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Alpha-synuclein mRNA expression in oligodendrocytes in MSA

Multiple system atrophy (MSA) is a progressive neurodegenerative disease presenting clinically with parkinsonian, cerebellar, and autonomic features. α-Synuclein (αsyn), encoded by the gene SNCA, is the main constituent of glial cytoplasmic inclusion (GCI) found in oligodendrocytes in MSA, but the m...

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Autores principales: Asi, Yasmine T, Simpson, Julie E, Heath, Paul R, Wharton, Stephen B, Lees, Andrew J, Revesz, Tamas, Houlden, Henry, Holton, Janice L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238782/
https://www.ncbi.nlm.nih.gov/pubmed/24590631
http://dx.doi.org/10.1002/glia.22653
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author Asi, Yasmine T
Simpson, Julie E
Heath, Paul R
Wharton, Stephen B
Lees, Andrew J
Revesz, Tamas
Houlden, Henry
Holton, Janice L
author_facet Asi, Yasmine T
Simpson, Julie E
Heath, Paul R
Wharton, Stephen B
Lees, Andrew J
Revesz, Tamas
Houlden, Henry
Holton, Janice L
author_sort Asi, Yasmine T
collection PubMed
description Multiple system atrophy (MSA) is a progressive neurodegenerative disease presenting clinically with parkinsonian, cerebellar, and autonomic features. α-Synuclein (αsyn), encoded by the gene SNCA, is the main constituent of glial cytoplasmic inclusion (GCI) found in oligodendrocytes in MSA, but the methods of its accumulation have not been established. The aim of this study is to investigate alterations in regional and cellular SNCA mRNA expression in MSA as a possible substrate for GCI formation. Quantitative reverse transcription polymerase chain reaction (qPCR) was performed on postmortem brain samples from 15 MSA, 5 IPD, and 5 control cases to investigate regional expression in the frontal and occipital regions, dorsal putamen, pontine base, and cerebellum. For cellular expression analysis, neurons and oligodendrocytes were isolated by laser-capture microdissection from five MSA and five control cases. SNCA mRNA expression was not significantly different between the MSA, IPD and control cases in all regions (multilevel model, P = 0.14). After adjusting for group effect, the highest expression was found in the occipital cortex while the lowest was in the putamen (multilevel model, P < 0.0001). At the cellular level, MSA oligodendrocytes expressed more SNCA than control oligodendrocytes and expression in MSA neurons was slightly lower than that in controls, however, these results did not reach statistical significance. We have demonstrated regional variations in SNCA expression, which is higher in cortical than subcortical regions. This study is the first to demonstrate SNCA mRNA expression by oligodendrocytes in human postmortem tissue using qPCR and, although not statistically significant, could suggest that this may be increased in MSA compared to controls.
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spelling pubmed-42387822014-11-28 Alpha-synuclein mRNA expression in oligodendrocytes in MSA Asi, Yasmine T Simpson, Julie E Heath, Paul R Wharton, Stephen B Lees, Andrew J Revesz, Tamas Houlden, Henry Holton, Janice L Glia Research Articles Multiple system atrophy (MSA) is a progressive neurodegenerative disease presenting clinically with parkinsonian, cerebellar, and autonomic features. α-Synuclein (αsyn), encoded by the gene SNCA, is the main constituent of glial cytoplasmic inclusion (GCI) found in oligodendrocytes in MSA, but the methods of its accumulation have not been established. The aim of this study is to investigate alterations in regional and cellular SNCA mRNA expression in MSA as a possible substrate for GCI formation. Quantitative reverse transcription polymerase chain reaction (qPCR) was performed on postmortem brain samples from 15 MSA, 5 IPD, and 5 control cases to investigate regional expression in the frontal and occipital regions, dorsal putamen, pontine base, and cerebellum. For cellular expression analysis, neurons and oligodendrocytes were isolated by laser-capture microdissection from five MSA and five control cases. SNCA mRNA expression was not significantly different between the MSA, IPD and control cases in all regions (multilevel model, P = 0.14). After adjusting for group effect, the highest expression was found in the occipital cortex while the lowest was in the putamen (multilevel model, P < 0.0001). At the cellular level, MSA oligodendrocytes expressed more SNCA than control oligodendrocytes and expression in MSA neurons was slightly lower than that in controls, however, these results did not reach statistical significance. We have demonstrated regional variations in SNCA expression, which is higher in cortical than subcortical regions. This study is the first to demonstrate SNCA mRNA expression by oligodendrocytes in human postmortem tissue using qPCR and, although not statistically significant, could suggest that this may be increased in MSA compared to controls. BlackWell Publishing Ltd 2014-06 2014-03-03 /pmc/articles/PMC4238782/ /pubmed/24590631 http://dx.doi.org/10.1002/glia.22653 Text en © 2014 The Authors. Glia Published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Asi, Yasmine T
Simpson, Julie E
Heath, Paul R
Wharton, Stephen B
Lees, Andrew J
Revesz, Tamas
Houlden, Henry
Holton, Janice L
Alpha-synuclein mRNA expression in oligodendrocytes in MSA
title Alpha-synuclein mRNA expression in oligodendrocytes in MSA
title_full Alpha-synuclein mRNA expression in oligodendrocytes in MSA
title_fullStr Alpha-synuclein mRNA expression in oligodendrocytes in MSA
title_full_unstemmed Alpha-synuclein mRNA expression in oligodendrocytes in MSA
title_short Alpha-synuclein mRNA expression in oligodendrocytes in MSA
title_sort alpha-synuclein mrna expression in oligodendrocytes in msa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238782/
https://www.ncbi.nlm.nih.gov/pubmed/24590631
http://dx.doi.org/10.1002/glia.22653
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