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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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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 |
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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 |
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