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Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model
Ischemia-reperfusion injury (IRI) following lung transplantation is associated with increased pulmonary inflammatory responses during reperfusion. Mesenchymal stem cells (MSCs) may be able to modulate inflammatory responses in IRI. The aim of the present study was to evaluate the beneficial effects...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665152/ https://www.ncbi.nlm.nih.gov/pubmed/26668605 http://dx.doi.org/10.3892/etm.2015.2806 |
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author | LU, WEIFENG SI, YI DING, JIANYONG CHEN, XIAOLI ZHANG, XIANGMAN DONG, ZHIHUI FU, WEIGUO |
author_facet | LU, WEIFENG SI, YI DING, JIANYONG CHEN, XIAOLI ZHANG, XIANGMAN DONG, ZHIHUI FU, WEIGUO |
author_sort | LU, WEIFENG |
collection | PubMed |
description | Ischemia-reperfusion injury (IRI) following lung transplantation is associated with increased pulmonary inflammatory responses during reperfusion. Mesenchymal stem cells (MSCs) may be able to modulate inflammatory responses in IRI. The aim of the present study was to evaluate the beneficial effects of an intravenous infusion of bone marrow-derived MSCs (BMSCs) in a rat model of pulmonary IRI. IRI was induced in male Lewis rats by 1-h ischemia followed by 2-h reperfusion. The rats received phosphate-buffered saline (PBS) or BMSC infusion at the onset of reperfusion. Pulmonary injury was determined based on the mean blood oxygenation, lung edema and vascular permeability, and performing histopathological examination. Pulmonary inflammation was also evaluated through the examination of the levels of inflammatory cytokines. Compared with the PBS infusion, the BMSC infusion significantly preserved lung function, reduced lung edema and pulmonary microvascular permeability, and decreased the total injury score in rats with IRI. The mRNA levels of the pro-inflammatory cytokines, tumor necrosis factor-α (TNF-α), interleukin (IL)-1β and IL-6, were significantly reduced, while the expression of anti-inflammatory cytokine IL-10 was increased in the rats receiving BMSC infusion. The levels of cytokine-induced neutrophil chemoattractant-1, IL-1β, and TNF-α in bronchoalveolar lavage fluid were also markedly reduced following BMCS infusion. In conclusion, the present results suggested that BMSC infusion exerts protective effects against pulmonary IRI by alleviating IRI-induced inflammation. These findings provide experimental evidence for the treatment of pulmonary IRI using BMSC cell therapy. |
format | Online Article Text |
id | pubmed-4665152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-46651522015-12-14 Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model LU, WEIFENG SI, YI DING, JIANYONG CHEN, XIAOLI ZHANG, XIANGMAN DONG, ZHIHUI FU, WEIGUO Exp Ther Med Articles Ischemia-reperfusion injury (IRI) following lung transplantation is associated with increased pulmonary inflammatory responses during reperfusion. Mesenchymal stem cells (MSCs) may be able to modulate inflammatory responses in IRI. The aim of the present study was to evaluate the beneficial effects of an intravenous infusion of bone marrow-derived MSCs (BMSCs) in a rat model of pulmonary IRI. IRI was induced in male Lewis rats by 1-h ischemia followed by 2-h reperfusion. The rats received phosphate-buffered saline (PBS) or BMSC infusion at the onset of reperfusion. Pulmonary injury was determined based on the mean blood oxygenation, lung edema and vascular permeability, and performing histopathological examination. Pulmonary inflammation was also evaluated through the examination of the levels of inflammatory cytokines. Compared with the PBS infusion, the BMSC infusion significantly preserved lung function, reduced lung edema and pulmonary microvascular permeability, and decreased the total injury score in rats with IRI. The mRNA levels of the pro-inflammatory cytokines, tumor necrosis factor-α (TNF-α), interleukin (IL)-1β and IL-6, were significantly reduced, while the expression of anti-inflammatory cytokine IL-10 was increased in the rats receiving BMSC infusion. The levels of cytokine-induced neutrophil chemoattractant-1, IL-1β, and TNF-α in bronchoalveolar lavage fluid were also markedly reduced following BMCS infusion. In conclusion, the present results suggested that BMSC infusion exerts protective effects against pulmonary IRI by alleviating IRI-induced inflammation. These findings provide experimental evidence for the treatment of pulmonary IRI using BMSC cell therapy. D.A. Spandidos 2015-12 2015-10-15 /pmc/articles/PMC4665152/ /pubmed/26668605 http://dx.doi.org/10.3892/etm.2015.2806 Text en Copyright: © Lu et al. 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 LU, WEIFENG SI, YI DING, JIANYONG CHEN, XIAOLI ZHANG, XIANGMAN DONG, ZHIHUI FU, WEIGUO Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
title | Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
title_full | Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
title_fullStr | Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
title_full_unstemmed | Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
title_short | Mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
title_sort | mesenchymal stem cells attenuate acute ischemia-reperfusion injury in a rat model |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665152/ https://www.ncbi.nlm.nih.gov/pubmed/26668605 http://dx.doi.org/10.3892/etm.2015.2806 |
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