Leblond-Larouche L, Morais R
Can J Microbiol. 1976 Oct;22(10):1474-9. doi: 10.1139/m76-218.
Attempts have been made to keep in vitro, for extended periods of time, cultures of chick embryo fibroblasts transformed by the Schmidt-Ruppin strain of Rous sarcoma virus, subgroup D. Roller cultures of transformed chick cells kept in serum-deficient medium can be maintained without subcultivation for up to 6 months. The confluent cultures continuously release viruses and viable tumor cells into the medium. The released cells can be plated and have characteristics of growth and morphology which are relatively stable with time until the culture degenerates. Cells released at later stages of the culture produced substantially more viruses than those released earlier, suggesting that cell selection or differentiation occurs during long-term cultivation in low serum concentration. Long-term cultures of untransformed chick embryo fibroblasts can also be maintained in the same way. The release of viable cells by these confluent cultures, however, is negligible.
人们曾尝试在体外长时间培养由劳氏肉瘤病毒D亚组施密特-鲁平毒株转化的鸡胚成纤维细胞。在血清缺乏的培养基中进行转化鸡细胞的转瓶培养,无需传代即可维持长达6个月。汇合培养物持续向培养基中释放病毒和活的肿瘤细胞。释放出的细胞可以进行铺板培养,其生长和形态特征随时间相对稳定,直至培养物退化。培养后期释放的细胞比早期释放的细胞产生的病毒要多得多,这表明在低血清浓度的长期培养过程中发生了细胞选择或分化。未转化的鸡胚成纤维细胞的长期培养也可以用同样的方法维持。然而,这些汇合培养物释放的活细胞可以忽略不计。