Mitaka T, Sattler G L, Pitot H C
Department of Oncology, Medical School, University of Wisconsin, Madison 53706.
In Vitro Cell Dev Biol. 1991 Jul;27A(7):549-56. doi: 10.1007/BF02631285.
Bicarbonate in the culture medium is essential for DNA synthesis of primary cultured rat hepatocytes stimulated by epidermal growth factor (EGF). When primary cultured hepatocytes in supplemented Leibovitz L15 medium were placed in a 100% air incubator, no increase in DNA synthesis was observed even after stimulation by EGF. However, when these cells were cultured with NaHCO3 and EGF and placed in a 5% CO2:95% air incubator, a stimulus of DNA synthesis more than 10-fold greater than in cultures in air only was seen, and many mitotic figures could be identified. Furthermore, NaHCO3 added to supplemented DMEM/F12 medium enhanced the DNA synthesis of primary cultured rat hepatocytes in this medium. The ideal pH of the medium for DNA synthesis of cultured hepatocytes was in the range of 7.6 to 8.0. A dose response of NaHCO3 in several media showed that DNA synthesis of the cells increased as the concentration of NaHCO3 increased and that 25 to 30 mM NaHCO3 in the medium was optimal for the replication of DNA by primary cultured rat hepatocytes.
培养基中的碳酸氢盐对于表皮生长因子(EGF)刺激的原代培养大鼠肝细胞的DNA合成至关重要。当将补充了Leibovitz L15培养基的原代培养肝细胞置于100%空气培养箱中时,即使在EGF刺激后,也未观察到DNA合成增加。然而,当这些细胞与NaHCO3和EGF一起培养并置于5% CO2:95%空气培养箱中时,观察到DNA合成的刺激比仅在空气中培养的细胞高出10倍以上,并且可以识别出许多有丝分裂图。此外,添加到补充的DMEM/F12培养基中的NaHCO3增强了该培养基中原代培养大鼠肝细胞的DNA合成。培养肝细胞DNA合成的理想培养基pH值在7.6至8.0范围内。几种培养基中NaHCO3的剂量反应表明,细胞的DNA合成随着NaHCO3浓度的增加而增加,并且培养基中25至30 mM的NaHCO3对于原代培养大鼠肝细胞的DNA复制是最佳的。