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The domestic cat as a natural animal model of Alzheimer’s disease

INTRODUCTION: Alzheimer’s disease (AD) is the most dominant neurodegenerative disorder that causes dementia, and no effective treatments are available. To study its pathogenesis and develop therapeutics, animal models representing its pathologies are needed. Although many animal species develop seni...

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Autores principales: Chambers, James K., Tokuda, Takahiko, Uchida, Kazuyuki, Ishii, Ryotaro, Tatebe, Harutsugu, Takahashi, Erika, Tomiyama, Takami, Une, Yumi, Nakayama, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674944/
https://www.ncbi.nlm.nih.gov/pubmed/26651821
http://dx.doi.org/10.1186/s40478-015-0258-3
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author Chambers, James K.
Tokuda, Takahiko
Uchida, Kazuyuki
Ishii, Ryotaro
Tatebe, Harutsugu
Takahashi, Erika
Tomiyama, Takami
Une, Yumi
Nakayama, Hiroyuki
author_facet Chambers, James K.
Tokuda, Takahiko
Uchida, Kazuyuki
Ishii, Ryotaro
Tatebe, Harutsugu
Takahashi, Erika
Tomiyama, Takami
Une, Yumi
Nakayama, Hiroyuki
author_sort Chambers, James K.
collection PubMed
description INTRODUCTION: Alzheimer’s disease (AD) is the most dominant neurodegenerative disorder that causes dementia, and no effective treatments are available. To study its pathogenesis and develop therapeutics, animal models representing its pathologies are needed. Although many animal species develop senile plaques (SP) composed of amyloid-β (Aβ) proteins that are identical to those found in humans, none of them exhibit neurofibrillary tangles (NFT) and subsequent neurodegeneration, which are integral parts of the pathology of AD. RESULTS: The present study shows that Aβ accumulation, NFT formation, and significant neuronal loss all emerge naturally in the hippocampi of aged domestic cats. The NFT that form in the cat brain are identical to those seen in human AD in terms of their spatial distribution, the cells they affect, and the tau isoforms that comprise them. Interestingly, aged cats do not develop mature argyrophilic SP, but instead accumulate intraneuronal Aβ oligomers in their hippocampal pyramidal cells, which might be due to the amino acid sequence of felid Aβ. CONCLUSIONS: These results suggest that Aβ oligomers are more important than SP for NFT formation and the subsequent neurodegeneration. The domestic cat is a unique animal species that naturally replicates various AD pathologies, especially Aβ oligomer accumulation, NFT formation, and neuronal loss. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-015-0258-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-46749442015-12-11 The domestic cat as a natural animal model of Alzheimer’s disease Chambers, James K. Tokuda, Takahiko Uchida, Kazuyuki Ishii, Ryotaro Tatebe, Harutsugu Takahashi, Erika Tomiyama, Takami Une, Yumi Nakayama, Hiroyuki Acta Neuropathol Commun Research INTRODUCTION: Alzheimer’s disease (AD) is the most dominant neurodegenerative disorder that causes dementia, and no effective treatments are available. To study its pathogenesis and develop therapeutics, animal models representing its pathologies are needed. Although many animal species develop senile plaques (SP) composed of amyloid-β (Aβ) proteins that are identical to those found in humans, none of them exhibit neurofibrillary tangles (NFT) and subsequent neurodegeneration, which are integral parts of the pathology of AD. RESULTS: The present study shows that Aβ accumulation, NFT formation, and significant neuronal loss all emerge naturally in the hippocampi of aged domestic cats. The NFT that form in the cat brain are identical to those seen in human AD in terms of their spatial distribution, the cells they affect, and the tau isoforms that comprise them. Interestingly, aged cats do not develop mature argyrophilic SP, but instead accumulate intraneuronal Aβ oligomers in their hippocampal pyramidal cells, which might be due to the amino acid sequence of felid Aβ. CONCLUSIONS: These results suggest that Aβ oligomers are more important than SP for NFT formation and the subsequent neurodegeneration. The domestic cat is a unique animal species that naturally replicates various AD pathologies, especially Aβ oligomer accumulation, NFT formation, and neuronal loss. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-015-0258-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-10 /pmc/articles/PMC4674944/ /pubmed/26651821 http://dx.doi.org/10.1186/s40478-015-0258-3 Text en © Chambers et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chambers, James K.
Tokuda, Takahiko
Uchida, Kazuyuki
Ishii, Ryotaro
Tatebe, Harutsugu
Takahashi, Erika
Tomiyama, Takami
Une, Yumi
Nakayama, Hiroyuki
The domestic cat as a natural animal model of Alzheimer’s disease
title The domestic cat as a natural animal model of Alzheimer’s disease
title_full The domestic cat as a natural animal model of Alzheimer’s disease
title_fullStr The domestic cat as a natural animal model of Alzheimer’s disease
title_full_unstemmed The domestic cat as a natural animal model of Alzheimer’s disease
title_short The domestic cat as a natural animal model of Alzheimer’s disease
title_sort domestic cat as a natural animal model of alzheimer’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674944/
https://www.ncbi.nlm.nih.gov/pubmed/26651821
http://dx.doi.org/10.1186/s40478-015-0258-3
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