Tobey R A, Ley K D
J Cell Biol. 1970 Jul;46(1):151-7. doi: 10.1083/jcb.46.1.151.
Suspension cultures of Chinese hamster cells (line CHO) were grown to stationary phase (approximately 8-9 x 10(5) cells/ml) in F-10 medium. Cells remained viable (95%) for at least 80 hr in stationary phase, and essentially all of the cells were in G(1) Upon resuspension or dilution with fresh medium, the cells were induced to resume traverse of the life cycle in in synchrony, and the patterns of DNA synthesis and division were similar to those observed in cultures prepared by mitotic selection. Immediately after dilution, the rates of synthesis of RNA and protein increased threefold. This system provides a simple technique for production of large quantities of highly synchronized cells and may ultimately provide information on the biochemical mechanisms regulating cell-cycle traverse.
中国仓鼠细胞(CHO 系)的悬浮培养物在 F-10 培养基中生长至稳定期(约 8 - 9×10⁵ 个细胞/毫升)。细胞在稳定期至少 80 小时内保持活力(95%),并且基本上所有细胞都处于 G₁期。在用新鲜培养基重悬或稀释后,细胞被诱导同步重新进入生命周期,DNA 合成和分裂模式与通过有丝分裂选择制备的培养物中观察到的相似。稀释后立即,RNA 和蛋白质的合成速率增加了三倍。该系统提供了一种生产大量高度同步化细胞的简单技术,并最终可能提供有关调节细胞周期进程的生化机制的信息。