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作 者:彭冬君[1] 尹燕华[1] 王宇哲[1] 孙军[1] 宗义强[1] 屈伸[1]
机构地区:[1]华中科技大学同济医学院基础医学院生物化学与分子生物学系,武汉市430030
出 处:《医学分子生物学杂志》2004年第2期94-97,共4页Journal of Medical Molecular Biology
摘 要:目的研究TRAIL基因与鸡贫血病毒vp3基因在体外协同诱导肝癌细胞系HepG2凋亡的作用。方法从人外周血淋巴细胞总RNA中扩增出TRAIL基因的cDNA序列,构建含TRAIL基因的真核表达重组体,与鸡贫血病毒vp3基因在体外共转染HepG2细胞,研究其协同诱导HepG2细胞凋亡作用。结果 单独转染TRAIL基因与vp3基因均可诱导HepG2细胞凋亡;将两种基因共转染HepG2细胞,发现其凋亡率明显增加。结论TRAIL基因与vp3基因在诱导HepG2细胞凋亡中存在正协同效应。Objective To explore the hepatoma cell line HepG2 apoptosis-induced effect of TRAIL cooperating with vp3 in vitro. Methods Eukaryotic expression vector for TRAIL cDNA acquired from human lymphocytes was constructed. After co-transfecting with vp3 gene, HepG2 apoptosis-induced effect was observed. Results TRAIL and vp3 gene could induce apoptosis of HepG2 cells in vitro, and enhanced effect was observed by co-transfecting TRAIL with vp3 gene. Conclusion Positive-cooperative effect of TRAIL and vp3 exist in apoptosis-induction of HepG2 cells.
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