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机构地区:[1]长春职业技术学院食品与生物技术分院,吉林省长春市130033 [2]吉林大学白求恩第三医院神经外二科,吉林省长春市130033 [3]吉林大学白求恩第三医院血管外科,吉林省长春市130033
出 处:《中国组织工程研究》2014年第29期4636-4641,共6页Chinese Journal of Tissue Engineering Research
摘 要:背景:胶质瘤的根除治疗至今仍是一大难题,抗血管生成治疗胶质瘤有望成为新的有效途径。目的:证实内皮抑素在体外对血管生长的抑制作用,为今后利用其抑制肿瘤生长奠定实验室基础。方法:取Wistar大鼠肝脏,提取mRNA后利用RT-PCR获取内皮抑素cDNA片段。碱裂解法小量提取质粒pcDNA3。重组质粒pcDNA3-Endo的构建。重组pcDNA3-Endo真核表达载体转染骨髓间充质干细胞。RT-PCR及Western Blot检测内皮抑素基因的表达。MTT法检测ECV-304细胞增殖抑制实验。体外实验共分成4个组:重组质粒组、空载质粒组、脂质体对照组及空白对照组。结果与结论:成功构建pcDNA3-Endo重组真核表达质粒,pcDNA3-Endo质粒能在体外有效转录并分泌内皮抑素基因,转染了外源pcDNA3-Endo质粒的ECV-304细胞增殖明显受到抑制。结果提示内皮抑素基因能在体外有效抑制血管内皮细胞的增殖。BACKGROUND: The eradication therapy of glioma is the major problem, and anti-angiogenesis therapy is a potential treatment of glioma. OBJECTIVE: To confirm the inhibiting effect of endostatin on angiogenesis in vitro, and to lay the foundation in inhibiting the growth of tumor by endostatin in the future. METHODS: Endostatin mRNA was extracted from the liver of Wistar rats by Trizol and endostatin cDNA was synthesized by RT-PCR. Endostatin cDNA and pcDNA3 were connected and pcDNA3-Endo racombined plasmid was constructed successfully. The recombinant pcDNA3-Endo was transfected into bone marrow mesenchymal stem cells by Lipofectamine. The expression of endostatin was identified by RT-PCR and western blot analysis. Endostatin proteinum activity was detected by ECV-304 cell proliferation inhibition experiment using MTT assay. The in vitro experiments were divided into four groups: recombinant plasmid group, vector plasmid group, liposome control group and blank control group. RESULTS AND CONCLUSION: PcDNA3-Endo eukaryon expression plasmid was constructed successfully. Endostatin gene can be transcribed and expressed effectively in vitro by pcDNA3-Endo plasmid. The growth of ECV-304 cell was inhibited obviously by pcDNA3-Endo. The growth of vascular endothelial cells can be inhibited obviously by endostatin gene.
关 键 词:内皮抑素类 内皮细胞 新生血管化 生理性 间质干细胞 组织构建 血管内皮细胞 内皮抑素 血管生成 人脐静脉血管内皮细胞 间充质干细胞 质粒 转染
分 类 号:R318[医药卫生—生物医学工程]
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