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Rev-erbs and Glia—Implications for Neurodegenerative Diseases

Recently, we described a role for the circadian clock protein and nuclear receptor Rev-erbα in regulating glial activation states in the brain. Deletion of Rev-erbα resulted in microglial as well as astrocytic activation, while a Rev-erbα agonist diminished the severity of lipopolysaccharide (LPS)-i...

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Detalles Bibliográficos
Autores principales: Griffin, Percy, Dimitry, Julie M, Musiek, Erik S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552335/
https://www.ncbi.nlm.nih.gov/pubmed/31210735
http://dx.doi.org/10.1177/1179069519853233
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author Griffin, Percy
Dimitry, Julie M
Musiek, Erik S
author_facet Griffin, Percy
Dimitry, Julie M
Musiek, Erik S
author_sort Griffin, Percy
collection PubMed
description Recently, we described a role for the circadian clock protein and nuclear receptor Rev-erbα in regulating glial activation states in the brain. Deletion of Rev-erbα resulted in microglial as well as astrocytic activation, while a Rev-erbα agonist diminished the severity of lipopolysaccharide (LPS)-induced neuroinflammation. Concomitant with this glial activation is impaired neuronal health. These findings suggest that Rev-erb proteins may play critical roles in glial biology. Pertinent ideas such as the glial cell type of most importance, the translatability of these findings to human disease, and the effect of manipulating Rev-erbs in models of neurodegeneration, need to be explored further. In this commentary, we will address the potential role of Rev-erbs in neuroinflammation related to neurodegenerative diseases and speculate on Rev-erbs as potential therapeutic targets for these conditions.
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spelling pubmed-65523352019-06-17 Rev-erbs and Glia—Implications for Neurodegenerative Diseases Griffin, Percy Dimitry, Julie M Musiek, Erik S J Exp Neurosci Commentary Recently, we described a role for the circadian clock protein and nuclear receptor Rev-erbα in regulating glial activation states in the brain. Deletion of Rev-erbα resulted in microglial as well as astrocytic activation, while a Rev-erbα agonist diminished the severity of lipopolysaccharide (LPS)-induced neuroinflammation. Concomitant with this glial activation is impaired neuronal health. These findings suggest that Rev-erb proteins may play critical roles in glial biology. Pertinent ideas such as the glial cell type of most importance, the translatability of these findings to human disease, and the effect of manipulating Rev-erbs in models of neurodegeneration, need to be explored further. In this commentary, we will address the potential role of Rev-erbs in neuroinflammation related to neurodegenerative diseases and speculate on Rev-erbs as potential therapeutic targets for these conditions. SAGE Publications 2019-06-04 /pmc/articles/PMC6552335/ /pubmed/31210735 http://dx.doi.org/10.1177/1179069519853233 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Commentary
Griffin, Percy
Dimitry, Julie M
Musiek, Erik S
Rev-erbs and Glia—Implications for Neurodegenerative Diseases
title Rev-erbs and Glia—Implications for Neurodegenerative Diseases
title_full Rev-erbs and Glia—Implications for Neurodegenerative Diseases
title_fullStr Rev-erbs and Glia—Implications for Neurodegenerative Diseases
title_full_unstemmed Rev-erbs and Glia—Implications for Neurodegenerative Diseases
title_short Rev-erbs and Glia—Implications for Neurodegenerative Diseases
title_sort rev-erbs and glia—implications for neurodegenerative diseases
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552335/
https://www.ncbi.nlm.nih.gov/pubmed/31210735
http://dx.doi.org/10.1177/1179069519853233
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