Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (19): 3427-3432.doi: 10.3969/j.issn.1673-8225.2011.19.002

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In vitro differentiation of fetal bone marrow mesenchymal stem cells into islet beta like cells

Guo Jia-ning, Lei Jian-yuan, Li Yi, Chang Ji-wu   

  1. Department of Tumor Immunology, Tianjin Institute of Urology, Tianjin  300211, China
  • Received:2010-11-05 Revised:2011-01-17 Online:2011-05-07 Published:2011-05-07
  • Contact: Chang Ji-wu, Professor, Department of Tumor Immunology, Tianjin Institute of Urology, Tianjin 300211, China changjiwu2004@yahoo.com.cn
  • About author:Guo Jia-ning★, Master, Department of Tumor Immunology, Tianjin Institute of Urology, Tianjin 300211, China guojianing2005@163.com

Abstract:

BACKGROUND: There is no a mature program for identifying islet like cells differentiated from human bone marrow mesenchymal stem cells (BMSCs).
OBJECTIVE: To investigate the possibility of human fetal BMSCs differentiating into insulin-secreting cells in appropriate condition.
METHODS: The fetal BMSCs were co-cultured with fetal insulin cells on Transwell double-layer culture plate. In the control group, the BMSCs were cultured in culture medium containing islet cells. Morphological changes in fetal BMSCs and islet cells were analyzed under a phase contrast microscopy. The morphological changes and insulin secretions of BMSCs under the stimulation of fetal islet cells were detected by radioimmunoassay.
RESULTS AND CONCLUSION: The fetal BMSCs were isolated and purified, identical cell morphology liked plants spindle-like arrangement. Fetal islet cells were confirmed by panccreatic β endocrine cells under electron microscopy. The undifferentiated BMSCs exhibited were adherent and long spindle-shaped cells. After induction, cells gradually became round and formed clusters. Cells secreted abundant insulin and formed islet-like cell clusters that exhibited positive dithizone staining and immunocytochemical staining at 9 days. No insulin was detected in the control group. It is indicated that fetal BMSCs have the potentiality to differentiate into insulin-producing cells in appropriate condition.

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