Balk S D, Morisi A, Gunther H S
Proc Natl Acad Sci U S A. 1984 Oct;81(20):6418-21. doi: 10.1073/pnas.81.20.6418.
Cultured chicken heart mesenchymal cells are proliferatively quiescent at low densities in medium containing plasma at 10%. Mitogenic hormones like epidermal growth factor and insulin-like growth factors cause these cells to proliferate very actively, as does infection with avian sarcoma viruses, erythroblastosis virus, or myelocytomatosis virus. We have found that the combination of phorbol 12-myristate 13-acetate (PMA), ionomycin or ouabain, and raised extracellular magnesium, likewise, causes these cells to proliferate very actively. Although these agents have no significant effect when acting singly, the combination of PMA at 100 ng/ml and 0.5 microM ionomycin induces a 6-fold increase in cell number at 4 days, and the combination of PMA, ionomycin, and 5.6 mM magnesium induces 12-fold multiplication. Likewise, PMA plus 1 microM ouabain induces 3-fold multiplication, whereas the combination of PMA, ouabain, and magnesium induces 6-fold multiplication. The tumor promoter PMA, like diacylglycerol released by breakdown of plasma membrane phosphatidylinositol diphosphate, is known to activate the serine- and threonine-specific intracellular enzyme kinase C. The divalent cation ionophore ionomycin is known to carry calcium into cells down an electrochemical gradient, and the Na+,K+-ATPase inhibitor ouabain appears to elevate intracellular calcium by means of a sodium-mediated exchange mechanism. Magnesium, like calcium, is known to enter cells passively down an electrochemical gradient and to be involved in the regulation of many key intracellular reactions. Our findings with PMA, ionotropes, and magnesium support a hypothesis that diacylglycerol-mediated activation of kinase C plus cellular divalent cation influx and/or mobilization, caused by the action of mitogenic hormones or the protein products of onc genes, are key events in the initiation of cell replication.
培养的鸡心脏间充质细胞在含有10%血浆的培养基中低密度时处于增殖静止状态。有丝分裂激素如表皮生长因子和胰岛素样生长因子会使这些细胞非常活跃地增殖,感染禽肉瘤病毒、成红细胞增多症病毒或骨髓细胞瘤病毒也会如此。我们发现,佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)、离子霉素或哇巴因与细胞外镁离子浓度升高的组合同样会使这些细胞非常活跃地增殖。尽管这些试剂单独作用时没有显著效果,但100 ng/ml的PMA与0.5 μM离子霉素的组合在4天时会使细胞数量增加6倍,而PMA、离子霉素和5.6 mM镁离子的组合会使细胞增殖12倍。同样,PMA加1 μM哇巴因会使细胞增殖3倍,而PMA、哇巴因和镁离子的组合会使细胞增殖6倍。肿瘤促进剂PMA,就像质膜磷脂酰肌醇二磷酸分解产生的二酰基甘油一样,已知能激活丝氨酸和苏氨酸特异性细胞内酶激酶C。二价阳离子载体离子霉素已知能使钙离子沿电化学梯度进入细胞,而Na +,K + - ATP酶抑制剂哇巴因似乎通过钠介导的交换机制提高细胞内钙浓度。镁离子与钙离子一样,已知能沿电化学梯度被动进入细胞并参与许多关键细胞内反应的调节。我们关于PMA、离子载体和镁离子的研究结果支持了这样一种假说,即由有丝分裂激素或癌基因的蛋白质产物作用引起的二酰基甘油介导的激酶C激活加上细胞二价阳离子内流和/或动员是细胞复制起始的关键事件。