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Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts

COPD is associated with disturbed tissue repair, possibly due to TGF-β-regulated miRNA changes in fibroblasts. Our aim was to identify TGF-β-regulated miRNAs and their differential regulation and expression in COPD compared to control fibroblasts. Small RNA sequencing was performed on TGF-β-stimulat...

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Autores principales: Ong, J., Faiz, A., Timens, W., van den Berge, M., Terpstra, M. M., Kok, K., van den Berg, A., Kluiver, J., Brandsma, C. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890791/
https://www.ncbi.nlm.nih.gov/pubmed/31796837
http://dx.doi.org/10.1038/s41598-019-54728-4
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author Ong, J.
Faiz, A.
Timens, W.
van den Berge, M.
Terpstra, M. M.
Kok, K.
van den Berg, A.
Kluiver, J.
Brandsma, C. A.
author_facet Ong, J.
Faiz, A.
Timens, W.
van den Berge, M.
Terpstra, M. M.
Kok, K.
van den Berg, A.
Kluiver, J.
Brandsma, C. A.
author_sort Ong, J.
collection PubMed
description COPD is associated with disturbed tissue repair, possibly due to TGF-β-regulated miRNA changes in fibroblasts. Our aim was to identify TGF-β-regulated miRNAs and their differential regulation and expression in COPD compared to control fibroblasts. Small RNA sequencing was performed on TGF-β-stimulated and unstimulated lung fibroblasts from 15 COPD patients and 15 controls. Linear regression was used to identify TGF-β-regulated and COPD-associated miRNAs. Interaction analysis was performed to compare miRNAs that responded differently to TGF-β in COPD and control. Re-analysis of previously generated Ago2-IP data and Enrichr were used to identify presence and function of potential target genes in the miRNA-targetome of lung fibroblasts. In total, 46 TGF-β-regulated miRNAs were identified in COPD and 86 in control fibroblasts (FDR < 0.05). MiR-27a-5p was the most significantly upregulated miRNA. MiR-148b-3p, miR-589-5p and miR-376b-3p responded differently to TGF-β in COPD compared to control (FDR < 0.25). MiR-660-5p was significantly upregulated in COPD compared to control (FDR < 0.05). Several predicted targets of miR-27a-5p, miR-148b-3p and miR-660-5p were present in the miRNA-targetome, and were mainly involved in the regulation of gene transcription. In conclusion, altered TGF-β-induced miRNA regulation and differential expression of miR-660-5p in COPD fibroblasts, may represent one of the mechanisms underlying aberrant tissue repair and remodelling in COPD.
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spelling pubmed-68907912019-12-10 Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts Ong, J. Faiz, A. Timens, W. van den Berge, M. Terpstra, M. M. Kok, K. van den Berg, A. Kluiver, J. Brandsma, C. A. Sci Rep Article COPD is associated with disturbed tissue repair, possibly due to TGF-β-regulated miRNA changes in fibroblasts. Our aim was to identify TGF-β-regulated miRNAs and their differential regulation and expression in COPD compared to control fibroblasts. Small RNA sequencing was performed on TGF-β-stimulated and unstimulated lung fibroblasts from 15 COPD patients and 15 controls. Linear regression was used to identify TGF-β-regulated and COPD-associated miRNAs. Interaction analysis was performed to compare miRNAs that responded differently to TGF-β in COPD and control. Re-analysis of previously generated Ago2-IP data and Enrichr were used to identify presence and function of potential target genes in the miRNA-targetome of lung fibroblasts. In total, 46 TGF-β-regulated miRNAs were identified in COPD and 86 in control fibroblasts (FDR < 0.05). MiR-27a-5p was the most significantly upregulated miRNA. MiR-148b-3p, miR-589-5p and miR-376b-3p responded differently to TGF-β in COPD compared to control (FDR < 0.25). MiR-660-5p was significantly upregulated in COPD compared to control (FDR < 0.05). Several predicted targets of miR-27a-5p, miR-148b-3p and miR-660-5p were present in the miRNA-targetome, and were mainly involved in the regulation of gene transcription. In conclusion, altered TGF-β-induced miRNA regulation and differential expression of miR-660-5p in COPD fibroblasts, may represent one of the mechanisms underlying aberrant tissue repair and remodelling in COPD. Nature Publishing Group UK 2019-12-03 /pmc/articles/PMC6890791/ /pubmed/31796837 http://dx.doi.org/10.1038/s41598-019-54728-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ong, J.
Faiz, A.
Timens, W.
van den Berge, M.
Terpstra, M. M.
Kok, K.
van den Berg, A.
Kluiver, J.
Brandsma, C. A.
Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts
title Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts
title_full Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts
title_fullStr Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts
title_full_unstemmed Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts
title_short Marked TGF-β-regulated miRNA expression changes in both COPD and control lung fibroblasts
title_sort marked tgf-β-regulated mirna expression changes in both copd and control lung fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890791/
https://www.ncbi.nlm.nih.gov/pubmed/31796837
http://dx.doi.org/10.1038/s41598-019-54728-4
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