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Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics
INTRODUCTION: COPD is a chronic inflammatory disease of lung. The inflammatory response in COPD is associated with neutrophils, macrophages, T lymphocytes, and bronchial epithelial cells, and occurs mainly in the small airway, leading to irreversible airflow limitation. METHODS: In order to investig...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089098/ https://www.ncbi.nlm.nih.gov/pubmed/30127601 http://dx.doi.org/10.2147/COPD.S173206 |
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author | Chang, Wei-An Tsai, Ming-Ju Jian, Shu-Fang Sheu, Chau-Chyun Kuo, Po-Lin |
author_facet | Chang, Wei-An Tsai, Ming-Ju Jian, Shu-Fang Sheu, Chau-Chyun Kuo, Po-Lin |
author_sort | Chang, Wei-An |
collection | PubMed |
description | INTRODUCTION: COPD is a chronic inflammatory disease of lung. The inflammatory response in COPD is associated with neutrophils, macrophages, T lymphocytes, and bronchial epithelial cells, and occurs mainly in the small airway, leading to irreversible airflow limitation. METHODS: In order to investigate the microRNA–mRNA interaction in the microenvironment of the COPD airway, we used next-generation sequencing and bioinformatics in this study. RESULTS: We identified four genes with microRNA–mRNA interactions involved in COPD small-airway bronchial epithelial cells: NT5E, SDK1, TNS1, and PCDH7. Furthermore, miR6511a-5p–NT5E interaction was found to be involved in small-airway bronchial epithelial cells, large-airway bronchial epithelial cells, and alveolar macrophages. CONCLUSION: Our results showed that miR6511a-5p–NT5E interaction plays an important role in COPD, which might be associated with cell–cell contact, activation of leukocytes, activation of T lymphocytes, and cellular homeostasis. These findings provide new information for further investigations of the COPD microenvironment, and may help to develop new diagnostic or therapeutic strategies targeting the bronchial epithelium for COPD. |
format | Online Article Text |
id | pubmed-6089098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60890982018-08-20 Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics Chang, Wei-An Tsai, Ming-Ju Jian, Shu-Fang Sheu, Chau-Chyun Kuo, Po-Lin Int J Chron Obstruct Pulmon Dis Original Research INTRODUCTION: COPD is a chronic inflammatory disease of lung. The inflammatory response in COPD is associated with neutrophils, macrophages, T lymphocytes, and bronchial epithelial cells, and occurs mainly in the small airway, leading to irreversible airflow limitation. METHODS: In order to investigate the microRNA–mRNA interaction in the microenvironment of the COPD airway, we used next-generation sequencing and bioinformatics in this study. RESULTS: We identified four genes with microRNA–mRNA interactions involved in COPD small-airway bronchial epithelial cells: NT5E, SDK1, TNS1, and PCDH7. Furthermore, miR6511a-5p–NT5E interaction was found to be involved in small-airway bronchial epithelial cells, large-airway bronchial epithelial cells, and alveolar macrophages. CONCLUSION: Our results showed that miR6511a-5p–NT5E interaction plays an important role in COPD, which might be associated with cell–cell contact, activation of leukocytes, activation of T lymphocytes, and cellular homeostasis. These findings provide new information for further investigations of the COPD microenvironment, and may help to develop new diagnostic or therapeutic strategies targeting the bronchial epithelium for COPD. Dove Medical Press 2018-08-10 /pmc/articles/PMC6089098/ /pubmed/30127601 http://dx.doi.org/10.2147/COPD.S173206 Text en © 2018 Chang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chang, Wei-An Tsai, Ming-Ju Jian, Shu-Fang Sheu, Chau-Chyun Kuo, Po-Lin Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics |
title | Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics |
title_full | Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics |
title_fullStr | Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics |
title_full_unstemmed | Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics |
title_short | Systematic analysis of transcriptomic profiles of COPD airway epithelium using next-generation sequencing and bioinformatics |
title_sort | systematic analysis of transcriptomic profiles of copd airway epithelium using next-generation sequencing and bioinformatics |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089098/ https://www.ncbi.nlm.nih.gov/pubmed/30127601 http://dx.doi.org/10.2147/COPD.S173206 |
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