Karamouti M, Kollia P, Karligiotou E, Kallitsaris A, Prapas N, Kollios G, Seferiadis K, Vamvakopoulos N, Messinis I E
Department of Obstetrics and Gynaecology, Medical School, University of Thessalia, 22 Papakyriazi str. 412 22 Larissa, Greece.
J Mol Endocrinol. 2003 Aug;31(1):233-9. doi: 10.1677/jme.0.0310233.
Whether leptin is secreted by the human ovary is not known. The available data on leptin gene (ob gene) expression by human granulosa cells are conflicting. The aim of the present study was first to re-examine the expression of leptin messenger RNA (mRNA) by human granulosa cells and second to investigate if these cells have the ability to secrete leptin in cultures. Human luteinized granulosa cells were obtained from normal women undergoing in vitro fertilisation treatment after ovarian stimulation and follicle aspiration. The expression of ob gene was studied by Reverse-Transcriptase Polymerase Chain Reaction (RT-PCR) both in primary granulosa cells treated immediately after oocyte recovery and in cells cultured up to 24 h under baseline and hormonally stimulated conditions (FSH: 100 ng/ml, LH: 100 ng/ml). ob mRNA transcripts were not detected in luteinized granulosa cells, while they were present in adipose tIssue cDNA. Actin gene expression was detected in all studied samples. Using a sensitive radioimmunoassay (lower limit of detection 0.05 ng/ml), leptin was undetectable in the culture media at all points during the 72 h cultures, while at the same time significant amounts of oestradiol and progesterone were produced particularly after the addition of androstendione (1 microM) to the incubation media. These results demonstrate for the first time that leptin is not secreted by human luteinized granulosa cells in cultures. From a physiological point of view, this may contribute to the development of the optimal follicular environment for oocyte maturation during the preovulatory period.
目前尚不清楚人类卵巢是否分泌瘦素。关于人类颗粒细胞中瘦素基因(ob基因)表达的现有数据存在矛盾。本研究的目的一是重新检测人类颗粒细胞中瘦素信使核糖核酸(mRNA)的表达,二是研究这些细胞在培养中是否有分泌瘦素的能力。人类黄体化颗粒细胞取自接受卵巢刺激和卵泡抽吸后进行体外受精治疗的正常女性。通过逆转录聚合酶链反应(RT-PCR)研究ob基因在卵母细胞回收后立即处理的原代颗粒细胞以及在基线和激素刺激条件下(促卵泡激素:100纳克/毫升,促黄体生成素:100纳克/毫升)培养长达24小时的细胞中的表达。在黄体化颗粒细胞中未检测到ob mRNA转录本,而在脂肪组织cDNA中则有。在所有研究样本中均检测到肌动蛋白基因表达。使用灵敏的放射免疫分析法(检测下限为0.05纳克/毫升),在72小时培养期间的所有时间点,培养基中均未检测到瘦素,而与此同时,特别是在向孵育培养基中添加雄烯二酮(1微摩尔)后,产生了大量的雌二醇和孕酮。这些结果首次证明培养中的人类黄体化颗粒细胞不分泌瘦素。从生理学角度来看,这可能有助于在排卵前期为卵母细胞成熟形成最佳的卵泡环境。