【摘要】 目的建立肝癌细胞微细胞介导染色体转移方法,为肝癌转移抑制基因的染色体功能定位建立技术平台。方法人单染色体供体细胞通过微核化、出核、融合步骤将随机标记有耐药neo基因的正常人8号染色体导入到大鼠肝癌高转移细胞系C5F中,对微细胞杂交克隆进行药物筛选和单细胞克隆,并用序列标签位点-PCR和全染色体涂染荧光原位杂交方法验证人染色体转移的结果。结果获得具有G418和HAT双重抗性的微细胞杂交细胞,通过单细胞分离克隆方法获得15个具有双重抗性的微细胞杂交克隆,序列标签位点-PCR结果发现导入染色体的随机片段丢失,全染色体涂染荧光原位杂交结果发现导入的人8号染色体与大鼠染色体发生了稳定的重组。结论成功建立微细胞介导的染色体转移技术,为肝癌转移抑制基因的染色体功能定位奠定了技术基础。更多还原

【Abstract】 Objective In order to seek the functional evidence that there could be metastatsis suppressor gene for liver cancer on human chromosomes, the objective of this study is to establish a method of microcell mediated chromosome transfer (MMCT). Methods Human chromosome 8 randomly marked with neo gene was introduced into highly metastatic rat liver cancer C5F cell line by treating the single human chromosome donor cells with sequential steps of micronucleation, enucleation and microcell fusion. Double selections of G418 and HAT were applied to screen positive microcell hybrids, which were cloned by single cell isolation. Microcell hybrid clones were confirmed by STS-PCR and WCP-FISH. Results Microcell hybrids resistant to HAT and G418 were obtained, from which 15 clones were obtained by single-cell isolation cloning. STS-PCR and WCP-FISH proved that human chromosome 8 had been successfully introduced into rat liver cancer cell line C5F. The human chromosome 8 introduced into C5F was found to have random loss of chromosome fragments by STS-PCR and consistent recombination with rat chromosome by WCP-FISH. Conclusion The successful introduction of human chromosome into highly metastatic rat liver cancer cell line has established the technical basis for functional localization of metastasis suppressor gene(s) for liver cancer on human chromosomes.更多还原