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Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease

Flies expressing the most common Parkinson disease (PD)-related mutation, LRRK2-G2019S, in their dopaminergic neurons show loss of visual function and degeneration of the retina, including mitochondrial abnormalities, apoptosis and autophagy. Since the photoreceptors that degenerate are not dopamine...

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Autores principales: Hindle, Samantha J., Elliott, Christopher J.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672307/
https://www.ncbi.nlm.nih.gov/pubmed/23529190
http://dx.doi.org/10.4161/auto.24397
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author Hindle, Samantha J.
Elliott, Christopher J.H.
author_facet Hindle, Samantha J.
Elliott, Christopher J.H.
author_sort Hindle, Samantha J.
collection PubMed
description Flies expressing the most common Parkinson disease (PD)-related mutation, LRRK2-G2019S, in their dopaminergic neurons show loss of visual function and degeneration of the retina, including mitochondrial abnormalities, apoptosis and autophagy. Since the photoreceptors that degenerate are not dopaminergic, this demonstrates nonautonomous degeneration, and a spread of pathology. This provides a model consistent with Braak’s hypothesis on progressive PD. The loss of visual function is specific for the G2019S mutation, implying the cause is its increased kinase activity, and is enhanced by increased neuronal activity. These data suggest novel explanations for the variability in animal models of PD. The specificity of visual loss to G2019S, coupled with the differences in neural firing rate, provide an explanation for the variability between people with PD in visual tests.
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spelling pubmed-36723072013-06-27 Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease Hindle, Samantha J. Elliott, Christopher J.H. Autophagy Autophagic Punctum Flies expressing the most common Parkinson disease (PD)-related mutation, LRRK2-G2019S, in their dopaminergic neurons show loss of visual function and degeneration of the retina, including mitochondrial abnormalities, apoptosis and autophagy. Since the photoreceptors that degenerate are not dopaminergic, this demonstrates nonautonomous degeneration, and a spread of pathology. This provides a model consistent with Braak’s hypothesis on progressive PD. The loss of visual function is specific for the G2019S mutation, implying the cause is its increased kinase activity, and is enhanced by increased neuronal activity. These data suggest novel explanations for the variability in animal models of PD. The specificity of visual loss to G2019S, coupled with the differences in neural firing rate, provide an explanation for the variability between people with PD in visual tests. Landes Bioscience 2013-06-01 2013-03-25 /pmc/articles/PMC3672307/ /pubmed/23529190 http://dx.doi.org/10.4161/auto.24397 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Autophagic Punctum
Hindle, Samantha J.
Elliott, Christopher J.H.
Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease
title Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease
title_full Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease
title_fullStr Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease
title_full_unstemmed Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease
title_short Spread of neuronal degeneration in a dopaminergic, Lrrk-G2019S model of Parkinson disease
title_sort spread of neuronal degeneration in a dopaminergic, lrrk-g2019s model of parkinson disease
topic Autophagic Punctum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672307/
https://www.ncbi.nlm.nih.gov/pubmed/23529190
http://dx.doi.org/10.4161/auto.24397
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