Edgell C J, Reisner H M, Graham J B
Br J Haematol. 1980 Dec;46(4):613-20. doi: 10.1111/j.1365-2141.1980.tb06019.x.
Hybrid somatic cell clones have been generated by fusing human vascular endothelial cells in primary culture to cells of four rodent lines. Factor VIII related antigen (VIIIR:Ag) was clearly demonstrable in the cultured endothelial cells, even when they had been co-cultured with rodent cells. But in none of 14 hybrid clones was VIIIR:Ag detectable. Isozyme analyses for human chromosome markers show that all the assayed human chromosomes were represented among the hybrids, and that various subsets of human chromosomes have been deleted from individual hybrid clones. It may be concluded, therefore, either that VIIIR:Ag production depends on a particular combination of human chromosomes not represented in any of the hybrids, or that the rodent cells contribute some agent which intracellularly blocks VIIIR:Ag expression.
通过将原代培养的人血管内皮细胞与四种啮齿类细胞系的细胞融合,已产生了杂种体细胞克隆。即使培养的内皮细胞与啮齿类细胞共同培养,也能清楚地检测到因子VIII相关抗原(VIIIR:Ag)。但在14个杂种克隆中均未检测到VIIIR:Ag。对人类染色体标记物的同工酶分析表明,所有检测的人类染色体都存在于杂种细胞中,并且各个杂种克隆中已缺失了人类染色体的不同亚群。因此,可以得出结论,要么VIIIR:Ag的产生取决于杂种细胞中未出现的特定人类染色体组合,要么啮齿类细胞产生了某种在细胞内阻断VIIIR:Ag表达的物质。