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血管内皮细胞生长因子基因在骨髓间充质干细胞中的表达

于音1,赵刚1,许侃1,房学迅2,赵丽2   

  1. (1.吉林大学第一医院神经外科,吉林 长春 130021;2.吉林大学药学院生物工程教研室,吉林 长春 130021)
  • 收稿日期:2007-01-11 修回日期:1900-01-01 出版日期:2007-11-28 发布日期:2007-11-28
  • 通讯作者: 赵刚

Expression of vascular endothelial growth factor gene inbone marrow mesenchymal stem cells

YU Yin1,ZHAO Gang1,XU Kan1,FANG Xue-xun2,ZHAO Li-chun2   

  1. 1.Department of Neurosurgery,First Hospital,Jilin University,Changchun 130021,China;2.Department of Bioengineering,School of Pharmacy,Jilin University,Changchun 130021,China
  • Received:2007-01-11 Revised:1900-01-01 Online:2007-11-28 Published:2007-11-28
  • Contact: ZHAO Gang

摘要: 目的: 研究血管内皮细胞生长因血管内皮细胞生长因子基因在骨髓间充质干细胞中的表达子(VEGF)基因转染兔骨髓间充质干细胞(MSCs)后的表达和分泌情况,为构建一种血供丰富、成骨能力及骨块存活能力更强的组织工程化人工颅骨奠定实验室基础。方法: 应用基因重组技术,将VEGF165基因全长片段克隆于真核表达载体pcDNA3中,构建pcDNA3-VEGF165真核表达质粒;应用阳离子脂质体介导的基因转染技术,将pcDNA3-VEGF165真核表达质粒转染进入兔骨髓间充质干细胞中;利用RT-PCR及Western blotting方法检测VEGF基因在MSCs中的表达情况。结果: 构建的真核表达质粒-pcDNA3-VEGF165经双酶切后分别在5 400 bp和600 bp处出现条带,证实其构建成 功;成功进行了兔MSCs的原代及传代培养,并建立兔MSCs库,原代细胞初为淋巴细胞样小圆细胞,此后逐渐变为圆形、梭形或不规则形,而传代细胞则变为形态更均一、排列更有序的成纤维细胞样细胞;RT-PCR及Western blotting检测到瞬时转染后的细胞有VEGF mRNA及VEGF蛋白的表达。结论: pcDNA3-VEGF165真核表达质粒通过脂质体能够有效转染兔MSCs,转染后的细胞具有表达VEGF蛋白的能力。

关键词: 血管, 内皮生长因子, 骨髓祖代细胞, 转染

Abstract: To study the vascular endothelial growth factor (VEGF) expression and secretion of mesenchymal stem cells (MSCs) of rabbit transfected with pcDNA3-VEGF165 expression plasmid in order to construct a kind of tissue engineering artificial skull with more blood supply.MethodsBy gene reconstruction method,the VEGF165 gene was cloned into eukaryotic expression plasmid pcDNA3 and recombined eukaryotic expression plasmid pcDNA3-VEGF165 was constructed;By lipofectamine transfection method,pcDNA3-VEGF165 expression plasmid was transfected into MSCs of rabbit;By RT-PCR and Western blotting methods,the VEGF mRNA expression and VEGF protein secretion in the MSCs were detected. Results Recombined eukaryotic expression plasmid pcDNA3-VEGF165 was confirmed to be true by double enzyme digestion,two strips came to appear in 5400 bp and 600 bp of gelose electrophoresis and their sizes accorded with pcDNA3 plasmid and VEGF165 accordingly;Primarily cultured and subcultured MSCs of rabbit were successfully performed and the MSCs storehouse of rabbit was established,primary MSCs presented lymphoid form at first and then the morphology of them became circulara,polygonal or irregular forms,they were more and more like fibroblastic cells after subcultured cultivation.The expressions of VEGF mRNA and VEGF protein in the MSCs were found after transiently transfection by RT-PCR and Western blotting methods. Conclusion Recombined eukaryotic expression plasmid pcDNA3-VEGF165 can be transfected into MSCs of rabbit effectively by lipofectamine and the VEGF expression can be detected in the MSCs after transfection.

Key words: vascular, endothelial growth factors, myeloid progenitor cells, transfection

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  • Q786