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重组腺病毒载体介导低氧诱导因子基因转染促进SD大鼠骨组织工程血管化的实验研究

HIF gene transfection therapy promotes revascularization of tissue-engineered bone in SD rat

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【作者】 白晓峰张霞李增健

【Author】 BAI Xiao-feng1,ZHANG Xia2,LI Zeng-jian1*(1.Department of Oromaxillofacial Surgery,School of Stomatology;2.Department of Anesthesiology,School of Stomatology,China Medical University,Shenyang 110002 China)

【机构】 中国医科大学口腔医学院口腔颌面外科中国医科大学口腔医学院麻醉科

【摘要】 目的评价重组腺病毒介导的低氧诱导因子基因导入是否具有促进SD大鼠骨组织工程的血管化的作用。方法通过重组低氧诱导因子腺病毒载体转染SD大鼠的骨髓基质细胞,然后将含有目的基因种子细胞与骨组织工程的支架材料藻酸钙复合成可注射性组织工程骨植入裸鼠背部皮下,应用Masson染色和SP免疫组化法观察异位成骨能力,检测构建组织的微血管密度计数(MVD)。结果动物实验显示,实验组新骨形成和新生血管形成良好,实验组的微血管化密度显著地高于对照组。结论低氧诱导因子基因导入有利于组织工程骨的新骨形成和再血管化。

【Abstract】 Objective To evaluate the use of adenoviral vector of HIF-1ɑ gene for enhancing revascularization of tissue-engineered bone in SD rats.Methods The rat bone marrow stromal cells isolated from the rats’femur were transfected with HIF-1ɑ gene in vitro.The genetically modified cells were then seeded into resorbable scaffold matrix to form tissue-engineered bone those were observed by Masson staining and CD 34 immunohistochemistry.Results Tissue constructs were implanted subcutaneously into nude rats successfully.Four weeks after surgery,blood supply to the bioengineered tissue in HIF-1ɑ gene modified group was much higher than that in the control groups,and microvascular density(MVD)around the tissue-engineered bone in the experiment group significantly increased compared with the control groups.Conclusion HIF-1ɑ gene therapy mediated by adenovirus may be useful for promoting revascularization of tissue-engineered bone and enhancing new bone formation.

【基金】 辽宁省教育厅高等学校科研资助项目(No.2008751)
  • 【文献出处】 解剖科学进展 ,Progress of Anatomical Sciences , 编辑部邮箱 ,2011年06期
  • 【分类号】R329
  • 【被引频次】1
  • 【下载频次】119
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