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MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice

Previous studies have shown that microRNAs (miRs), such as miR-146a play an important role in the pathogenesis of intestinal ischemia/reperfusion (I/R)-induced injury; however, the role of miR-146a in intestinal I/R-induced acute lung injury has not been elucidated. An intestinal I/R-induced injury...

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Autores principales: Li, Gehui, Xu, Min, Wang, Hao, Qi, Xiaofei, Wang, Xiaoguang, Li, Yong, Sun, Jing, Li, Yuantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290461/
https://www.ncbi.nlm.nih.gov/pubmed/34335886
http://dx.doi.org/10.3892/etm.2021.10369
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author Li, Gehui
Xu, Min
Wang, Hao
Qi, Xiaofei
Wang, Xiaoguang
Li, Yong
Sun, Jing
Li, Yuantao
author_facet Li, Gehui
Xu, Min
Wang, Hao
Qi, Xiaofei
Wang, Xiaoguang
Li, Yong
Sun, Jing
Li, Yuantao
author_sort Li, Gehui
collection PubMed
description Previous studies have shown that microRNAs (miRs), such as miR-146a play an important role in the pathogenesis of intestinal ischemia/reperfusion (I/R)-induced injury; however, the role of miR-146a in intestinal I/R-induced acute lung injury has not been elucidated. An intestinal I/R-induced injury mouse model was established in the present study by clamping the superior mesenteric artery and expression levels of miR-146a in intestinal and lung tissue samples were evaluated using reverse transcription-quantitative PCR (RT-qPCR). Intestinal and lung histopathological characteristics in mice with intestinal I/R-induced injury were assessed by hematoxylin and eosin staining, and mRNA and protein expression levels in intestinal and lung tissue samples were evaluated using RT-qPCR and western blotting, respectively. miR-146a expression was significantly downregulated in the intestinal and lung tissue samples of mice with intestinal I/R-induced injury. Intestinal I/R injury-induced histopathological changes in the lung and intestines, and pulmonary edema in mice transduced with an adenoviral miR-146a-overexpression vector (the miR-146a overexpression group) were alleviated. mRNA expression levels of TNF-α, IL-1β, IFN-γ and TGF-β1, and protein expression levels of TNF receptor-associated factor 6, phosphorylated-p65 NF-κB, cleaved caspase-3 and cleaved caspase-9 in lung and intestinal tissue samples were downregulated in I/R-miR-146a-overexpressing mice, compared with those from the I/R-negative control group. Thus, the present study identified that pre-treatment with the miR-146a overexpression vector alleviated intestinal I/R-induced acute lung injury in mice.
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spelling pubmed-82904612021-07-30 MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice Li, Gehui Xu, Min Wang, Hao Qi, Xiaofei Wang, Xiaoguang Li, Yong Sun, Jing Li, Yuantao Exp Ther Med Articles Previous studies have shown that microRNAs (miRs), such as miR-146a play an important role in the pathogenesis of intestinal ischemia/reperfusion (I/R)-induced injury; however, the role of miR-146a in intestinal I/R-induced acute lung injury has not been elucidated. An intestinal I/R-induced injury mouse model was established in the present study by clamping the superior mesenteric artery and expression levels of miR-146a in intestinal and lung tissue samples were evaluated using reverse transcription-quantitative PCR (RT-qPCR). Intestinal and lung histopathological characteristics in mice with intestinal I/R-induced injury were assessed by hematoxylin and eosin staining, and mRNA and protein expression levels in intestinal and lung tissue samples were evaluated using RT-qPCR and western blotting, respectively. miR-146a expression was significantly downregulated in the intestinal and lung tissue samples of mice with intestinal I/R-induced injury. Intestinal I/R injury-induced histopathological changes in the lung and intestines, and pulmonary edema in mice transduced with an adenoviral miR-146a-overexpression vector (the miR-146a overexpression group) were alleviated. mRNA expression levels of TNF-α, IL-1β, IFN-γ and TGF-β1, and protein expression levels of TNF receptor-associated factor 6, phosphorylated-p65 NF-κB, cleaved caspase-3 and cleaved caspase-9 in lung and intestinal tissue samples were downregulated in I/R-miR-146a-overexpressing mice, compared with those from the I/R-negative control group. Thus, the present study identified that pre-treatment with the miR-146a overexpression vector alleviated intestinal I/R-induced acute lung injury in mice. D.A. Spandidos 2021-09 2021-07-01 /pmc/articles/PMC8290461/ /pubmed/34335886 http://dx.doi.org/10.3892/etm.2021.10369 Text en Copyright: © Li et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Li, Gehui
Xu, Min
Wang, Hao
Qi, Xiaofei
Wang, Xiaoguang
Li, Yong
Sun, Jing
Li, Yuantao
MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
title MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
title_full MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
title_fullStr MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
title_full_unstemmed MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
title_short MicroRNA-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
title_sort microrna-146a overexpression alleviates intestinal ischemia/reperfusion-induced acute lung injury in mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290461/
https://www.ncbi.nlm.nih.gov/pubmed/34335886
http://dx.doi.org/10.3892/etm.2021.10369
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