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Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease
Increasing evidence supports the role of brain and systemic inflammation in the etiology of Parkinson disease (PD). We used gene expression profiling to examine the activation state of peripheral blood monocytes in 18 patients with early, untreated PD and 16 healthy control (HC) subjects. Monocytes...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044127/ https://www.ncbi.nlm.nih.gov/pubmed/33850148 http://dx.doi.org/10.1038/s41531-021-00180-z |
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author | Carlisle, Samantha M. Qin, Hongwei Hendrickson, R. Curtis Muwanguzi, Jordana E. Lefkowitz, Elliot J. Kennedy, Richard E. Yan, Zhaoqi Yacoubian, Talene A. Benveniste, Etty N. West, Andrew B. Harms, Ashley S. Standaert, David G. |
author_facet | Carlisle, Samantha M. Qin, Hongwei Hendrickson, R. Curtis Muwanguzi, Jordana E. Lefkowitz, Elliot J. Kennedy, Richard E. Yan, Zhaoqi Yacoubian, Talene A. Benveniste, Etty N. West, Andrew B. Harms, Ashley S. Standaert, David G. |
author_sort | Carlisle, Samantha M. |
collection | PubMed |
description | Increasing evidence supports the role of brain and systemic inflammation in the etiology of Parkinson disease (PD). We used gene expression profiling to examine the activation state of peripheral blood monocytes in 18 patients with early, untreated PD and 16 healthy control (HC) subjects. Monocytes were isolated by negative selection, and gene expression studied by RNA-seq and gene set enrichment analysis. A computational model that incorporated case/control status, sex, and the interaction between case/control status and sex was utilized. We found that there was a striking effect of sex on monocyte gene expression. There was inflammatory activation of monocytes in females with PD, with enrichment of gene sets associated with interferon gamma stimulation. In males, the activation patterns were more heterogeneous. These data point to the importance of systemic monocyte activation in PD, and the importance of studies which examine the differential effects of sex on pathophysiology of the disease. |
format | Online Article Text |
id | pubmed-8044127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80441272021-04-28 Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease Carlisle, Samantha M. Qin, Hongwei Hendrickson, R. Curtis Muwanguzi, Jordana E. Lefkowitz, Elliot J. Kennedy, Richard E. Yan, Zhaoqi Yacoubian, Talene A. Benveniste, Etty N. West, Andrew B. Harms, Ashley S. Standaert, David G. NPJ Parkinsons Dis Article Increasing evidence supports the role of brain and systemic inflammation in the etiology of Parkinson disease (PD). We used gene expression profiling to examine the activation state of peripheral blood monocytes in 18 patients with early, untreated PD and 16 healthy control (HC) subjects. Monocytes were isolated by negative selection, and gene expression studied by RNA-seq and gene set enrichment analysis. A computational model that incorporated case/control status, sex, and the interaction between case/control status and sex was utilized. We found that there was a striking effect of sex on monocyte gene expression. There was inflammatory activation of monocytes in females with PD, with enrichment of gene sets associated with interferon gamma stimulation. In males, the activation patterns were more heterogeneous. These data point to the importance of systemic monocyte activation in PD, and the importance of studies which examine the differential effects of sex on pathophysiology of the disease. Nature Publishing Group UK 2021-04-13 /pmc/articles/PMC8044127/ /pubmed/33850148 http://dx.doi.org/10.1038/s41531-021-00180-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Carlisle, Samantha M. Qin, Hongwei Hendrickson, R. Curtis Muwanguzi, Jordana E. Lefkowitz, Elliot J. Kennedy, Richard E. Yan, Zhaoqi Yacoubian, Talene A. Benveniste, Etty N. West, Andrew B. Harms, Ashley S. Standaert, David G. Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease |
title | Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease |
title_full | Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease |
title_fullStr | Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease |
title_full_unstemmed | Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease |
title_short | Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease |
title_sort | sex-based differences in the activation of peripheral blood monocytes in early parkinson disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044127/ https://www.ncbi.nlm.nih.gov/pubmed/33850148 http://dx.doi.org/10.1038/s41531-021-00180-z |
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