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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...

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Autores principales: Chang, Wei-An, Tsai, Ming-Ju, Jian, Shu-Fang, Sheu, Chau-Chyun, Kuo, Po-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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.
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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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