Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (14): 2524-2529.doi: 10.3969/j.issn.1673-8225.2012.14.011

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Effects of co-culture system on Bmi-1 expression in bone marrow mesenchymal stem cells

Yang Rui-nian, Liu Liu, Wang Fu-ke, Zhao De-ping   

  1. Department of Head and Neck Surgery, First Affiliated Hospital of Kunming Medical College, Kunming 650032, Yunnan Province, China
  • Received:2011-12-27 Revised:2012-01-22 Online:2012-04-01 Published:2012-04-01
  • Contact: author: Liu Liu, Professor, Doctoral supervisor, Department of Head and Neck Surgery, First Affiliated Hospital of Kunming Medical College, Kunming 650032, Yunnan Province, China liuliu3939@126.com
  • About author:Yang Rui-nian☆, Studying for doctorate, Physician, Department of Head and Neck Surgery, First Affiliated Hospital of Kunming Medical College, Kunming 650032,Yunnan Province, China 13888425351@ 163.com
  • Supported by:

    the National Natural Science Foundation of China, No.30960388*; 81160239*

Abstract:

BACKGROUND: Vascular endothelial cells can promote osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and provide nutritional support for growth and proliferation of BMSCs.
OBJECTIVE: To investigate the effects of human umbilical vein vascular endothelial cells (hUVECs) in a co-culture system on morphology, growth and differentiation of human BMSCs, and Bmi-1 gene expression in cells.
METHODS: Based on the co-culture system of cells, a simple culture group (hBMSCs group) and a combined culture group (BMSCs + hUVECs group) were established. On days 4, 6, 8, 10, cell morphology was observed and cells were counted for drawing cell growth curves; in addition, Bmi-1 gene expression in cells was detected in each group using real-time quantitative fluorescent PCR.
RESULTS AND CONCLUSION: At each time point, compared with hBMSCs group, cells exhibited multiple morphological changes, some cells connected together in the latter stage, and osteogenic differentiation was more obvious in the BMSCs + hUVECs group. At each time point, cell number and Bmi-1 expression in the BMSCs + hUVECs group were significantly greater than in the BMSCs group. The BMSCs + hUVECs group showed a better compatibility compared with the hBMSCs group. These findings suggest that hUVECs promote the proliferation of hBMSCs in the co-culture system, and increase Bmi-1 expression in hBMSCs, thereby affecting aging and proliferative capacity of hBMSCs.

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