Chinese Journal of Tissue Engineering Research ›› 2016, Vol. 20 ›› Issue (19): 2777-2782.doi: 10.3969/j.issn.2095-4344.2016.19.006

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Simvastatin effects on the expressions of specific osteogenic genes in bone marrow stromal stem cells

Liu Hao1, Zhang Yan1, Liu Jia-yin1, Liu Guang-yuan1, Zhang Ke-zhong1, Zhang Guo-bin2, Xing Lei1,Tian Fa-ming3   

  1. 1Affiliated Hospital, 2Graduate School, 3Medical Research Center, North China University of Science and Technology, Tangshan 063000, Hebei Province, China
  • Received:2016-03-17 Online:2016-05-06 Published:2016-05-06
  • Contact: Tian Fa-ming, M.D., Associate professor, Master’s supervisor, Medical Research Center of North China University of Science and Technology, Tangshan 063000, Hebei Province, China
  • About author:Liu Hao, Master, Attending physician, Affiliated Hospital of North China University of Science and Technology, Tangshan 063000, Hebei Province, China
  • Supported by:

    the Natural Science Foundation of Hebei, No. H2013209255; the Scientific Research Project of Hebei Universities and Colleges, No. QN20131007; Tangshan Key Laboratory Project of Geriatric Medicine, No. 14140221B

Abstract:

BACKGROUND: Previous studies have demonstrated that simvastatin that can promote osteogenic differentiation of bone marrow stromal stem cells in vitro, is likely to be a new osteogenic drug. While it is still unknown whether there is time-dependent stimulation of simvastatin on the expressions of bone morphogenetic protein 2 and collagen type I.
OBJECTIVE: To investigate the expressions of bone morphogenetic protein 2 and collagen type I in rat bone marrow stromal stem cells in vitro stimulated by simvastatin at different time points.
METHODS: Passage 1 bone marrow stromal cells were divided into control and simvastatin group, followed by cultured in osteogenic differetiation medium with or uithout 10-7 mol/L simvastatin. After 7-day intervention, expression of alkaline phosphatase was detected in passage 3 cells. Passage 4 cells were divided and cultured as described above, and afterwards, RNA and proteins were extracted at 12 and 36 hours to detect the expressions of bone morphogenetic protein 2 and collagen type I using real-time PCR and western blot assay.
RESULTS AND CONCLUSION: Both two groups could express alkaline phosphatase, while the rate of positive cells significantly increased in the simvastatin group compared with the control group (P < 0.05); at 12 and 36 hours after intervention, mRNA expressions of bone morphogenetic protein 2 and collagen type I in the simvastatin group were significantly higher than those in the control group (P < 0.05). Besides, western blot assay showed: at both 12 and 36 hours, simvastatin significantly enhanced the expression of bone morphometric protein 2, while the expression of collagen type I significantly increased at 12 hours (P < 0.05), but not at 36 hours. In conclusion, simvastatin can promote the expressions of bone morphometric protein 2 and collagen type I in rat bone marrow stromal cells, with more favorable outcomes after 12-hour treatment.

 

 

Key words: Bone Marrow, Mesenchymal Stem Cells, Simvastatin, Bone Morphogenetic Proteins, Collagen Type I, Tissue Engineering

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