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Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung
PURPOSE: Exposure to radiation provokes cellular responses, which are likely regulated by gene expression networks. MicroRNAs are small non-coding RNAs, which regulate gene expression by promoting mRNA degradation or inhibiting protein translation. The expression patterns of both mRNA and miRNA duri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4044330/ https://www.ncbi.nlm.nih.gov/pubmed/24886372 http://dx.doi.org/10.1186/1748-717X-9-111 |
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author | Xie, Ling Zhou, Jundong Zhang, Shuyu Chen, Qing Lai, Rensheng Ding, Weiqun Song, ChuanJun Meng, XingJun Wu, Jinchang |
author_facet | Xie, Ling Zhou, Jundong Zhang, Shuyu Chen, Qing Lai, Rensheng Ding, Weiqun Song, ChuanJun Meng, XingJun Wu, Jinchang |
author_sort | Xie, Ling |
collection | PubMed |
description | PURPOSE: Exposure to radiation provokes cellular responses, which are likely regulated by gene expression networks. MicroRNAs are small non-coding RNAs, which regulate gene expression by promoting mRNA degradation or inhibiting protein translation. The expression patterns of both mRNA and miRNA during the radiation-induced lung injury (RILI) remain less characterized and the role of miRNAs in the regulation of this process has not been studied. The present study sought to evaluate miRNA and mRNA expression profiles in the rat lung after irradiation. METHODS AND MATERIALS: Male Wistar rats were subjected to single dose irradiation with 20 Gy using 6 MV x-rays to the right lung. (A dose rate of 5 Gy/min was applied). Rats were sacrificed at 3, 12 and 26 weeks after irradiation, and morphological changes in the lung were examined by haematoxylin and eosin. The miRNA and mRNA expression profiles were evaluated by microarrays and followed by quantitative RT-PCR analysis. RESULTS: A cDNA microarray analysis found 2183 transcripts being up-regulated and 2917 transcripts down-regulated (P ≤ 0.05, ≥2.0 fold change) in the lung tissues after irradiation. Likewise, a miRNAs microarray analysis indicated 15 miRNA species being up-regulated and 8 down-regulated (P ≤ 0.05). Subsequent bioinformatics anal -yses of the differentially expressed mRNA and miRNAs revealed that alterations in mRNA expression following irradiation were negatively correlated with miRNAs expression. CONCLUSIONS: Our results provide evidence indicating that irradiation induces alterations of mRNA and miRNA expression in rat lung and that there is a negative correlation of mRNA and miRNA expression levels after irradiation. These findings significantly advance our understanding of the regulatory mechanisms underlying the pathophysiology of radiation-induced lung injury. In summary, RILI does not develop gradually in a linear process. In fact, different cell types interact via cytokines in a very complex network. Furthermore, this study suggests that microRNAs may serve an important role in the pathogenesis of RILI and that understanding their role in RILI may have a significant effect on patient management and diagnosis in the future. |
format | Online Article Text |
id | pubmed-4044330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40443302014-06-05 Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung Xie, Ling Zhou, Jundong Zhang, Shuyu Chen, Qing Lai, Rensheng Ding, Weiqun Song, ChuanJun Meng, XingJun Wu, Jinchang Radiat Oncol Research PURPOSE: Exposure to radiation provokes cellular responses, which are likely regulated by gene expression networks. MicroRNAs are small non-coding RNAs, which regulate gene expression by promoting mRNA degradation or inhibiting protein translation. The expression patterns of both mRNA and miRNA during the radiation-induced lung injury (RILI) remain less characterized and the role of miRNAs in the regulation of this process has not been studied. The present study sought to evaluate miRNA and mRNA expression profiles in the rat lung after irradiation. METHODS AND MATERIALS: Male Wistar rats were subjected to single dose irradiation with 20 Gy using 6 MV x-rays to the right lung. (A dose rate of 5 Gy/min was applied). Rats were sacrificed at 3, 12 and 26 weeks after irradiation, and morphological changes in the lung were examined by haematoxylin and eosin. The miRNA and mRNA expression profiles were evaluated by microarrays and followed by quantitative RT-PCR analysis. RESULTS: A cDNA microarray analysis found 2183 transcripts being up-regulated and 2917 transcripts down-regulated (P ≤ 0.05, ≥2.0 fold change) in the lung tissues after irradiation. Likewise, a miRNAs microarray analysis indicated 15 miRNA species being up-regulated and 8 down-regulated (P ≤ 0.05). Subsequent bioinformatics anal -yses of the differentially expressed mRNA and miRNAs revealed that alterations in mRNA expression following irradiation were negatively correlated with miRNAs expression. CONCLUSIONS: Our results provide evidence indicating that irradiation induces alterations of mRNA and miRNA expression in rat lung and that there is a negative correlation of mRNA and miRNA expression levels after irradiation. These findings significantly advance our understanding of the regulatory mechanisms underlying the pathophysiology of radiation-induced lung injury. In summary, RILI does not develop gradually in a linear process. In fact, different cell types interact via cytokines in a very complex network. Furthermore, this study suggests that microRNAs may serve an important role in the pathogenesis of RILI and that understanding their role in RILI may have a significant effect on patient management and diagnosis in the future. BioMed Central 2014-05-09 /pmc/articles/PMC4044330/ /pubmed/24886372 http://dx.doi.org/10.1186/1748-717X-9-111 Text en Copyright © 2014 Xie et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Xie, Ling Zhou, Jundong Zhang, Shuyu Chen, Qing Lai, Rensheng Ding, Weiqun Song, ChuanJun Meng, XingJun Wu, Jinchang Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung |
title | Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung |
title_full | Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung |
title_fullStr | Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung |
title_full_unstemmed | Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung |
title_short | Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung |
title_sort | integrating microrna and mrna expression profiles in response to radiation-induced injury in rat lung |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4044330/ https://www.ncbi.nlm.nih.gov/pubmed/24886372 http://dx.doi.org/10.1186/1748-717X-9-111 |
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