Veldhuis J D, Klase P A, Strauss J F, Hammond J M
Endocrinology. 1982 Aug;111(2):441-7. doi: 10.1210/endo-111-2-441.
Well differentiated swine granulosa cells in monolayer culture were employed to investigate the mechanisms by which estradiol amplifies the stimulatory actions of LH in the later stages of follicular maturation. The facilitative interaction between estradiol and LH could not be attributed to altered rates of catabolism of progesterone to 20 alpha-hydroxypregn-4-en-3-one. Moreover, estradiol, LH, and estradiol combined with LH clearly stimulated pregnenolone production, measured in the presence of trilostane, to inhibit 3 beta-hydroxysteroid dehydrogenase-delta-5-4-isomerase activity. Thus, at least one component of the synergism between estradiol and LH must reside at or proximal to the cholesterol side-chain cleavage system. In the absence of lipoproteins, the magnitude of the synergism between estradiol and LH was significantly reduced. However, the facilitative interaction between estradiol and LH could still be observed in lipoprotein-deficient and serum-free medium and after the administration of ML-236B to suppress the de novo biosynthesis of cholesterol. In contrast, estradiol alone and LH alone significantly augmented progesterone production in the presence of the oxygenated sterol 5-cholesten-3 beta,25-diol, which can serve as an effective substrate for cholesterol side-chain cleavage. In addition, in the presence of 5-cholesten-3 beta,25-diol, the magnitude of the synergism between estradiol and LH was increased markedly. Thus, the present studies demonstrate that estradiol and LH significantly stimulate progesterone production, at least in part, by augmenting pregnenolone biosynthesis, but not by inhibiting progesterone catabolism. Studies with 5-cholesten-3 beta-25-diol further suggest that estradiol and LH increase cholesterol side-chain cleavage activity. These observations delineate important mechanisms by which estradiol and LH prepare well differentiated granulosa cells for the high rates of steroidogenesis that are ultimately required in the corpus luteum.
采用单层培养的高分化猪颗粒细胞来研究雌二醇在卵泡成熟后期增强促黄体生成素(LH)刺激作用的机制。雌二醇与LH之间的促进性相互作用不能归因于孕酮向20α-羟基孕-4-烯-3-酮的分解代谢速率改变。此外,雌二醇、LH以及雌二醇与LH联合使用均能在曲洛司坦存在的情况下明显刺激孕烯醇酮生成,以抑制3β-羟基类固醇脱氢酶-δ5-4-异构酶活性。因此,雌二醇与LH协同作用的至少一个组分必定存在于胆固醇侧链裂解系统或其近端。在无脂蛋白的情况下,雌二醇与LH之间协同作用的强度显著降低。然而,在缺乏脂蛋白和无血清的培养基中,以及在给予ML-236B以抑制胆固醇从头生物合成后,仍可观察到雌二醇与LH之间的促进性相互作用。相反,在含氧固醇5-胆甾烯-3β,25-二醇存在的情况下,单独的雌二醇和单独的LH均能显著增加孕酮生成,5-胆甾烯-3β,25-二醇可作为胆固醇侧链裂解的有效底物。此外,在5-胆甾烯-3β,25-二醇存在的情况下,雌二醇与LH之间协同作用的强度明显增加。因此,本研究表明,雌二醇和LH至少部分地通过增强孕烯醇酮生物合成而非抑制孕酮分解代谢来显著刺激孕酮生成。对5-胆甾烯-3β-25-二醇的研究进一步表明,雌二醇和LH可增加胆固醇侧链裂解活性。这些观察结果阐明了雌二醇和LH使高分化颗粒细胞为黄体最终所需的高类固醇生成速率做好准备的重要机制。