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Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences

Current studies evidence the role of miRNAs in extracellular vesicles (EVs) as key regulators of pathological processes, including neuroinflammation and neurodegeneration. As EVs can cross the blood–brain barrier, and EV miRNAs are very stable in peripheral circulation, we evaluated the potential ge...

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Autores principales: Ibáñez, Francesc, Ureña-Peralta, Juan R., Costa-Alba, Pilar, Torres, Jorge-Luis, Laso, Francisco-Javier, Marcos, Miguel, Guerri, Consuelo, Pascual, María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555060/
https://www.ncbi.nlm.nih.gov/pubmed/32937997
http://dx.doi.org/10.3390/ijms21186730
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author Ibáñez, Francesc
Ureña-Peralta, Juan R.
Costa-Alba, Pilar
Torres, Jorge-Luis
Laso, Francisco-Javier
Marcos, Miguel
Guerri, Consuelo
Pascual, María
author_facet Ibáñez, Francesc
Ureña-Peralta, Juan R.
Costa-Alba, Pilar
Torres, Jorge-Luis
Laso, Francisco-Javier
Marcos, Miguel
Guerri, Consuelo
Pascual, María
author_sort Ibáñez, Francesc
collection PubMed
description Current studies evidence the role of miRNAs in extracellular vesicles (EVs) as key regulators of pathological processes, including neuroinflammation and neurodegeneration. As EVs can cross the blood–brain barrier, and EV miRNAs are very stable in peripheral circulation, we evaluated the potential gender differences in inflammatory-regulated miRNAs levels in human and murine plasma EVs derived from alcohol-intoxicated female and male adolescents, and whether these miRNAs could be used as biomarkers of neuroinflammation. We demonstrated that while alcohol intoxication lowers anti-inflammatory miRNA (mir-146a-5p, mir-21-5p, mir-182-5p) levels in plasma EVs from human and mice female adolescents, these EV miRNAs increased in males. In mice brain cortices, ethanol treatment lowers mir-146a-5p and mir-21-5p levels, while triggering a higher expression of inflammatory target genes (Traf6, Stat3, and Camk2a) in adolescent female mice. These results indicate, for the first time, that female and male adolescents differ as regards the ethanol effects associated with the inflammatory-related plasma miRNAs EVs profile, and suggest that female adolescents are more vulnerable than males to the inflammatory effects of binge alcohol drinking. These findings also support the view that circulating miRNAs in EVs could be useful biomarkers for screening ethanol-induced neuroinflammation and brain damage in adolescence.
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spelling pubmed-75550602020-10-14 Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences Ibáñez, Francesc Ureña-Peralta, Juan R. Costa-Alba, Pilar Torres, Jorge-Luis Laso, Francisco-Javier Marcos, Miguel Guerri, Consuelo Pascual, María Int J Mol Sci Article Current studies evidence the role of miRNAs in extracellular vesicles (EVs) as key regulators of pathological processes, including neuroinflammation and neurodegeneration. As EVs can cross the blood–brain barrier, and EV miRNAs are very stable in peripheral circulation, we evaluated the potential gender differences in inflammatory-regulated miRNAs levels in human and murine plasma EVs derived from alcohol-intoxicated female and male adolescents, and whether these miRNAs could be used as biomarkers of neuroinflammation. We demonstrated that while alcohol intoxication lowers anti-inflammatory miRNA (mir-146a-5p, mir-21-5p, mir-182-5p) levels in plasma EVs from human and mice female adolescents, these EV miRNAs increased in males. In mice brain cortices, ethanol treatment lowers mir-146a-5p and mir-21-5p levels, while triggering a higher expression of inflammatory target genes (Traf6, Stat3, and Camk2a) in adolescent female mice. These results indicate, for the first time, that female and male adolescents differ as regards the ethanol effects associated with the inflammatory-related plasma miRNAs EVs profile, and suggest that female adolescents are more vulnerable than males to the inflammatory effects of binge alcohol drinking. These findings also support the view that circulating miRNAs in EVs could be useful biomarkers for screening ethanol-induced neuroinflammation and brain damage in adolescence. MDPI 2020-09-14 /pmc/articles/PMC7555060/ /pubmed/32937997 http://dx.doi.org/10.3390/ijms21186730 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ibáñez, Francesc
Ureña-Peralta, Juan R.
Costa-Alba, Pilar
Torres, Jorge-Luis
Laso, Francisco-Javier
Marcos, Miguel
Guerri, Consuelo
Pascual, María
Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences
title Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences
title_full Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences
title_fullStr Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences
title_full_unstemmed Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences
title_short Circulating MicroRNAs in Extracellular Vesicles as Potential Biomarkers of Alcohol-Induced Neuroinflammation in Adolescence: Gender Differences
title_sort circulating micrornas in extracellular vesicles as potential biomarkers of alcohol-induced neuroinflammation in adolescence: gender differences
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555060/
https://www.ncbi.nlm.nih.gov/pubmed/32937997
http://dx.doi.org/10.3390/ijms21186730
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