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Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease
The molecular mechanisms underlying caudal-to-rostral progression of Lewy body pathology in Parkinson’s disease remain poorly understood. Here, we identified transcriptomic signatures across brain regions involved in Braak Lewy body stages in non-neurological adults from the Allen Human Brain Atlas....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058608/ https://www.ncbi.nlm.nih.gov/pubmed/32139796 http://dx.doi.org/10.1038/s42003-020-0804-9 |
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author | Keo, Arlin Mahfouz, Ahmed Ingrassia, Angela M. T. Meneboo, Jean-Pascal Villenet, Celine Mutez, Eugénie Comptdaer, Thomas Lelieveldt, Boudewijn P. F. Figeac, Martin Chartier-Harlin, Marie-Christine van de Berg, Wilma D. J. van Hilten, Jacobus J. Reinders, Marcel J. T. |
author_facet | Keo, Arlin Mahfouz, Ahmed Ingrassia, Angela M. T. Meneboo, Jean-Pascal Villenet, Celine Mutez, Eugénie Comptdaer, Thomas Lelieveldt, Boudewijn P. F. Figeac, Martin Chartier-Harlin, Marie-Christine van de Berg, Wilma D. J. van Hilten, Jacobus J. Reinders, Marcel J. T. |
author_sort | Keo, Arlin |
collection | PubMed |
description | The molecular mechanisms underlying caudal-to-rostral progression of Lewy body pathology in Parkinson’s disease remain poorly understood. Here, we identified transcriptomic signatures across brain regions involved in Braak Lewy body stages in non-neurological adults from the Allen Human Brain Atlas. Among the genes that are indicative of regional vulnerability, we found known genetic risk factors for Parkinson’s disease: SCARB2, ELOVL7, SH3GL2, SNCA, BAP1, and ZNF184. Results were confirmed in two datasets of non-neurological subjects, while in two datasets of Parkinson’s disease patients we found altered expression patterns. Co-expression analysis across vulnerable regions identified a module enriched for genes associated with dopamine synthesis and microglia, and another module related to the immune system, blood-oxygen transport, and endothelial cells. Both were highly expressed in regions involved in the preclinical stages of the disease. Finally, alterations in genes underlying these region-specific functions may contribute to the selective regional vulnerability in Parkinson’s disease brains. |
format | Online Article Text |
id | pubmed-7058608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70586082020-03-19 Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease Keo, Arlin Mahfouz, Ahmed Ingrassia, Angela M. T. Meneboo, Jean-Pascal Villenet, Celine Mutez, Eugénie Comptdaer, Thomas Lelieveldt, Boudewijn P. F. Figeac, Martin Chartier-Harlin, Marie-Christine van de Berg, Wilma D. J. van Hilten, Jacobus J. Reinders, Marcel J. T. Commun Biol Article The molecular mechanisms underlying caudal-to-rostral progression of Lewy body pathology in Parkinson’s disease remain poorly understood. Here, we identified transcriptomic signatures across brain regions involved in Braak Lewy body stages in non-neurological adults from the Allen Human Brain Atlas. Among the genes that are indicative of regional vulnerability, we found known genetic risk factors for Parkinson’s disease: SCARB2, ELOVL7, SH3GL2, SNCA, BAP1, and ZNF184. Results were confirmed in two datasets of non-neurological subjects, while in two datasets of Parkinson’s disease patients we found altered expression patterns. Co-expression analysis across vulnerable regions identified a module enriched for genes associated with dopamine synthesis and microglia, and another module related to the immune system, blood-oxygen transport, and endothelial cells. Both were highly expressed in regions involved in the preclinical stages of the disease. Finally, alterations in genes underlying these region-specific functions may contribute to the selective regional vulnerability in Parkinson’s disease brains. Nature Publishing Group UK 2020-03-05 /pmc/articles/PMC7058608/ /pubmed/32139796 http://dx.doi.org/10.1038/s42003-020-0804-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Keo, Arlin Mahfouz, Ahmed Ingrassia, Angela M. T. Meneboo, Jean-Pascal Villenet, Celine Mutez, Eugénie Comptdaer, Thomas Lelieveldt, Boudewijn P. F. Figeac, Martin Chartier-Harlin, Marie-Christine van de Berg, Wilma D. J. van Hilten, Jacobus J. Reinders, Marcel J. T. Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease |
title | Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease |
title_full | Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease |
title_fullStr | Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease |
title_full_unstemmed | Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease |
title_short | Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease |
title_sort | transcriptomic signatures of brain regional vulnerability to parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058608/ https://www.ncbi.nlm.nih.gov/pubmed/32139796 http://dx.doi.org/10.1038/s42003-020-0804-9 |
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