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Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis

This study tested the hypothesis that xenogeneic human umbilical cord-derived mesenchymal stem cell (HUCDMSC) therapy would improve survival rates in rats with acute respiratory distress-syndrome (ARDS, induction by 48 h inhalation of 100% oxygen) and sepsis-syndrome (SS, induction by cecal-ligation...

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Autores principales: Lee, Fan-Yen, Chen, Kuan-Hung, Wallace, Christopher Glenn, Sung, Pei-Hsun, Sheu, Jiunn-Jye, Chung, Sheng-Ying, Chen, Yung-Lung, Lu, Hung-I, Ko, Sheung-Fat, Sun, Cheuk-Kwan, Chiang, Hsin-Ju, Chang, Hsueh-Wen, Lee, Mel S., Yip, Hon-Kan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542214/
https://www.ncbi.nlm.nih.gov/pubmed/28484089
http://dx.doi.org/10.18632/oncotarget.17320
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author Lee, Fan-Yen
Chen, Kuan-Hung
Wallace, Christopher Glenn
Sung, Pei-Hsun
Sheu, Jiunn-Jye
Chung, Sheng-Ying
Chen, Yung-Lung
Lu, Hung-I
Ko, Sheung-Fat
Sun, Cheuk-Kwan
Chiang, Hsin-Ju
Chang, Hsueh-Wen
Lee, Mel S.
Yip, Hon-Kan
author_facet Lee, Fan-Yen
Chen, Kuan-Hung
Wallace, Christopher Glenn
Sung, Pei-Hsun
Sheu, Jiunn-Jye
Chung, Sheng-Ying
Chen, Yung-Lung
Lu, Hung-I
Ko, Sheung-Fat
Sun, Cheuk-Kwan
Chiang, Hsin-Ju
Chang, Hsueh-Wen
Lee, Mel S.
Yip, Hon-Kan
author_sort Lee, Fan-Yen
collection PubMed
description This study tested the hypothesis that xenogeneic human umbilical cord-derived mesenchymal stem cell (HUCDMSC) therapy would improve survival rates in rats with acute respiratory distress-syndrome (ARDS, induction by 48 h inhalation of 100% oxygen) and sepsis-syndrome (SS, induction by cecal-ligation and puncture) (ARDS-SS). Adult-male Sprague-Dawley rats were categorized into group 1 (sham-controls), group 2 (ARDS-SS), group 3 [ARDS-SS+HUCDMSC (1.2 ×10(6) cells administered 1 h after SS-induction)], and group 4 [ARDS-SS+HUCDMSC (1.2 ×10(6) cells administered 24 h after SS-induction)]. The mortality rate was higher in groups 2 and 4 than in groups 1 and 3 (all p<0.0001). The blood pressure after 28 h was lower in groups 2, 3 and 4 (p<0.0001) than in group 1. Albumin levels and percentages of inflammatory cells in broncho-alveolar lavage fluid, and the percentages of inflammatory and immune cells in circulation, were lowest in group 1, highest in group 2, and higher in group 3 than group 4 (all p<0.0001). The percentages of inflammatory cells in ascites and kidney parenchyma showed identical patterns, as did kidney injury scores (all p<0.0001). EarlyHUCDMSC therapy reduced rodent mortality after induced ARDS-SS.
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spelling pubmed-55422142017-08-07 Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis Lee, Fan-Yen Chen, Kuan-Hung Wallace, Christopher Glenn Sung, Pei-Hsun Sheu, Jiunn-Jye Chung, Sheng-Ying Chen, Yung-Lung Lu, Hung-I Ko, Sheung-Fat Sun, Cheuk-Kwan Chiang, Hsin-Ju Chang, Hsueh-Wen Lee, Mel S. Yip, Hon-Kan Oncotarget Research Paper This study tested the hypothesis that xenogeneic human umbilical cord-derived mesenchymal stem cell (HUCDMSC) therapy would improve survival rates in rats with acute respiratory distress-syndrome (ARDS, induction by 48 h inhalation of 100% oxygen) and sepsis-syndrome (SS, induction by cecal-ligation and puncture) (ARDS-SS). Adult-male Sprague-Dawley rats were categorized into group 1 (sham-controls), group 2 (ARDS-SS), group 3 [ARDS-SS+HUCDMSC (1.2 ×10(6) cells administered 1 h after SS-induction)], and group 4 [ARDS-SS+HUCDMSC (1.2 ×10(6) cells administered 24 h after SS-induction)]. The mortality rate was higher in groups 2 and 4 than in groups 1 and 3 (all p<0.0001). The blood pressure after 28 h was lower in groups 2, 3 and 4 (p<0.0001) than in group 1. Albumin levels and percentages of inflammatory cells in broncho-alveolar lavage fluid, and the percentages of inflammatory and immune cells in circulation, were lowest in group 1, highest in group 2, and higher in group 3 than group 4 (all p<0.0001). The percentages of inflammatory cells in ascites and kidney parenchyma showed identical patterns, as did kidney injury scores (all p<0.0001). EarlyHUCDMSC therapy reduced rodent mortality after induced ARDS-SS. Impact Journals LLC 2017-04-21 /pmc/articles/PMC5542214/ /pubmed/28484089 http://dx.doi.org/10.18632/oncotarget.17320 Text en Copyright: © 2017 Lee et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Lee, Fan-Yen
Chen, Kuan-Hung
Wallace, Christopher Glenn
Sung, Pei-Hsun
Sheu, Jiunn-Jye
Chung, Sheng-Ying
Chen, Yung-Lung
Lu, Hung-I
Ko, Sheung-Fat
Sun, Cheuk-Kwan
Chiang, Hsin-Ju
Chang, Hsueh-Wen
Lee, Mel S.
Yip, Hon-Kan
Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
title Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
title_full Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
title_fullStr Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
title_full_unstemmed Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
title_short Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
title_sort xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542214/
https://www.ncbi.nlm.nih.gov/pubmed/28484089
http://dx.doi.org/10.18632/oncotarget.17320
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