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Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models

Transgenic mouse models represent an essential tool for the exploration of Alzheimer’s disease (AD) pathological mechanisms and the development of novel treatments, which at present provide only symptomatic and transient effects. While a variety of mouse models successfully reflects the main neuropa...

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Detalles Bibliográficos
Autores principales: Wirths, Oliver, Zampar, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663280/
https://www.ncbi.nlm.nih.gov/pubmed/33143374
http://dx.doi.org/10.3390/ijms21218144
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author Wirths, Oliver
Zampar, Silvia
author_facet Wirths, Oliver
Zampar, Silvia
author_sort Wirths, Oliver
collection PubMed
description Transgenic mouse models represent an essential tool for the exploration of Alzheimer’s disease (AD) pathological mechanisms and the development of novel treatments, which at present provide only symptomatic and transient effects. While a variety of mouse models successfully reflects the main neuropathological hallmarks of AD, such as extracellular amyloid-β (Aβ) deposits, intracellular accumulation of Tau protein, the development of micro- and astrogliosis, as well as behavioral deficits, substantial neuron loss, as a key feature of the disease, seems to be more difficult to achieve. In this review, we summarize information on classic and more recent transgenic mouse models for AD, focusing in particular on loss of pyramidal, inter-, and cholinergic neurons. Although the cause of neuron loss in AD is still a matter of scientific debate, it seems to be linked to intraneuronal Aβ accumulation in several transgenic mouse models, especially in pyramidal neurons.
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spelling pubmed-76632802020-11-14 Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models Wirths, Oliver Zampar, Silvia Int J Mol Sci Review Transgenic mouse models represent an essential tool for the exploration of Alzheimer’s disease (AD) pathological mechanisms and the development of novel treatments, which at present provide only symptomatic and transient effects. While a variety of mouse models successfully reflects the main neuropathological hallmarks of AD, such as extracellular amyloid-β (Aβ) deposits, intracellular accumulation of Tau protein, the development of micro- and astrogliosis, as well as behavioral deficits, substantial neuron loss, as a key feature of the disease, seems to be more difficult to achieve. In this review, we summarize information on classic and more recent transgenic mouse models for AD, focusing in particular on loss of pyramidal, inter-, and cholinergic neurons. Although the cause of neuron loss in AD is still a matter of scientific debate, it seems to be linked to intraneuronal Aβ accumulation in several transgenic mouse models, especially in pyramidal neurons. MDPI 2020-10-30 /pmc/articles/PMC7663280/ /pubmed/33143374 http://dx.doi.org/10.3390/ijms21218144 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wirths, Oliver
Zampar, Silvia
Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models
title Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models
title_full Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models
title_fullStr Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models
title_full_unstemmed Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models
title_short Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models
title_sort neuron loss in alzheimer’s disease: translation in transgenic mouse models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663280/
https://www.ncbi.nlm.nih.gov/pubmed/33143374
http://dx.doi.org/10.3390/ijms21218144
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