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Neurophysiology of Drosophila Models of Parkinson's Disease
We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson's disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Given the neurological impact of disease causing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414211/ https://www.ncbi.nlm.nih.gov/pubmed/25960916 http://dx.doi.org/10.1155/2015/381281 |
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author | West, Ryan J. H. Furmston, Rebecca Williams, Charles A. C. Elliott, Christopher J. H. |
author_facet | West, Ryan J. H. Furmston, Rebecca Williams, Charles A. C. Elliott, Christopher J. H. |
author_sort | West, Ryan J. H. |
collection | PubMed |
description | We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson's disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Given the neurological impact of disease causing mutations within these same genes in humans the phenotypes observed in fly are of significant interest. As such we observe four unique opportunities provided by fly nervous system models of Parkinson's disease. Firstly, Drosophila models are instrumental in exploring the mechanisms of neurodegeneration, with several PD-related mutations eliciting related phenotypes including sensitivity to energy supply and vesicular deformities. These are leading to the identification of plausible cellular mechanisms, which may be specific to (dopaminergic) neurons and synapses rather than general cellular phenotypes. Secondly, models show noncell autonomous signalling within the nervous system, offering the opportunity to develop our understanding of the way pathogenic signalling propagates, resembling Braak's scheme of spreading pathology in PD. Thirdly, the models link physiological deficits to changes in synaptic structure. While the structure-function relationship is complex, the genetic tractability of Drosophila offers the chance to separate fundamental changes from downstream consequences. Finally, the strong neuronal phenotypes permit relevant first in vivo drug testing. |
format | Online Article Text |
id | pubmed-4414211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-44142112015-05-10 Neurophysiology of Drosophila Models of Parkinson's Disease West, Ryan J. H. Furmston, Rebecca Williams, Charles A. C. Elliott, Christopher J. H. Parkinsons Dis Review Article We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson's disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Given the neurological impact of disease causing mutations within these same genes in humans the phenotypes observed in fly are of significant interest. As such we observe four unique opportunities provided by fly nervous system models of Parkinson's disease. Firstly, Drosophila models are instrumental in exploring the mechanisms of neurodegeneration, with several PD-related mutations eliciting related phenotypes including sensitivity to energy supply and vesicular deformities. These are leading to the identification of plausible cellular mechanisms, which may be specific to (dopaminergic) neurons and synapses rather than general cellular phenotypes. Secondly, models show noncell autonomous signalling within the nervous system, offering the opportunity to develop our understanding of the way pathogenic signalling propagates, resembling Braak's scheme of spreading pathology in PD. Thirdly, the models link physiological deficits to changes in synaptic structure. While the structure-function relationship is complex, the genetic tractability of Drosophila offers the chance to separate fundamental changes from downstream consequences. Finally, the strong neuronal phenotypes permit relevant first in vivo drug testing. Hindawi Publishing Corporation 2015 2015-04-20 /pmc/articles/PMC4414211/ /pubmed/25960916 http://dx.doi.org/10.1155/2015/381281 Text en Copyright © 2015 Ryan J. H. West 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 West, Ryan J. H. Furmston, Rebecca Williams, Charles A. C. Elliott, Christopher J. H. Neurophysiology of Drosophila Models of Parkinson's Disease |
title | Neurophysiology of Drosophila Models of Parkinson's Disease |
title_full | Neurophysiology of Drosophila Models of Parkinson's Disease |
title_fullStr | Neurophysiology of Drosophila Models of Parkinson's Disease |
title_full_unstemmed | Neurophysiology of Drosophila Models of Parkinson's Disease |
title_short | Neurophysiology of Drosophila Models of Parkinson's Disease |
title_sort | neurophysiology of drosophila models of parkinson's disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414211/ https://www.ncbi.nlm.nih.gov/pubmed/25960916 http://dx.doi.org/10.1155/2015/381281 |
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