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MicroRNA dysregulation in multiple sclerosis
Multiple sclerosis (MS) is a chronic inflammatory disease characterized by central nervous system (CNS) demyelination and axonal degeneration. Although the cause of MS is still unknown, it is widely accepted that novel drug targets need to focus on both decreasing inflammation and promoting CNS repa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551282/ https://www.ncbi.nlm.nih.gov/pubmed/23346094 http://dx.doi.org/10.3389/fgene.2012.00311 |
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author | Jr, Omar de Faria Moore, Craig S. Kennedy, Timothy E. Antel, Jack P. Bar-Or, Amit Dhaunchak, Ajit S. |
author_facet | Jr, Omar de Faria Moore, Craig S. Kennedy, Timothy E. Antel, Jack P. Bar-Or, Amit Dhaunchak, Ajit S. |
author_sort | Jr, Omar de Faria |
collection | PubMed |
description | Multiple sclerosis (MS) is a chronic inflammatory disease characterized by central nervous system (CNS) demyelination and axonal degeneration. Although the cause of MS is still unknown, it is widely accepted that novel drug targets need to focus on both decreasing inflammation and promoting CNS repair. In MS and experimental autoimmune encephalomyelitis, non-coding small microRNAs (miRNAs) are dysregulated in the immune system and CNS. Since individual miRNAs are able to down-regulate multiple targeted mRNA transcripts, even minor changes in miRNA expression may lead to significant alterations in gene expression. Herein, we review miRNA signatures reported in CNS tissue and immune cells of MS patients and consider how altered miRNA expression may influence MS pathology. |
format | Online Article Text |
id | pubmed-3551282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35512822013-01-23 MicroRNA dysregulation in multiple sclerosis Jr, Omar de Faria Moore, Craig S. Kennedy, Timothy E. Antel, Jack P. Bar-Or, Amit Dhaunchak, Ajit S. Front Genet Genetics Multiple sclerosis (MS) is a chronic inflammatory disease characterized by central nervous system (CNS) demyelination and axonal degeneration. Although the cause of MS is still unknown, it is widely accepted that novel drug targets need to focus on both decreasing inflammation and promoting CNS repair. In MS and experimental autoimmune encephalomyelitis, non-coding small microRNAs (miRNAs) are dysregulated in the immune system and CNS. Since individual miRNAs are able to down-regulate multiple targeted mRNA transcripts, even minor changes in miRNA expression may lead to significant alterations in gene expression. Herein, we review miRNA signatures reported in CNS tissue and immune cells of MS patients and consider how altered miRNA expression may influence MS pathology. Frontiers Media S.A. 2013-01-22 /pmc/articles/PMC3551282/ /pubmed/23346094 http://dx.doi.org/10.3389/fgene.2012.00311 Text en Copyright © de Faria O, Moore, Kennedy, Antel, Bar-Or and Dhaunchak. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Genetics Jr, Omar de Faria Moore, Craig S. Kennedy, Timothy E. Antel, Jack P. Bar-Or, Amit Dhaunchak, Ajit S. MicroRNA dysregulation in multiple sclerosis |
title | MicroRNA dysregulation in multiple sclerosis |
title_full | MicroRNA dysregulation in multiple sclerosis |
title_fullStr | MicroRNA dysregulation in multiple sclerosis |
title_full_unstemmed | MicroRNA dysregulation in multiple sclerosis |
title_short | MicroRNA dysregulation in multiple sclerosis |
title_sort | microrna dysregulation in multiple sclerosis |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551282/ https://www.ncbi.nlm.nih.gov/pubmed/23346094 http://dx.doi.org/10.3389/fgene.2012.00311 |
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