lucas, María
Ogueta, Samuel
Pesini, Pedro
Sarasa, Manuel
author_facet Allué, José Antonio
Sarasa, Leticia
Izco, María
Pérez-Grijalba, Virginia
Fandos, Noelia
Pascual-Lucas, María
Ogueta, Samuel
Pesini, Pedro
Sarasa, Manuel
author_sort Allué, José Antonio
collection PubMed
description 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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spelling pubmed-49819012016-08-16 Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease Allué, José Antonio Sarasa, Leticia Izco, María Pérez-Grijalba, Virginia Fandos, Noelia Pascual-Lucas, María Ogueta, Samuel Pesini, Pedro Sarasa, Manuel J Alzheimers Dis Research Article 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. IOS Press 2016-08-03 /pmc/articles/PMC4981901/ /pubmed/27258422 http://dx.doi.org/10.3233/JAD-160280 Text en IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Allué, José Antonio
Sarasa, Leticia
Izco, María
Pérez-Grijalba, Virginia
Fandos, Noelia
Pascual-Lucas, María
Ogueta, Samuel
Pesini, Pedro
Sarasa, Manuel
Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease
title Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease
title_full Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease
title_fullStr Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease
title_full_unstemmed Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease
title_short Outstanding Phenotypic Differences in the Profile of Amyloid-β between Tg2576 and APPswe/PS1dE9 Transgenic Mouse Models of Alzheimer’s Disease
title_sort outstanding phenotypic differences in the profile of amyloid-β between tg2576 and appswe/ps1de9 transgenic mouse models of alzheimer’s disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981901/
https://www.ncbi.nlm.nih.gov/pubmed/27258422
http://dx.doi.org/10.3233/JAD-160280
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