An evaluation of Drosophila as a model system for studying tauopathies such as Alzheimer's disease
An evaluation of Drosophila as a model system for studying tauopathies such as Alzheimer's disease
Work spanning almost two decades using the fruit fly, Drosophila melanogaster, to study tau-mediated neurodegeneration has provided valuable and novel insights into the causes and mechanisms of tau-mediated toxicity and dysfunction in tauopathies such as Alzheimer's disease (AD). The fly has proven to be an excellent model for human diseases because of its cost efficiency, and the availability of powerful genetic tools for use in a comparatively less-complicated, but evolutionarily conserved, in vivo system. In this review, we provide a critical evaluation of the insights provided by fly models, highlighting both the advantages and limitations of the system. The fly has contributed to a greater understanding of the causes of tau abnormalities, the role of these abnormalities in mediating toxicity and/or dysfunction, and the nature of causative species mediating tau-toxicity. However, it is not possible to perfectly model all aspects of human degenerative diseases. What sets the fly apart from other animal models is its genetic tractability, which makes it highly amenable to overcoming experimental limitations. The explosion of genetic technology since the first fly disease models were established has translated into fly lines that allow for greater temporal control in restricting tau expression to single neuron types, and lines that can label and monitor the function of subcellular structures and components; thus, fly models offer an unprecedented view of the neurodegenerative process. Emerging genetic technology means that the fly provides an ever-evolving experimental platform for studying disease.
Alzheimer's disease, Animal models, Drosophila, Neurodegenerative diseases, Tauopathy
77-88
Sivanantharajah, Lovesha
b8424598-bb51-4049-a795-99e318c5b598
Mudher, Amritpal
ce0ccb35-ac49-4b6c-92b4-8dd5e78ac119
Shepherd, David
11aa6858-d19c-4450-82ff-11dff9dcd9c4
1 May 2019
Sivanantharajah, Lovesha
b8424598-bb51-4049-a795-99e318c5b598
Mudher, Amritpal
ce0ccb35-ac49-4b6c-92b4-8dd5e78ac119
Shepherd, David
11aa6858-d19c-4450-82ff-11dff9dcd9c4
Sivanantharajah, Lovesha, Mudher, Amritpal and Shepherd, David
(2019)
An evaluation of Drosophila as a model system for studying tauopathies such as Alzheimer's disease.
Journal of Neuroscience Methods, 319, .
(doi:10.1016/j.jneumeth.2019.01.001).
Abstract
Work spanning almost two decades using the fruit fly, Drosophila melanogaster, to study tau-mediated neurodegeneration has provided valuable and novel insights into the causes and mechanisms of tau-mediated toxicity and dysfunction in tauopathies such as Alzheimer's disease (AD). The fly has proven to be an excellent model for human diseases because of its cost efficiency, and the availability of powerful genetic tools for use in a comparatively less-complicated, but evolutionarily conserved, in vivo system. In this review, we provide a critical evaluation of the insights provided by fly models, highlighting both the advantages and limitations of the system. The fly has contributed to a greater understanding of the causes of tau abnormalities, the role of these abnormalities in mediating toxicity and/or dysfunction, and the nature of causative species mediating tau-toxicity. However, it is not possible to perfectly model all aspects of human degenerative diseases. What sets the fly apart from other animal models is its genetic tractability, which makes it highly amenable to overcoming experimental limitations. The explosion of genetic technology since the first fly disease models were established has translated into fly lines that allow for greater temporal control in restricting tau expression to single neuron types, and lines that can label and monitor the function of subcellular structures and components; thus, fly models offer an unprecedented view of the neurodegenerative process. Emerging genetic technology means that the fly provides an ever-evolving experimental platform for studying disease.
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Accepted/In Press date: 7 January 2019
e-pub ahead of print date: 8 January 2019
Published date: 1 May 2019
Keywords:
Alzheimer's disease, Animal models, Drosophila, Neurodegenerative diseases, Tauopathy
Identifiers
Local EPrints ID: 429896
URI: http://eprints.soton.ac.uk/id/eprint/429896
ISSN: 0165-0270
PURE UUID: 2cd94674-d8f2-4382-b507-1ac1662e75ee
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Date deposited: 08 Apr 2019 16:30
Last modified: 06 Aug 2024 01:52
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Author:
Lovesha Sivanantharajah
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