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Drosophila Models of Tauopathies: What Have We Learned?

Aggregates of the microtubule-associated protein Tau are neuropathological hallmark lesions in Alzheimer's disease (AD) and related primary tauopathies. In addition, Tau is genetically implicated in a number of human neurodegenerative disorders including frontotemporal dementia (FTD) and Parkin...

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Autores principales: Gistelinck, Marc, Lambert, Jean-Charles, Callaerts, Patrick, Dermaut, Bart, Dourlen, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3373119/
https://www.ncbi.nlm.nih.gov/pubmed/22701808
http://dx.doi.org/10.1155/2012/970980
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author Gistelinck, Marc
Lambert, Jean-Charles
Callaerts, Patrick
Dermaut, Bart
Dourlen, Pierre
author_facet Gistelinck, Marc
Lambert, Jean-Charles
Callaerts, Patrick
Dermaut, Bart
Dourlen, Pierre
author_sort Gistelinck, Marc
collection PubMed
description Aggregates of the microtubule-associated protein Tau are neuropathological hallmark lesions in Alzheimer's disease (AD) and related primary tauopathies. In addition, Tau is genetically implicated in a number of human neurodegenerative disorders including frontotemporal dementia (FTD) and Parkinson's disease (PD). The exact mechanism by which Tau exerts its neurotoxicity is incompletely understood. Here, we give an overview of how studies using the genetic model organism Drosophila over the past decade have contributed to the molecular understanding of Tau neurotoxicity. We compare the different available readouts for Tau neurotoxicity in flies and review the molecular pathways in which Tau has been implicated. Finally, we emphasize that the integration of genome-wide approaches in human or mice with high-throughput genetic validation in Drosophila is a fruitful approach.
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spelling pubmed-33731192012-06-14 Drosophila Models of Tauopathies: What Have We Learned? Gistelinck, Marc Lambert, Jean-Charles Callaerts, Patrick Dermaut, Bart Dourlen, Pierre Int J Alzheimers Dis Review Article Aggregates of the microtubule-associated protein Tau are neuropathological hallmark lesions in Alzheimer's disease (AD) and related primary tauopathies. In addition, Tau is genetically implicated in a number of human neurodegenerative disorders including frontotemporal dementia (FTD) and Parkinson's disease (PD). The exact mechanism by which Tau exerts its neurotoxicity is incompletely understood. Here, we give an overview of how studies using the genetic model organism Drosophila over the past decade have contributed to the molecular understanding of Tau neurotoxicity. We compare the different available readouts for Tau neurotoxicity in flies and review the molecular pathways in which Tau has been implicated. Finally, we emphasize that the integration of genome-wide approaches in human or mice with high-throughput genetic validation in Drosophila is a fruitful approach. Hindawi Publishing Corporation 2012 2012-06-04 /pmc/articles/PMC3373119/ /pubmed/22701808 http://dx.doi.org/10.1155/2012/970980 Text en Copyright © 2012 Marc Gistelinck et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gistelinck, Marc
Lambert, Jean-Charles
Callaerts, Patrick
Dermaut, Bart
Dourlen, Pierre
Drosophila Models of Tauopathies: What Have We Learned?
title Drosophila Models of Tauopathies: What Have We Learned?
title_full Drosophila Models of Tauopathies: What Have We Learned?
title_fullStr Drosophila Models of Tauopathies: What Have We Learned?
title_full_unstemmed Drosophila Models of Tauopathies: What Have We Learned?
title_short Drosophila Models of Tauopathies: What Have We Learned?
title_sort drosophila models of tauopathies: what have we learned?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3373119/
https://www.ncbi.nlm.nih.gov/pubmed/22701808
http://dx.doi.org/10.1155/2012/970980
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