Otto A M, Nilsen-Hamilton M, Boss B D, Ulrich M O, Jimenez De Asua L
Proc Natl Acad Sci U S A. 1982 Aug;79(16):4992-6. doi: 10.1073/pnas.79.16.4992.
Prostaglandin (PG) E1 or E2 added at 2-1,000 ng/ml to quiescent cultures of Swiss 3T3 cells synergistically enhanced the rate of initiation of DNA replication stimulated by PGF2 alpha alone or with insulin. Neither PGD2 nor PGF1 alpha had any effect with PGF2 alpha. An increase in the rate of entry into S phase also occurred when PGE1 or PGE2 was added 8 or 15 hr after addition of PGF2 alpha. However, adding PGE1 and PGE2 together with PGF2 alpha did not further enhance the synergistic effect observed with PGE1 or PGE2 separately. The synergistic effect was also observed in stimulation of 2-deoxyglucose uptake but not in early changes of intracellular levels of cAMP. These results may be relevant in understanding the control of fibroblastic proliferation in wound healing and may provide an alternative mechanism for oncogenic transformation.
向处于静止状态的瑞士3T3细胞培养物中添加2 - 1000纳克/毫升的前列腺素(PG)E1或E2,可协同提高单独使用PGF2α或与胰岛素联合使用时刺激的DNA复制起始速率。PGD2和PGF1α与PGF2α一起使用均无任何效果。在添加PGF2α 8或15小时后添加PGE1或PGE2,进入S期的速率也会增加。然而,将PGE1和PGE2与PGF2α一起添加并不会进一步增强单独使用PGE1或PGE2时观察到的协同效应。在刺激2 - 脱氧葡萄糖摄取方面也观察到了协同效应,但在细胞内cAMP水平的早期变化中未观察到。这些结果可能与理解伤口愈合中纤维母细胞增殖的控制有关,并可能为致癌转化提供一种替代机制。