Kubota T, Kamada S, Taguchi M, Aso T
Department of Obstetrics and Gynecology, Tokyo Medical and Dental University, Faculty of Medicine.
Nihon Sanka Fujinka Gakkai Zasshi. 1991 Nov;43(11):1515-20.
It has been reported that insulin-like growth factor (IGF) may play an important role in the feto-placental environment during pregnancy. The present study was undertaken to investigate the effect of IGF-I and IGF-II on prolactin (PRL) release from human decidual cells in vitro and in vivo. The human decidua in early pregnancy was obtained by D & C, and was enzymatically dispersed into a monocellular suspension. Monolayer cultures of these cells were exposed for 96 hours to either control media or medium supplemented with IGF-I and IGF-II. PRL levels in the media were measured by EIA. Five days after dispersion, the intracellular calcium concentration [( Ca]2+i) in cultured decidual cells was measured by the Fura-2 fluorescence method with a Spectrofluorometer. PRL and IGF-I levels in amniotic fluid of 2nd trimester and term pregnancy were measured by RIA for in vivo study. In an in vitro study, IGF-I increased PRL release from decidual cells significantly during a 96 hour culture. However, IGF-II did not enhance this PRL release. IGF-I stimulation had no effect on [Ca]2+i. In an in vivo study, amniotic fluid IGF-I levels in the 2nd trimester (139.8 +/- 28.1 ng/ml) were significantly higher than those in term pregnancy (46.4 +/- 14.2 ng/ml), and a significant positive correlation (r = 0.852, p less than 0.001) was observed between IGF-I and PRL levels in the amniotic fluid. The present in vivo and in vitro studies indicated that IGF-I plays an important role in PRL release from decidua into amniotic fluid.(ABSTRACT TRUNCATED AT 250 WORDS)
据报道,胰岛素样生长因子(IGF)在孕期胎儿 - 胎盘环境中可能发挥重要作用。本研究旨在探讨IGF - I和IGF - II在体外和体内对人蜕膜细胞催乳素(PRL)释放的影响。通过刮宫术获取早孕时的人蜕膜,并将其酶解分散成单细胞悬液。将这些细胞的单层培养物暴露于对照培养基或添加了IGF - I和IGF - II的培养基中96小时。通过酶免疫分析(EIA)测量培养基中的PRL水平。分散五天后,用荧光分光光度计通过Fura - 2荧光法测量培养的蜕膜细胞内的钙浓度[(Ca)2 + i]。通过放射免疫分析(RIA)测量孕中期和足月妊娠羊水的PRL和IGF - I水平以进行体内研究。在体外研究中,在96小时培养期间,IGF - I显著增加了蜕膜细胞的PRL释放。然而,IGF - II并未增强这种PRL释放。IGF - I刺激对[Ca]2 + i没有影响。在体内研究中,孕中期羊水IGF - I水平(139.8±28.1 ng/ml)显著高于足月妊娠(46.4±14.2 ng/ml),并且在羊水IGF - I和PRL水平之间观察到显著正相关(r = 0.852,p <0.001)。目前的体内和体外研究表明,IGF - I在蜕膜向羊水释放PRL中起重要作用。(摘要截断于250字)