Amitani K, Nakata Y
Clin Orthop Relat Res. 1977 Jan-Feb(122):315-24.
Osteosarcoma cells (BFO cell line) were successfully maintained in tissue culture for 3 years. BFO cells showed 100 per cent tumorigenicity by the isologous implantation, and almost the same histological features as the original BF osteosarcoma. BFO cells synthesize and secrete large quantities of alkaline phosphatase both in vitro (cell culture) and in vivo (tumor bearing mice). BFO cells showed a suppression in synthesizing the osteoinductive factor in vitro, but regained the capacity to synthesize it when implanted back into an isologous host. The cells showed rapid growth, a serum requirement, and no contact inhibition. Doubling time was 8.6 hours in a logarithmic growth phase. Cell cycle analyses by pulse labeling of 3H-thymidine was performed after synchronization of the cells by double treatment with an excess thymidine.
骨肉瘤细胞(BFO细胞系)在组织培养中成功维持了3年。通过同源植入,BFO细胞显示出100%的致瘤性,并且具有与原始BF骨肉瘤几乎相同的组织学特征。BFO细胞在体外(细胞培养)和体内(荷瘤小鼠)均能合成并分泌大量碱性磷酸酶。BFO细胞在体外合成骨诱导因子的能力受到抑制,但当重新植入同源宿主时又恢复了合成能力。这些细胞生长迅速,需要血清,且无接触抑制。在对数生长期,倍增时间为8.6小时。在用过量胸苷双重处理使细胞同步化后,通过3H-胸苷脉冲标记进行细胞周期分析。