West China Journal of Stomatology

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Ultr asound - mediated microbubble destruction enhances exogenous gene expr ession in NIH3T3 cells in vitro

SUN Qin- feng1, LIU Yu2,YANG Pi- shan1, DU Fang1   

  1. 1. Dept. of Periodontology, School of Stomatology, Shandong University, Jinan 250012, China;2. Dept. of Periodontology, Stomatological Hospital, Medical College of Nanjing University,Nanjing 210008, China
  • Received:2008-04-25 Revised:2008-04-25 Online:2008-04-20 Published:2008-04-20
  • Contact: YANG Pi- shan,Tel:0531- 88382368

Abstract:

Objective To investigate the transfection efficiency of the recombinant human bone morphogenetic protein- 2(hBMP- 2) gene in targeted cells by ultrasound- mediated microbubble destruction. Methods NIH3T3 cells′ anabiosis was completed and went down to the 3rd or 4th generation, and cultured in 6 well plates. The cells were divided into 2 groups: Plasmid DNA and LipofectamineTM 2000 group(liposome group), plasmid DNA and ultrasound and microbubble group(ultrasound- mediated microbubble destruction group). Plasmid DNA was transfected into cells with liposome or ultrasound and microbubble. 24- 48 hours later, the transfection efficiency and the concentrations of hBMP- 2 were measured with fluoresence microscope and enzyme - linked immunosorbent assay(ELISA) respectively. The data were analyzed by curve fitting and t- test of SPSS 11.5. Results The transfection efficiency rate was(7.30± 1.58)% in liposome group, compared with (11.77±3.16)% in ultrasound- mediated microbubble destruction group(P< 0.05). The concentration of hBMP - 2 after transfection was (1 164.35 ±724.67)pg/mL in liposome group, versus (2 932.70±656.27)pg/mL in ultrasound- mediated microbubble destruction group(P<0.05). Conclusion Ultrasoundmediated microbubble destruction could significantly improve the transfection efficiency and expression of hBMP- 2 gene in NIH3T3 cells. It may provide a new and effective gene delivery system for gene therapy in periodontal regeneration.

Key words: ultrasound, microbubble, human bone morphogenetic protein- 2, gene therapy