Tian X C, Berndtson A K, Fortune J E
Department of Physiology, Cornell University, Ithaca, New York 14853, USA.
Endocrinology. 1995 Nov;136(11):5102-10. doi: 10.1210/endo.136.11.7588247.
In cattle, a dramatic increase in plasma estradiol occurs during the short 2- to 3-day follicular phase. The objective of this study was to investigate the molecular mechanisms that mediate this critical change, specifically whether increases in the steroidogenic ability of granulosa and thecal cells of the preovulatory follicle are associated with increases in the levels of messenger RNA (mRNA) for steroidogenic enzymes. Luteolysis and a follicular phase were induced cycling Holstein heifers (n=15) by injection of a luteolytic dose of prostaglandin F2 alpha (PGF 2 alpha) on day 6 or 7 of the estrous cycle (day 0 = estrus), and preovulatory follicles were obtained at three stages of differentiation (0, 12, or 24 h post-PGF2 alpha treatment). To assess developmental changes in steroidogenesis in vivo, estradiol and androstenedione were measured in follicular fluid and in culture medium after a 3-h incubation of granulosa and thecal cells in defined medium with or without gonadotropins. To determine whether changes in mRNA for steroidogenic enzymes are associated with changes in follicular steroidogenesis, levels of mRNA for cytochrome P450 side-chain cleavage (P450scc), 3 beta-hydroxysteroid dehydrogenase (3 beta HSD), cytochrome P450 17 alpha-hydroxylase, and cytochrome P450 aromatase (P450arom) were measured in thecal and granulosa cells using ribonuclease protection assays. Concentrations of estradiol in follicular fluid were relatively high at time zero, increased significantly by 12 h, and increased further by 24 h post-PGF2 alpha treatment. However, the aromatizing activity of granulosa cells was high at the time of PGF2 alpha injection and did not increase significantly during the first 24 h after the initiation of luteolysis. The aromatizing activity of granulosa cells was reflected in levels of mRNA for P450arom, which was relatively abundant in granulosa cells obtained before luteolysis and did not increase further during the first 24 h of the follicular phase. Concentrations of androstenedione were virtually undetectable in follicular fluid at time zero and had increased dramatically by 12 and 24 h post-PGF2 alpha treatment. Similarly, thecal cells isolated at 24 h secreted 3-fold more androstenedione than cells isolated at the time of PGF2 alpha injection. Androstenedione production by thecal cells in response to LH was also markedly higher at 12 and 24 h than at the time of PGF2 alpha injection. Likewise; levels of mRNA for P450 17 alpha-hydroxylase increased significantly by 12 h post-PGF2 alpha treatment.(ABSTRACT TRUNCATED AT 400 WORDS)
在牛中,血浆雌二醇在短暂的2至3天卵泡期会急剧增加。本研究的目的是调查介导这一关键变化的分子机制,特别是排卵前卵泡颗粒细胞和膜细胞类固醇生成能力的增加是否与类固醇生成酶信使核糖核酸(mRNA)水平的增加相关。在发情周期的第6天或第7天(第0天=发情期),通过注射溶黄体剂量的前列腺素F2α(PGF2α)诱导处于发情周期的荷斯坦小母牛(n = 15)发生黄体溶解和卵泡期,并在分化的三个阶段(PGF2α处理后0、12或24小时)获取排卵前卵泡。为了评估体内类固醇生成的发育变化,在限定培养基中对颗粒细胞和膜细胞进行3小时孵育(添加或不添加促性腺激素)后,测量卵泡液和培养基中的雌二醇和雄烯二酮。为了确定类固醇生成酶mRNA的变化是否与卵泡类固醇生成的变化相关,使用核糖核酸酶保护试验测量膜细胞和颗粒细胞中细胞色素P450侧链裂解酶(P450scc)、3β-羟基类固醇脱氢酶(3βHSD)、细胞色素P450 17α-羟化酶和细胞色素P450芳香化酶(P450arom)的mRNA水平。PGF2α处理后0小时卵泡液中的雌二醇浓度相对较高,12小时时显著增加,24小时时进一步增加。然而,颗粒细胞的芳香化活性在注射PGF2α时较高,在黄体溶解开始后的最初24小时内没有显著增加。颗粒细胞的芳香化活性反映在P450arom的mRNA水平上,该mRNA在黄体溶解前获得的颗粒细胞中相对丰富,在卵泡期的最初24小时内没有进一步增加。0小时时卵泡液中几乎检测不到雄烯二酮的浓度,PGF2α处理后12小时和24小时显著增加。同样,在24小时分离的膜细胞分泌的雄烯二酮比在注射PGF2α时分离的细胞多3倍。膜细胞对促黄体生成素(LH)反应产生的雄烯二酮在12小时和24小时时也明显高于注射PGF2α时。同样,PGF2α处理后12小时,细胞色素P450 17α-羟化酶的mRNA水平显著增加。(摘要截短至400字)