Harlow C R, Shaw H J, Hillier S G, Hodges J K
Institute of Obstetrics and Gynaecology, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.
Endocrinology. 1988 Jun;122(6):2780-7. doi: 10.1210/endo-122-6-2780.
Preovulatory changes in the steroidogenic function of primate granulosa cells were studied using the cyclic marmoset (Callithrix jacchus) as a model. Antral follicles (greater than or equal to 0.5 mm diameter) were dissected from mid-late follicular phase ovaries (7 days after prostaglandin-induced luteolysis) and classified by diameter as small (0.5-1.0 mm), medium (1.1-1.9 mm) or large (greater than or equal to 2.0 mm). Granulosa cells from follicles in each size category were isolated and pooled to assess steroid biosynthesis. The aromatase activity of freshly isolated granulosa cells from large follicles was 200 times greater than that of small follicles, confirming their relatively advanced preovulatory status. Granulosa cells were cultured for 48 h in the presence and absence of human (h) FSH (0.1 ng/ml), with and without 0.1 microM androgen (testosterone or 5 alpha-dihydrotestosterone), to assess basal and hormone-responsive steroidogenesis (progesterone accumulation in culture medium and aromatase activity in washed granulosa cell monolayers). Basal granulosa cell steroidogenesis increased with follicular size, and there was a development-related pattern of response to hFSH and androgen. hFSH responsiveness (maximum fold-stimulation induced by hFSH) declined with follicular size, being 2-6 times greater for granulosa cells from small vs. large follicles. On the other hand, hFSH sensitivity increased with follicular size; the dose of hFSH giving 50% of the maximum response (ED50) for cells from large follicles being 10-20 times less than that of cells from small follicles. For granulosa cells from small follicles, treatment with 0.1 microM androgen in the presence of hFSH led to dramatic (up to 16-fold) enhancement of steroidogenic responses to hFSH. In contrast, for granulosa cells from large follicles, the presence of androgen substantially inhibited aromatase activity stimulated by hFSH and had weak inhibitory effects on progesterone accumulation. These results show that granulosa cell steroidogenesis becomes increasingly sensitive to hFSH during preovulatory follicular development in marmosets. The marked ability of androgen to directly augment hFSH-responsive steroidogenesis in vitro is lost during preovulatory development, such that androgen acts in mature granulosa cells to suppress hFSH-stimulated aromatase activity. These observations are evidence of development-dependent changes in granulosa cell responses to FSH and androgens which may contribute to the control of preovulatory follicular development in primates.
以性周期中的狨猴(Callithrix jacchus)为模型,研究了灵长类动物颗粒细胞类固醇生成功能的排卵前变化。从卵泡期中期至后期(前列腺素诱导黄体溶解7天后)的卵巢中解剖出直径大于或等于0.5mm的窦状卵泡,并按直径分为小卵泡(0.5 - 1.0mm)、中卵泡(1.1 - 1.9mm)或大卵泡(大于或等于2.0mm)。分离并汇集每个大小类别卵泡中的颗粒细胞,以评估类固醇生物合成。新鲜分离的大卵泡颗粒细胞的芳香化酶活性比小卵泡高200倍,证实了它们相对较先进的排卵前状态。将颗粒细胞在有和无人类(h)FSH(0.1ng/ml)、有和无0.1μM雄激素(睾酮或5α - 双氢睾酮)的情况下培养48小时,以评估基础和激素反应性类固醇生成(培养基中孕酮积累和洗涤后的颗粒细胞单层中的芳香化酶活性)。基础颗粒细胞类固醇生成随卵泡大小增加,并且对hFSH和雄激素的反应存在与发育相关的模式。hFSH反应性(hFSH诱导的最大刺激倍数)随卵泡大小下降,小卵泡颗粒细胞的反应性比大卵泡颗粒细胞大2 - 6倍。另一方面,hFSH敏感性随卵泡大小增加;使大卵泡细胞产生最大反应50%(ED50)的hFSH剂量比小卵泡细胞低10 - 20倍。对于小卵泡颗粒细胞,在hFSH存在下用0.1μM雄激素处理导致对hFSH的类固醇生成反应显著增强(高达16倍)。相反,对于大卵泡颗粒细胞,雄激素的存在显著抑制hFSH刺激的芳香化酶活性,并对孕酮积累有微弱的抑制作用。这些结果表明,在狨猴排卵前卵泡发育过程中,颗粒细胞类固醇生成对hFSH变得越来越敏感。在排卵前发育过程中,雄激素在体外直接增强hFSH反应性类固醇生成的显著能力丧失,使得雄激素在成熟颗粒细胞中抑制hFSH刺激的芳香化酶活性。这些观察结果证明了颗粒细胞对FSH和雄激素的反应存在发育依赖性变化,这可能有助于控制灵长类动物排卵前卵泡的发育。