期刊文献+

pcDNA3-hBMP2转染兔骨髓基质细胞前后生长特性的研究 被引量:2

Comparative Study on Main Biological Characteristics of Pre-transfected Rabbit Marrow Stromal Cells and Post-transfected with pcDNA3-hBMP2
原文传递
导出
摘要 目的观察pcDNA3-hBMP2转染兔骨髓基质细胞前后的生长特性变化,为骨组织工程的种子细胞选择打下基础。方法抽取成年雄性新西兰大白兔髂骨骨髓,密度梯度离心获得骨髓基质细胞,培养传至第5代,按处理方法分为常规培养液组(A组),pcDNA3-hBMP2转染组(B组)。观察原代MSC及第5代的细胞形态等生长特性并与转染组进行比较。结果原代MSCs为短梭形,簇形生长,传代细胞呈长梭形,旋涡形生长。转染组细胞72 h后表达BMP2,瞬间表达为100%。转染细胞未经筛选培养4周细胞形态发生较明显地变化,细胞生长周期改变。结论pcDNA3-hBMP2成功转染兔骨髓基质细胞并改变其生物学特性。 Objective To observe main biological characteristic and changes before and after MSCs were transfected with pcDNA3 - hBMP2. Methods MSCs from an adult New Zealand white rabbit were isolated and cultivated. MSCs were divided into two groups. Group A was transfected with pcDNA3 - hBMP2 and group B was not transfected as control group. Immunohistochemical staining was used for detecting BMP2 expressing 2 days after transfection. The cell morphological changes, cell divide index and cell cycle were observed after transfection. Results Rabbit MSCs could be successfully transfected by pcDNA3 - hBMP2 through medium fugene 6 and express BMP2. Primary MSCs proliferated as short spindle shape, while post - transfected MSCs showed triangle- shape, and transletted- cells had significant difference in cell cycle and cell divide index. Conclusion Rabbit MSCs can be successfully transfected by pcDNA3 - hBMP2 and after transfection many biological characteristics are significantly changed in this study.
出处 《中国骨与关节损伤杂志》 2009年第1期52-54,共3页 Chinese Journal of Bone and Joint Injury
基金 国家自然基金资助项目(30672125)
关键词 组织工程 骨髓基质细胞 生长特性 Tissue engineering Bone marrow stromal cells Biological characteristics
  • 相关文献

参考文献1

二级参考文献12

  • 1Lou J, Xu F, Merkel K, et al. Gene therapy: adenovirus-mediated human bone morphogenetic protein-2 gene transfer induces mesenchymal progenitor cell differentiation in vitro,bone formation in vivo. J Orthop Res,1999,17:43-50.
  • 2Lieberman JR, Daluiski A, Stevenson S, et al. The effect of regional gene therapy with bone morphogenetic protein-2-producing bone-marrow cells on the repair of segmental femoral defects in rats. J Bone and Joint Surg,1999,81-A:905-917.
  • 3Tsuchida H, Hashimoto J, Lou J, et al. Engineered allogeneic mesenchymal stem cells repair femoral segmental defect in rats. J Orthop Res,2003,21:44-53.
  • 4Riew KD, Wright NM, Lou J, et al. Induction of bone formation using a recombinant adenoviral vecter carrying the human BMP-2 gene in a rabbit spinal fusion model. Calcified Tissue International, 1998,63:357-360.
  • 5Reddi AH. Bone morphogenetic proteins: from basic science to clinical applications J Bone and Joint Surg, 2001, 83A (S1): 1-6.
  • 6John MW, Vicki R. Bone morphogenetic protein and bone morphogenetic protein gene family in bone formation and repair. Clin Orthop,1998,346:26-37.
  • 7Baltzer AWA, Lattermann C, Whalen JD, et al. Potential role of direct adenoviral gene transfer in enhancing fracture repair. Clin Orthop,2000,379:S120-S125.
  • 8Blokhuis TJ, Wippermann BW, Haarman HJ,et al. Resorbable calcium phosphate particles as a carrier material for bone marrow in an ovine segmental defect. J Biomed Mater Res,2000,51:369-375.
  • 9Petite H, Viateau V, uillemin G, et al. Tissue-engineered bone regeneration. Nat Biotechnol,2000,18:929-930.
  • 10Kon E, Muraglia A, Quarto R, et al. Autologous bone marrow mesenchymal stem cells loaded onto porous hydroxyapatite ceramic accelerate bone repair in critical-size defects of sheep long bones. J Biomed Mater Res,2000,49:328-337.

共引文献24

同被引文献37

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部