Rozengurt E, Collins M K, Keehan M
J Cell Physiol. 1983 Sep;116(3):379-84. doi: 10.1002/jcp.1041160316.
Addition of prostaglandin E1 (PGE1) to quiescent cultures of Swiss 3T3 cells rapidly elevates the intracellular levels of cAMP and increases the activity of adenylate cyclase in particulate fractions of these cells. In the presence of insulin, PGE1 stimulates the reinitiation of DNA synthesis. Both effects (increase in cellular cAMP and stimulation of DNA synthesis) are markedly potentiated by 1-methyl-3-isobutyl xanthine (IBMX) or by 4-(3-butoxy-4 methoxy benzyl)-2-imidazolidine (Ro 20-1724), both of which are potent inhibitors of cyclic nucleotide phosphodiesterase activity. In the presence of 50 microM IBMX, PGE1 caused a dose-dependent increase in cAMP levels and in [3H]thymidine incorporation into acid-insoluble material at concentrations (5-50 ng/ml) that are orders of magnitude lower than those used in previous studies (50 micrograms/ml) to demonstrate growth-inhibitory effects. Thus, the inhibitory effects produced by adding high concentrations of PGE1 on the initiation of DNA synthesis in Swiss 3T3 cells are not mediated by cAMP and should be regarded as nonspecific. In contrast, the mitogenic activity of PGE1 parallels its ability to increase the intracellular levels of cAMP. The findings support the proposition that a sustained increase in the level of this cyclic nucleotide acts as a mitogenic signal for confluent and quiescent Swiss 3T3 cells.
向瑞士3T3细胞的静止培养物中添加前列腺素E1(PGE1)可迅速提高细胞内cAMP水平,并增加这些细胞微粒部分中腺苷酸环化酶的活性。在胰岛素存在的情况下,PGE1刺激DNA合成重新启动。1-甲基-3-异丁基黄嘌呤(IBMX)或4-(3-丁氧基-4-甲氧基苄基)-2-咪唑烷(Ro 20-1724)可显著增强这两种作用(细胞内cAMP增加和DNA合成刺激),这两种物质都是环核苷酸磷酸二酯酶活性的有效抑制剂。在50 microM IBMX存在的情况下,PGE1在浓度(5-50 ng/ml)下导致cAMP水平和[3H]胸苷掺入酸不溶性物质呈剂量依赖性增加,该浓度比先前研究中用于证明生长抑制作用的浓度(50微克/ml)低几个数量级。因此,添加高浓度PGE1对瑞士3T3细胞DNA合成起始产生的抑制作用不是由cAMP介导的,应被视为非特异性的。相比之下,PGE1的促有丝分裂活性与其增加细胞内cAMP水平的能力平行。这些发现支持了这样一种观点,即这种环核苷酸水平的持续增加作为汇合和静止的瑞士3T3细胞的促有丝分裂信号。