Cargando…

X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis

Rheumatoid arthritis (RA) is an autoimmune disease that predominantly affects women. MicroRNAs have emerged as crucial regulators of the immune system, whose expression is deregulated in RA. We aimed at quantifying the expression level of 14 miRNAs located on the X chromosome and at identifying whet...

Descripción completa

Detalles Bibliográficos
Autores principales: Khalifa, Olfa, Pers, Yves-Marie, Ferreira, Rosanna, Sénéchal, Audrey, Jorgensen, Christian, Apparailly, Florence, Duroux-Richard, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133852/
https://www.ncbi.nlm.nih.gov/pubmed/27834806
http://dx.doi.org/10.3390/ijms17111852
_version_ 1782471353132122112
author Khalifa, Olfa
Pers, Yves-Marie
Ferreira, Rosanna
Sénéchal, Audrey
Jorgensen, Christian
Apparailly, Florence
Duroux-Richard, Isabelle
author_facet Khalifa, Olfa
Pers, Yves-Marie
Ferreira, Rosanna
Sénéchal, Audrey
Jorgensen, Christian
Apparailly, Florence
Duroux-Richard, Isabelle
author_sort Khalifa, Olfa
collection PubMed
description Rheumatoid arthritis (RA) is an autoimmune disease that predominantly affects women. MicroRNAs have emerged as crucial regulators of the immune system, whose expression is deregulated in RA. We aimed at quantifying the expression level of 14 miRNAs located on the X chromosome and at identifying whether differences are associated with disease and/or sex. A case–control study of 21 RA patients and 22 age- and sex-matched healthy controls was performed on peripheral blood mononuclear cells. The expression level of five miRNAs (miR-221, miR-222, miR-532, miR-106a, and miR-98) was significantly different between RA and controls when stratifying by sex, and the expression level of four miRNAs (miR-222, miR-532, miR-98, and miR-92a) was significantly different between RA females and males. The expression quantitative trait loci (eQTL) analysis revealed a significant gender effect of the FoxP3 promoter polymorphism rs3761548A/C on miR-221, miR-222 and miR-532 expression levels, and of the FoxP3 polymorphism rs2232365A/G on miR-221 expression levels in PBMC of RA patients. These data further support the involvement of the X chromosome in RA susceptibility. X-linked miRNAs, in the context of sex differences, might provide novel insight into new molecular mechanisms and potential therapeutic targets in RA for disease treatment and prevention.
format Online
Article
Text
id pubmed-5133852
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-51338522016-12-12 X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis Khalifa, Olfa Pers, Yves-Marie Ferreira, Rosanna Sénéchal, Audrey Jorgensen, Christian Apparailly, Florence Duroux-Richard, Isabelle Int J Mol Sci Article Rheumatoid arthritis (RA) is an autoimmune disease that predominantly affects women. MicroRNAs have emerged as crucial regulators of the immune system, whose expression is deregulated in RA. We aimed at quantifying the expression level of 14 miRNAs located on the X chromosome and at identifying whether differences are associated with disease and/or sex. A case–control study of 21 RA patients and 22 age- and sex-matched healthy controls was performed on peripheral blood mononuclear cells. The expression level of five miRNAs (miR-221, miR-222, miR-532, miR-106a, and miR-98) was significantly different between RA and controls when stratifying by sex, and the expression level of four miRNAs (miR-222, miR-532, miR-98, and miR-92a) was significantly different between RA females and males. The expression quantitative trait loci (eQTL) analysis revealed a significant gender effect of the FoxP3 promoter polymorphism rs3761548A/C on miR-221, miR-222 and miR-532 expression levels, and of the FoxP3 polymorphism rs2232365A/G on miR-221 expression levels in PBMC of RA patients. These data further support the involvement of the X chromosome in RA susceptibility. X-linked miRNAs, in the context of sex differences, might provide novel insight into new molecular mechanisms and potential therapeutic targets in RA for disease treatment and prevention. MDPI 2016-11-08 /pmc/articles/PMC5133852/ /pubmed/27834806 http://dx.doi.org/10.3390/ijms17111852 Text en © 2016 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
Khalifa, Olfa
Pers, Yves-Marie
Ferreira, Rosanna
Sénéchal, Audrey
Jorgensen, Christian
Apparailly, Florence
Duroux-Richard, Isabelle
X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis
title X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis
title_full X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis
title_fullStr X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis
title_full_unstemmed X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis
title_short X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis
title_sort x-linked mirnas associated with gender differences in rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133852/
https://www.ncbi.nlm.nih.gov/pubmed/27834806
http://dx.doi.org/10.3390/ijms17111852
work_keys_str_mv AT khalifaolfa xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis
AT persyvesmarie xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis
AT ferreirarosanna xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis
AT senechalaudrey xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis
AT jorgensenchristian xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis
AT apparaillyflorence xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis
AT durouxrichardisabelle xlinkedmirnasassociatedwithgenderdifferencesinrheumatoidarthritis