Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (27): 5011-5016.doi: 10.3969/j.issn.2095-4344.2012.27.014

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Hyperbaric oxygenation for theraputic angiogenesis acquired by transplantation of vascular endothelial growth factor gene modified bone marrow mesenchymal stem cells in rats with myocardial infarction

Gao Feng1, Zhang Jin-bao1, Zhou Kai1, Ouyang Hui1, Tang Ke1, Wu Xiao-chen1, He Chun-yang2, Liu Wei-yong3   

  1. 1Department of Cardiothoracic Surgery,
    2Department of Hyperbaric Oxygenation, Chengdu Military General Hospital, Chendu 610083, Sichuan Province, China;
    3Institute of Cardiovascular Surgery, Xijing Hospital, Fourth Military Medical University of Chinese PLA, Xi’an 710033, Shaanxi Province, China
  • Received:2012-04-06 Revised:2012-06-04 Online:2012-07-01 Published:2013-11-01
  • Contact: Zhang Jin-bao, Professor, Department of Cardiothoracic Surgery, Chengdu Military General Hospital, Chendu 610083, Sichuan Province, China wanderer_001@163.com
  • About author:Gao Feng☆, M.D., Attending physician, Department of Cardiothoracic Surgery, Chengdu Military General Hospital, Chendu 610083, Sichuan Province, China cardiomountain@163.com

Abstract:

BACKGROUND: The pathological changes of bone marrow mesenchymal stem cells after transplantation into peri-infarct myocardium including ischemia, hypoxia, inflammation, and cell apoptosis greatly influence the survival of transplanted bone marrow mesenchymal stem cells, while hyperbaric oxygenation can significantly improve the hypoxic state.
OBJECTIVE: To investigate the effects of hyperbaric oxygenation for therapeutic angiogenesis acquired by transplantation of vascular endothelial growth factor gene modified bone marrow mesenchymal stemcells in rats with myocardial infarction.
METHODS: Rat bone marrow mesenchymal stem cells transfected with eukaryotic expression vector pcDNA3.1(-)/VEGF165 were transplanted into the ischemic tissue of a rat model of myocardial infarction. Prior to transplantation, rat bone marrow mesenchymal stem cells were labeled with CM-Dil. Within 2 weeks after transplantation, hyperbaric oxygenation was performed daily. At 1 month after transplantation, the left ventricular ejection fraction was measured by ultrasonic cardiogram, the density of newly formed vessels was determined by histochemical, hematoxylin-eosin, and Ⅷ factor staining.
RESULTS AND CONCLUSION: CM-DiI could label nearly 100% bone marrow mesenchymal stem cells. At 1 month after transplantation, the left ventricular ejection fraction and the density of newly formed vessels in rats subjected to hyperbaric oxygenation were significantly increased (P < 0.05). Hyperbaric oxygenation after cell transplantation results in remarkable therapeutic angiogenesis and improves cardiac function by transplantation of vascular endothelial growth factor gene-modified bone marrow mesenchymal stem cells.

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