摘要
利用逆转录病毒载体LXSN构建了含有完整编码TNFcDNA的重组逆转录病毒质粒pLXSN-tnf,用Lipofectamine将重组质粒导入病毒包装细胞pA317,经G418筛选培养获得抗性克隆,用NIH3T3细胞测定病毒滴度,获得滴度为5×105CFU/ml的细胞克隆。利用病毒上清液感染大鼠胶质瘤细胞系C6,得到G418抗性克隆细胞C6pLXSN-tnf,经PCR检测,TNFcDNA完整地整合在细胞基因组中。测定C6pLXSN-tnf细胞上清中TNF的生物活性,结果显示TNF有相对稳定的表达(48~180U/ml106cells/24h)。实验还显示经TNF基因转导的C6pLXSN-tnf细胞生长速度较之亲本肿瘤细胞C6明显下降,基因修饰后的肿瘤细胞在Wistar大鼠体内形成肿瘤的能力明显受到抑制。进一步用超离心法浓缩病毒对胶质瘤移植模型进行了体内治疗研究。
AbstractOne recombinant plasmid pLXSN-tnf was constructed with tumornecrosis factor alpha ( TNFa ) cDNA and retroviral vector pLXSN.Afteridentified by restriction endonuclease digestion. pLXSN-tnf was intro-duced into packaging cell line PA317 by lipofectamine transfectionmethod. Several G418-resistant colonies were obtained and the virustiter in supernatant of the colonies were determined by NIH3T3 cells.
出处
《中国实验动物学报》
CAS
CSCD
1996年第1期57-63,共7页
Acta Laboratorium Animalis Scientia Sinica