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作 者:唐洁[1] 胡娅莉[1] 刁振宇[1] 孙海翔[1] 颜桂军[1] 陈林君[1] 张艳青[1]
机构地区:[1]南京大学医学院附属鼓楼医院妇产科,210008
出 处:《中华围产医学杂志》2009年第6期425-429,共5页Chinese Journal of Perinatal Medicine
基 金:国家自然科学基金项目(30872775);江苏省兴卫工程领军人才项目(LJ200628);江苏省医学分子技术重点实验室(BM2007208);江苏省生殖健康公共技术服务中心(BM2008151)
摘 要:目的构建腺病毒介导的小鼠可溶性endoglin(sEng)和可溶性血管内皮生长因子受体-1(sFlt-1)重组蛋白,观察其对内皮细胞管化及滋养细胞迁移的影响。方法提取小鼠胎盘组织总RNA,通过RT—PCR获得sEng和sFlt-1 cDNA,插入到穿梭载体pAdTrack—CMV中,获得pATC-sEng和pATC—sFh-1质粒,转化其至pAdeasy-1受体菌,选阳性克隆转染293A细胞,获得Ad/sEng和Ad/sFlt-1,制备高滴度病毒液。用病毒感染COS7细胞,检测sEng和sFlt-1蛋白表达,并通过成管和划痕实验观察两种蛋白对人脐静脉血管内皮细胞(HUVEC)管化和Bewo细胞迁移的影响。结果成功获得sEng和sFlt-1重组腺病毒,其滴度分别为2.2×10^11pfu/ml和2.0X10^11pfu/ml。感染COS7细胞后,sEng和sFlt-1蛋白均较高表达,并能抑制HUVEC管化及Bewo细胞迁移,两者有协同作用。结论构建的腺病毒介导的小鼠sEng和sFlt-1重组蛋白对血管生成和滋养细胞迁移有明显抑制作用。Objective To construct the recombinant adenovirus Ad/sEng and Ad/sFlt-1, and investigate their effects on angiogenesis and the migration of human umbilical vein endothelial cells (HUVEC) and trophoblast. Methods The sEng and sFlt-1 cDNA were obtained from mouse placenta by RT-PCR, which were inserted into the shuttle plasmid pAdTrack-CMV. After confirmation by endonuclease and sequencing, we transferred them into Escherichia coll. BJ5183- AD-1 cells were applied to obtain the homologous recombinants, which were transfected into 293A cells to obtain Ad/sEng and Ad/sFlt-1, and COS7 cells were infected with them. The expressions of sFlt-I and sEng were detected by Western blot. The effects of both proteins on HUVEC tube formation and BeWo migration were investigated. Results High titers of Ad/sEng and Ad/sFlt-1 were obtained (2.2 ×10^11 pfu /ml and 2. 0× 10^11 pfu/ml, respectively) and both sFlt1 and sEng proteins were efficiently expressed, which inhibited the HUVEC tube formation and BeWo cell migration. Conclusions Adenovirus mediated mouse sFlt-1 and sEng has been constructed and expressed successfully in vitro with inhibitory effects on angiogenesis and the migration of HUVEC and trophoblast.
关 键 词:先兆子痢 细胞内信号肽和蛋白质类 血管内皮生长因子受体1 重组蛋白质类 腺病毒科
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