Grossman Michael P, Nakajima Steven T, Fallat Mary E, Siow Yong
Department of Obstetrics and Gynecology, University of Louisville, Louisville, Kentucky 40292, USA.
Fertil Steril. 2008 May;89(5 Suppl):1364-70. doi: 10.1016/j.fertnstert.2007.03.066. Epub 2007 May 22.
To investigate the effects of Müllerian-inhibiting substance (MIS) on cytochrome P450 aromatase (CYP19) gene expression in cultured human granulosa lutein cells (GLC).
In vitro primary cell culture study.
Academic research laboratory and hospital-based fertility center.
PATIENT(S): Eight normo-ovulatory patients undergoing IVF procedures due to male factor or tubal infertility.
INTERVENTION(S): Serum and follicular fluid (FF) collected and stored at -80 degrees C until assayed. Granulosa lutein cells were harvested from follicular aspirates obtained during oocyte retrieval and cultured for 7 days with media in the presence or absence of MIS (10 ng/mL) or FSH 0.2 IU/mL.
MAIN OUTCOME MEASURE(S): Serum and FF levels of E2 and MIS, and E2 production by GLC in culture. Levels of CYP19 mRNA in cultured GLC were determined by quantitative polymerase chain reaction (PCR) and CYP19 protein by Western blot. Statistical comparison used ANOVA and post hoc Tukey tests.
RESULT(S): Follicle-stimulating hormone significantly increased E2 production in cultured GLC compared with control. The increase in E2 production is associated with higher levels of CYP19 mRNA and protein in GLC. The presence of MIS significantly inhibited FSH-induced E2 production, with concomitant reduction in CYP19mRNA and protein levels.
CONCLUSION(S): Müllerian-inhibiting substance inhibits FSH augmentation of CYP19 enzyme activity and CYP19 gene expression in GLC. These findings may help to explain the association of high MIS levels and low FF E2 levels reported in women with polycystic ovary syndrome (PCOS).
研究苗勒管抑制物质(MIS)对培养的人颗粒黄体细胞(GLC)中细胞色素P450芳香化酶(CYP19)基因表达的影响。
体外原代细胞培养研究。
学术研究实验室和医院附属的生育中心。
8名因男性因素或输卵管性不孕而接受体外受精程序的排卵正常患者。
收集血清和卵泡液(FF)并储存在-80℃直至检测。从取卵时获得的卵泡抽吸物中收获颗粒黄体细胞,在有或无MIS(10 ng/mL)或FSH 0.2 IU/mL的情况下用培养基培养7天。
血清和FF中E2和MIS的水平,以及培养的GLC产生的E2。通过定量聚合酶链反应(PCR)测定培养的GLC中CYP19 mRNA的水平,通过蛋白质印迹法测定CYP19蛋白。统计比较采用方差分析和事后Tukey检验。
与对照组相比,促卵泡激素显著增加了培养的GLC中E2的产生。E2产生的增加与GLC中较高水平的CYP19 mRNA和蛋白相关。MIS的存在显著抑制了FSH诱导的E2产生,同时CYP19 mRNA和蛋白水平降低。
苗勒管抑制物质抑制FSH增强GLC中CYP19酶活性和CYP19基因表达。这些发现可能有助于解释多囊卵巢综合征(PCOS)女性中报道的高MIS水平和低FF E2水平之间的关联。