Nemme R, Acker G M, Papiernik E
INSERM Unité 187, Clamart, France.
Eur J Obstet Gynecol Reprod Biol. 1988 Jul;28(3):221-8. doi: 10.1016/0028-2243(88)90032-9.
Cultured monolayers of endometrial cells synthesized PGE2, PGF2 alpha, 13,14-dihydro-15-keto-PGF2 alpha (DHKF2 alpha), TXB2 and 6-keto-PGF1 alpha. Synthesis increased with the duration of culture, reaching a maximum at approximately the 20th day for PGF2 alpha and PGE2; PGF2 alpha levels always exceeded those of PGE2. Transformation of PGF2 alpha into DHKF2 alpha was minimal. Maximal levels of TXB2 and 6-keto-PGF1 alpha were noted after 7 and 14 days respectively. After three weeks, traces of DHKF2 alpha, TXB2 and 6-keto-PGF1 alpha were noted, whereas PGF2 alpha levels were marked after 30 days of culture. Addition of progesterone (0.32 ng/ml) reduced PG production, notably for PGF2 alpha, but promoted prolactin synthesis, indicating that this progesterone concentration induced decidualization of endometrial cells during the first days of culture.
培养的单层子宫内膜细胞能合成前列腺素E2(PGE2)、前列腺素F2α(PGF2α)、13,14-二氢-15-酮-前列腺素F2α(DHKF2α)、血栓素B2(TXB2)和6-酮-前列腺素F1α(6-keto-PGF1α)。合成量随培养时间增加,PGF2α和PGE2在大约第20天达到最大值;PGF2α水平始终超过PGE2。PGF2α向DHKF2α的转化极少。TXB2和6-keto-PGF1α的最高水平分别在7天和14天后出现。三周后,仅检测到微量的DHKF2α、TXB2和6-keto-PGF1α,而培养30天后PGF2α水平显著升高。添加孕酮(0.32 ng/ml)可降低PG生成,尤其是PGF2α,但促进催乳素合成,表明该孕酮浓度在培养初期诱导了子宫内膜细胞蜕膜化。