MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis

MicroRNAs (miRNAs) are a recently discovered group of small noncoding RNAs that regulate gene expression post-transcriptionally. They are highly expressed in cells of the immune system, as well as in the central nervous system, and they are deregulated in various neurological disorders. Emerging evi...

Full description

Bibliographic Details
Main Authors: Fenoglio, Chiara, Ridolfi, Elisa, Galimberti, Daniela, Scarpini, Elio
Format: Online
Language:English
Published: Molecular Diversity Preservation International (MDPI) 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497323/
id pubmed-3497323
recordtype oai_dc
spelling pubmed-34973232012-11-29 MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis Fenoglio, Chiara Ridolfi, Elisa Galimberti, Daniela Scarpini, Elio Review MicroRNAs (miRNAs) are a recently discovered group of small noncoding RNAs that regulate gene expression post-transcriptionally. They are highly expressed in cells of the immune system, as well as in the central nervous system, and they are deregulated in various neurological disorders. Emerging evidence underlines an involvement of miRNAs in the pathogenesis of Multiple Sclerosis (MS). A number of miRNAs have been found to be dysregulated in blood cells from MS patients, in brain lesions, as well as in biological fluids such as serum and plasma. Despite miRNA altered expression likely showing a high tissue specificity, some profile similarities could be observed for certain miRNAs such as miR-326—such as upregulation in both active lesions and blood—though not for others such as miR-323, which demonstrated upregulation in whole blood, active brain lesions, and T-reg cells, but not in the serum of MS patients. In this review, the possible role of miRNAs in MS pathogenesis will be discussed according to all the available literature, with a particular emphasis on the possibility of considering extracellular miRNAs as a new source for both biomarker identification and therapeutic target discovery. Molecular Diversity Preservation International (MDPI) 2012-10-15 /pmc/articles/PMC3497323/ /pubmed/23202949 http://dx.doi.org/10.3390/ijms131013227 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0).
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Fenoglio, Chiara
Ridolfi, Elisa
Galimberti, Daniela
Scarpini, Elio
spellingShingle Fenoglio, Chiara
Ridolfi, Elisa
Galimberti, Daniela
Scarpini, Elio
MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis
author_facet Fenoglio, Chiara
Ridolfi, Elisa
Galimberti, Daniela
Scarpini, Elio
author_sort Fenoglio, Chiara
title MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis
title_short MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis
title_full MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis
title_fullStr MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis
title_full_unstemmed MicroRNAs as Active Players in the Pathogenesis of Multiple Sclerosis
title_sort micrornas as active players in the pathogenesis of multiple sclerosis
description MicroRNAs (miRNAs) are a recently discovered group of small noncoding RNAs that regulate gene expression post-transcriptionally. They are highly expressed in cells of the immune system, as well as in the central nervous system, and they are deregulated in various neurological disorders. Emerging evidence underlines an involvement of miRNAs in the pathogenesis of Multiple Sclerosis (MS). A number of miRNAs have been found to be dysregulated in blood cells from MS patients, in brain lesions, as well as in biological fluids such as serum and plasma. Despite miRNA altered expression likely showing a high tissue specificity, some profile similarities could be observed for certain miRNAs such as miR-326—such as upregulation in both active lesions and blood—though not for others such as miR-323, which demonstrated upregulation in whole blood, active brain lesions, and T-reg cells, but not in the serum of MS patients. In this review, the possible role of miRNAs in MS pathogenesis will be discussed according to all the available literature, with a particular emphasis on the possibility of considering extracellular miRNAs as a new source for both biomarker identification and therapeutic target discovery.
publisher Molecular Diversity Preservation International (MDPI)
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497323/
_version_ 1611924000879935488