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Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March
(1) Background: The atopic march is defined by the increased prevalence of allergic diseases after atopic dermatitis onset. In fact, atopic dermatitis is believed to play an important role in allergen sensitization via the damaged skin barrier, leading to allergic diseases such as allergic asthma an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730597/ https://www.ncbi.nlm.nih.gov/pubmed/33260893 http://dx.doi.org/10.3390/ijms21239011 |
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author | Bélanger, Émile Madore, Anne-Marie Boucher-Lafleur, Anne-Marie Simon, Marie-Michelle Kwan, Tony Pastinen, Tomi Laprise, Catherine |
author_facet | Bélanger, Émile Madore, Anne-Marie Boucher-Lafleur, Anne-Marie Simon, Marie-Michelle Kwan, Tony Pastinen, Tomi Laprise, Catherine |
author_sort | Bélanger, Émile |
collection | PubMed |
description | (1) Background: The atopic march is defined by the increased prevalence of allergic diseases after atopic dermatitis onset. In fact, atopic dermatitis is believed to play an important role in allergen sensitization via the damaged skin barrier, leading to allergic diseases such as allergic asthma and allergic rhinitis. The eosinophil, a pro-inflammatory cell that contributes to epithelial damage, is one of the various cells recruited in the inflammatory reactions characterizing these diseases. Few studies were conducted on the transcriptome of this cell type and even less on their specific microRNA (miRNA) profile, which could modulate pathogenesis of allergic diseases and clinical manifestations post-transcriptionally. Actually, their implication in allergic diseases is not fully understood, but they are believed to play a role in inflammation-related patterns and epithelial cell proliferation. (2) Methods: Next-generation sequencing was performed on RNA samples from eosinophils of individuals with atopic dermatitis, atopy, allergic rhinitis and asthma to obtain differential counts of primary miRNA (pri-miRNA); these were also analyzed for asthma-related phenotypes such as forced expiratory volume in one second (FEV(1)), immunoglobulin E (IgE) and provocative concentration of methacholine inducing a 20% fall in forced expiratory volume in 1 s (PC(20)) levels, as well as FEV(1) to forced vital capacity (FEV(1)/FVC) ratio. (3) Results: Eighteen miRNAs from eosinophils were identified to be significantly different between affected individuals and unaffected ones. Based on counts from these miRNAs, individuals were then clustered into groups using Ward’s method on Euclidian distances. Groups were found to be explained by asthma diagnosis, familial history of respiratory diseases and allergic rhinitis as well as neutrophil counts. (4) Conclusions: The 18 differential miRNA counts for the studying phenotypes allow a better understanding of the epigenetic mechanisms underlying the development of the allergic diseases included in the atopic march. |
format | Online Article Text |
id | pubmed-7730597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77305972020-12-12 Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March Bélanger, Émile Madore, Anne-Marie Boucher-Lafleur, Anne-Marie Simon, Marie-Michelle Kwan, Tony Pastinen, Tomi Laprise, Catherine Int J Mol Sci Article (1) Background: The atopic march is defined by the increased prevalence of allergic diseases after atopic dermatitis onset. In fact, atopic dermatitis is believed to play an important role in allergen sensitization via the damaged skin barrier, leading to allergic diseases such as allergic asthma and allergic rhinitis. The eosinophil, a pro-inflammatory cell that contributes to epithelial damage, is one of the various cells recruited in the inflammatory reactions characterizing these diseases. Few studies were conducted on the transcriptome of this cell type and even less on their specific microRNA (miRNA) profile, which could modulate pathogenesis of allergic diseases and clinical manifestations post-transcriptionally. Actually, their implication in allergic diseases is not fully understood, but they are believed to play a role in inflammation-related patterns and epithelial cell proliferation. (2) Methods: Next-generation sequencing was performed on RNA samples from eosinophils of individuals with atopic dermatitis, atopy, allergic rhinitis and asthma to obtain differential counts of primary miRNA (pri-miRNA); these were also analyzed for asthma-related phenotypes such as forced expiratory volume in one second (FEV(1)), immunoglobulin E (IgE) and provocative concentration of methacholine inducing a 20% fall in forced expiratory volume in 1 s (PC(20)) levels, as well as FEV(1) to forced vital capacity (FEV(1)/FVC) ratio. (3) Results: Eighteen miRNAs from eosinophils were identified to be significantly different between affected individuals and unaffected ones. Based on counts from these miRNAs, individuals were then clustered into groups using Ward’s method on Euclidian distances. Groups were found to be explained by asthma diagnosis, familial history of respiratory diseases and allergic rhinitis as well as neutrophil counts. (4) Conclusions: The 18 differential miRNA counts for the studying phenotypes allow a better understanding of the epigenetic mechanisms underlying the development of the allergic diseases included in the atopic march. MDPI 2020-11-27 /pmc/articles/PMC7730597/ /pubmed/33260893 http://dx.doi.org/10.3390/ijms21239011 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 Bélanger, Émile Madore, Anne-Marie Boucher-Lafleur, Anne-Marie Simon, Marie-Michelle Kwan, Tony Pastinen, Tomi Laprise, Catherine Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March |
title | Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March |
title_full | Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March |
title_fullStr | Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March |
title_full_unstemmed | Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March |
title_short | Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March |
title_sort | eosinophil micrornas play a regulatory role in allergic diseases included in the atopic march |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730597/ https://www.ncbi.nlm.nih.gov/pubmed/33260893 http://dx.doi.org/10.3390/ijms21239011 |
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