Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (19): 3442-3446.doi: 10.3969/j.issn.1673-8225.2012.19.005

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Effects of hypoxia on proliferation and migration of rat bone marrow mesenchymal stem cells

Wang Li-wei, Zhao Yu, Huang Xu, Huang Wen   

  1. Department of Vascular Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
  • Received:2011-10-28 Revised:2011-12-29 Online:2012-05-06 Published:2012-05-06
  • Contact: Huang Wen, M.D., Associate chief physician, Associate professor, Department of Vascular Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China dhuangwen@hotmail.com Corresponding author: Zhao Yu, Master, Professor, Doctoral supervisor, Department of Vascular Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
  • About author:Wang Li-wei★, Master, Department of Vascular Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China 439915562@qq.com
  • Supported by:

    Research Program of Chongqing Education Commission, No. KJ090320*

Abstract:

BACKGROUND: Studies have demonstrated that turnover of transplanted bone marrow mesenchymal stem cells (BMSCs) with poor differentiation potential in ischemic environment greatly influences curative effects.
OBJECTIVE: To investigate the effects of hypoxia changes on proliferation and homing ability of rat BMSCs. 
METHODS: Sprague-Dawley rat BMSCs were isolated and then cultured under atmosphere of 1% O2 (hypoxia group) and 20% O2 (normoxia group) respectively for 0-7 days. Cells for Transwell chamber migration were classified into four groups by oxygen concentration at culture and migration: 1%O2 culture and 1%O2 migration, 20%O2 culture and 1%O2 migration, 1%O2 culture and 20%O2 migration, 20%O2 culture and 20%O2 migration. Migrated cells were counted. Protein levels of integrin β1 and intercellular adhesion molecule-1 in BMSCs cultured under different concentrations of oxygen were detected by western blot.
RESULTS AND CONCLUSION: Migration and proliferation abilities of BMSCs were enhanced under the atmosphere of 1%O2 and the abilities were weakened under the atmosphere of 20%O2 (P < 0.05). Integrin β1 expression in BMSCs was increased under the atmosphere of 1%O2 (P < 0.05). These findings suggest that 1% O2 enhances the proliferation and migration abilities of rat BMSCs after transplantation.

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