Peleg S, Lindner H R
Mol Cell Endocrinol. 1980 Dec;20(3):209-18. doi: 10.1016/0303-7207(80)90036-2.
The effect of oestrogen and progesterone on prostaglandin synthesis and on DNA synthesis by rat decidual cells was studied in a culture system. The cells were explanted from deciduoma either during the proliferation phase (namely on the 5th day of leukocytic smear, Day L5:"L5 cells") or during the maintenance phase ("L8 cells") and examined on the second day of culture. Oestradiol-17 beta (7 X 10(-11) M) and progesterone (6 X 10(-8) M) significantly inhibited accumulation of PGE by cells explanted on Day L5: L8-cell cultures showed no significant response to oestradiol and the progesterone effect was markedly reduced. Progesterone stimulated [3H]thymidine incorporation into cells explanted on Day L5, but had no effect on L8-cultures. Other inhibitors of PG synthesis, namely cortisol, flufenamic acid and indomethacin, also had a stimulatory effect on DNA synthesis by L5 cells. PGE2 (5-10 micrograms/ml) inhibited DNA synthesis in control, indomethacin-treated and progesterone-treated L5-cell cultures, suggesting that the progesterone-induced stimulation of DNA synthesis may be in part be due to its inhibitory effect on PGE accumulation by decidual cells. The possibility is discussed that during the proliferation phase of decidual development in vivo, the rate of DNA synthesis may be influenced by steroid-induced changes in PGE content of the tissue.
在一个培养系统中研究了雌激素和孕酮对大鼠蜕膜细胞前列腺素合成及DNA合成的影响。细胞分别取自处于增殖期(即白细胞涂片第5天,L5日:“L5细胞”)或维持期(“L8细胞”)的蜕膜瘤,并在培养的第二天进行检测。17β-雌二醇(7×10⁻¹¹ M)和孕酮(6×10⁻⁸ M)显著抑制L5日取材细胞中PGE的积累:L8细胞培养物对雌二醇无明显反应,孕酮的作用明显减弱。孕酮刺激L5日取材细胞掺入[³H]胸腺嘧啶,但对L8细胞培养物无作用。其他前列腺素合成抑制剂,即皮质醇、氟芬那酸和吲哚美辛,对L5细胞的DNA合成也有刺激作用。PGE₂(5 - 10微克/毫升)抑制对照、吲哚美辛处理和孕酮处理的L5细胞培养物中的DNA合成,这表明孕酮诱导的DNA合成刺激可能部分归因于其对蜕膜细胞PGE积累的抑制作用。文中讨论了一种可能性,即在体内蜕膜发育的增殖期,DNA合成速率可能受类固醇诱导的组织中PGE含量变化的影响。