Boynton A L, Whitfield J F
In Vitro. 1976 Jul;12(7):479-84. doi: 10.1007/BF02796490.
In the presence of a normal (1.25 to 1.80 mM) calcium concentration, addition of fresh bovine calf serum or completely changing the medium induces proliferatively quiescent BALB/c 3T3 mouse cells in dense cultures to start a growth division cycle and initiate DNA synthesis about 12 hr later. Fresh, low-calcium (0.02 mM physiologically available) medium also causes cells to start a growth-division cycle. Howver, the development of such stimulated, calcium-deprived cells tops just before the expected time of initiation of DNA synthesis, which can then be rapidly induced by restoration of the normal calcium concentration. Simply raising the calcium concentration to nonphysiologically high levels (without otherwise altering the medium) can mimic the action of fresh serum or fresh whole medium by inducing some of the cells in proliferatively quiescent confluent concluent cultures to start a growth-division cycle and initiate DNA synthesis 22 hr later.
在正常钙浓度(1.25至1.80毫摩尔)存在的情况下,添加新鲜牛犊血清或完全更换培养基会诱导密集培养中增殖静止的BALB/c 3T3小鼠细胞开始生长分裂周期,并在约12小时后启动DNA合成。新鲜的低钙(生理可用浓度为0.02毫摩尔)培养基也会使细胞开始生长分裂周期。然而,这种受刺激的缺钙细胞的发育在预期的DNA合成起始时间之前就停止了,然后通过恢复正常钙浓度可以迅速诱导DNA合成。简单地将钙浓度提高到非生理高水平(不改变培养基的其他成分)可以模拟新鲜血清或新鲜全培养基的作用,诱导增殖静止的汇合培养物中的一些细胞开始生长分裂周期,并在22小时后启动DNA合成。