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

  • Fan Yen Lee
  • , Kuan Hung Chen
  • , Christopher Glenn Wallace
  • , Pei Hsun Sung
  • , Jiunn Jye Sheu
  • , Sheng Ying Chung
  • , Yung Lung Chen
  • , Hung I. Lu
  • , Sheung Fat Ko
  • , Cheuk Kwan Sun
  • , Hsin Ju Chiang
  • , Hsueh Wen Chang
  • , Mel S. Lee
  • , Hon Kan Yip*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

43 Scopus citations

Abstract

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) (ARDSSS). Adult-male Sprague-Dawley rats were categorized into group 1 (sham-controls), group 2 (ARDS-SS), group 3 [ARDS-SS+HUCDMSC (1.2 x106 cells administered 1 h after SS-induction)], and group 4 [ARDS-SS+HUCDMSC (1.2 x106 cells administered24 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.

Original languageEnglish
Pages (from-to)45626-45642
Number of pages17
JournalOncotarget
Volume8
Issue number28
DOIs
StatePublished - 2017

Bibliographical note

Publisher Copyright:
© Lee et al.

Keywords

  • Inflammatory and immune reactions
  • Keywords: acute respiratory distress syndrome
  • Mortality
  • Sepsis syndrome
  • Xenogeneic mesenchymal stem cell

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