Vanderhyden B C, Tonary A M
Department of Medicine, University of Ottawa Cancer Research Laboratories, Ontario, Canada.
Biol Reprod. 1995 Dec;53(6):1243-50. doi: 10.1095/biolreprod53.6.1243.
Mouse oocytes secrete a factor(s) that inhibits progesterone and enhances estradiol production by cumulus granulosa cells. The purpose of this study was to investigate the mechanisms by which the production of these steroids is modulated. Mouse oocyte-cumulus cell complexes (intact) and complexes from which the oocytes were removed microsurgically (oocytectomized; OOX) were cultured for up to 48 h in the presence of FSH (150 ng/ml) and testosterone (5 x 10(-7) M). For these experiments, all cells were obtained from antral follicles of 24- to 26-day-old mice primed with eCG. Intact complexes produced primarily estradiol, with significant accumulation occurring between 24 and 48 h. In contrast, OOX complexes produced little estradiol but, starting at 18 h of culture, released significantly more progesterone than did intact complexes. Progesterone accumulation in cocultures of denuded oocytes with either OOX complexes or monolayers of mural granulosa cells was significantly reduced compared to that with OOX complexes or mural granulosa cells cultured alone. If dibutyryl cAMP replaced FSH in the cocultures, similar results were obtained, suggesting that the oocyte-secreted steroid-regulating factor acts downstream of the generation of cAMP to inhibit progesterone production. Since estradiol can inhibit progesterone production by granulosa cells, we investigated the possibility that the increased progesterone released by OOX complexes was secondary to the lower estradiol production. Intact complexes cultured in the presence of the nonaromatizable androgen, 5 alpha-dihydrotestosterone, or steroidal (4-hydroxyandrostenedione) or non-steroidal (CGS 16949A) aromatase inhibitors produced little estradiol; however, progesterone production by these complexes was no different from that of estradiol-producing intact complexes. These results suggest that the steroid-regulating factor(s) secreted by occytes acts to regulate granulosa cell production of estradiol and progesterone by independent mechanisms.
小鼠卵母细胞分泌一种因子,该因子可抑制孕酮,并增强卵丘颗粒细胞产生雌二醇。本研究的目的是探究调节这些类固醇产生的机制。将小鼠卵母细胞-卵丘细胞复合体(完整的)以及通过显微手术去除卵母细胞后的复合体(去卵母细胞;OOX)在促卵泡激素(FSH,150 ng/ml)和睾酮(5×10⁻⁷ M)存在的情况下培养长达48小时。对于这些实验,所有细胞均取自用孕马血清促性腺激素(eCG)预处理的24至26日龄小鼠的窦状卵泡。完整的复合体主要产生雌二醇,在24至48小时之间有显著积累。相比之下,OOX复合体产生的雌二醇很少,但从培养18小时开始,释放的孕酮比完整复合体显著更多。与单独培养的OOX复合体或壁层颗粒细胞单层相比,裸卵与OOX复合体或壁层颗粒细胞单层共培养时孕酮的积累显著减少。如果在共培养中用二丁酰环磷腺苷(dibutyryl cAMP)替代FSH,会得到相似的结果,这表明卵母细胞分泌的类固醇调节因子在环磷腺苷(cAMP)生成的下游起作用以抑制孕酮的产生。由于雌二醇可抑制颗粒细胞产生孕酮,我们研究了OOX复合体释放的孕酮增加是否继发于雌二醇产生降低的可能性。在不可芳香化的雄激素5α-二氢睾酮、甾体类(4-羟基雄烯二酮)或非甾体类(CGS 16949A)芳香化酶抑制剂存在的情况下培养的完整复合体产生的雌二醇很少;然而,这些复合体产生的孕酮与产生雌二醇的完整复合体没有差异。这些结果表明,卵母细胞分泌的类固醇调节因子通过独立的机制调节颗粒细胞产生雌二醇和孕酮。