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Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate
Since age-dependent deposition of Aβ-amyloid has been reported in the Microcebus murinus, we posited that this animal could as well be a model of age-related synucleinopathy. We characterized the distribution of Aβ-amyloid, α-synuclein and two of its modified forms in the brain of Microcebus murinus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510464/ https://www.ncbi.nlm.nih.gov/pubmed/23205271 http://dx.doi.org/10.1038/srep00910 |
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author | Canron, Marie-Hélène Perret, Martine Vital, Anne Bézard, Erwan Dehay, Benjamin |
author_facet | Canron, Marie-Hélène Perret, Martine Vital, Anne Bézard, Erwan Dehay, Benjamin |
author_sort | Canron, Marie-Hélène |
collection | PubMed |
description | Since age-dependent deposition of Aβ-amyloid has been reported in the Microcebus murinus, we posited that this animal could as well be a model of age-related synucleinopathy. We characterized the distribution of Aβ-amyloid, α-synuclein and two of its modified forms in the brain of Microcebus murinus aged from 1.5 to 10 years. Intracytoplasmic α-synuclein aggregates were observed only in aged animals in different brain regions, which were also phospho-Ser129 and nitrated α-synuclein immunoreactive. Age-dependent α-synuclein aggregation occurs spontaneously in mouse lemur primates. Microcebus murinus may provide a model to study age-associated α-synucleinopathy and for testing putative therapeutic interventions for both Alzheimer's and Parkinson's diseases. |
format | Online Article Text |
id | pubmed-3510464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-35104642012-11-30 Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate Canron, Marie-Hélène Perret, Martine Vital, Anne Bézard, Erwan Dehay, Benjamin Sci Rep Article Since age-dependent deposition of Aβ-amyloid has been reported in the Microcebus murinus, we posited that this animal could as well be a model of age-related synucleinopathy. We characterized the distribution of Aβ-amyloid, α-synuclein and two of its modified forms in the brain of Microcebus murinus aged from 1.5 to 10 years. Intracytoplasmic α-synuclein aggregates were observed only in aged animals in different brain regions, which were also phospho-Ser129 and nitrated α-synuclein immunoreactive. Age-dependent α-synuclein aggregation occurs spontaneously in mouse lemur primates. Microcebus murinus may provide a model to study age-associated α-synucleinopathy and for testing putative therapeutic interventions for both Alzheimer's and Parkinson's diseases. Nature Publishing Group 2012-11-30 /pmc/articles/PMC3510464/ /pubmed/23205271 http://dx.doi.org/10.1038/srep00910 Text en Copyright © 2012, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Canron, Marie-Hélène Perret, Martine Vital, Anne Bézard, Erwan Dehay, Benjamin Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate |
title | Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate |
title_full | Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate |
title_fullStr | Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate |
title_full_unstemmed | Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate |
title_short | Age-dependent α-synuclein aggregation in the Microcebus murinus lemur primate |
title_sort | age-dependent α-synuclein aggregation in the microcebus murinus lemur primate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510464/ https://www.ncbi.nlm.nih.gov/pubmed/23205271 http://dx.doi.org/10.1038/srep00910 |
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