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Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis
Multiple sclerosis (MS) is an autoimmune, neurodegenerative disease but the molecular mechanisms underlying neurodegenerative aspects of the disease are poorly understood. microRNAs (miRNAs) are powerful regulators of gene expression that regulate numerous mRNAs simultaneously and can thus regulate...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128870/ https://www.ncbi.nlm.nih.gov/pubmed/30194392 http://dx.doi.org/10.1038/s41598-018-31542-y |
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author | Juźwik, Camille A. Drake, Sienna Lécuyer, Marc-André Johnson, Radia Marie Morquette, Barbara Zhang, Yang Charabati, Marc Sagan, Selena M. Bar-Or, Amit Prat, Alexandre Fournier, Alyson E. |
author_facet | Juźwik, Camille A. Drake, Sienna Lécuyer, Marc-André Johnson, Radia Marie Morquette, Barbara Zhang, Yang Charabati, Marc Sagan, Selena M. Bar-Or, Amit Prat, Alexandre Fournier, Alyson E. |
author_sort | Juźwik, Camille A. |
collection | PubMed |
description | Multiple sclerosis (MS) is an autoimmune, neurodegenerative disease but the molecular mechanisms underlying neurodegenerative aspects of the disease are poorly understood. microRNAs (miRNAs) are powerful regulators of gene expression that regulate numerous mRNAs simultaneously and can thus regulate programs of gene expression. Here, we describe miRNA expression in neurons captured from mice subjected to experimental autoimmune encephalomyelitis (EAE), a model of central nervous system (CNS) inflammation. Lumbar motor neurons and retinal neurons were laser captured from EAE mice and miRNA expression was assessed by next-generation sequencing and validated by qPCR. We describe 14 miRNAs that are differentially regulated in both neuronal subtypes and determine putative mRNA targets though in silico analysis. Several upregulated neuronal miRNAs are predicted to target pathways that could mediate repair and regeneration during EAE. This work identifies miRNAs that are affected by inflammation and suggests novel candidates that may be targeted to improve neuroprotection in the context of pathological inflammation. |
format | Online Article Text |
id | pubmed-6128870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61288702018-09-10 Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis Juźwik, Camille A. Drake, Sienna Lécuyer, Marc-André Johnson, Radia Marie Morquette, Barbara Zhang, Yang Charabati, Marc Sagan, Selena M. Bar-Or, Amit Prat, Alexandre Fournier, Alyson E. Sci Rep Article Multiple sclerosis (MS) is an autoimmune, neurodegenerative disease but the molecular mechanisms underlying neurodegenerative aspects of the disease are poorly understood. microRNAs (miRNAs) are powerful regulators of gene expression that regulate numerous mRNAs simultaneously and can thus regulate programs of gene expression. Here, we describe miRNA expression in neurons captured from mice subjected to experimental autoimmune encephalomyelitis (EAE), a model of central nervous system (CNS) inflammation. Lumbar motor neurons and retinal neurons were laser captured from EAE mice and miRNA expression was assessed by next-generation sequencing and validated by qPCR. We describe 14 miRNAs that are differentially regulated in both neuronal subtypes and determine putative mRNA targets though in silico analysis. Several upregulated neuronal miRNAs are predicted to target pathways that could mediate repair and regeneration during EAE. This work identifies miRNAs that are affected by inflammation and suggests novel candidates that may be targeted to improve neuroprotection in the context of pathological inflammation. Nature Publishing Group UK 2018-09-07 /pmc/articles/PMC6128870/ /pubmed/30194392 http://dx.doi.org/10.1038/s41598-018-31542-y Text en © The Author(s) 2018 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 Juźwik, Camille A. Drake, Sienna Lécuyer, Marc-André Johnson, Radia Marie Morquette, Barbara Zhang, Yang Charabati, Marc Sagan, Selena M. Bar-Or, Amit Prat, Alexandre Fournier, Alyson E. Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis |
title | Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis |
title_full | Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis |
title_fullStr | Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis |
title_full_unstemmed | Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis |
title_short | Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis |
title_sort | neuronal microrna regulation in experimental autoimmune encephalomyelitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128870/ https://www.ncbi.nlm.nih.gov/pubmed/30194392 http://dx.doi.org/10.1038/s41598-018-31542-y |
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