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人绒毛膜促性腺激素对培养的人颗粒黄体细胞中雌二醇生成的刺激作用以及雄激素对促性腺激素刺激反应的拮抗作用。

Human chorionic gonadotropin stimulation of estradiol production and androgen antagonism of gonadotropin-stimulated responses in cultured human granulosa-luteal cells.

作者信息

Polan M L, Seu D, Tarlatzis B

出版信息

J Clin Endocrinol Metab. 1986 Apr;62(4):628-33. doi: 10.1210/jcem-62-4-628.

Abstract

Baseline and gonadotropin-stimulated estradiol production were examined in long term cultures of human granulosa-luteal cells isolated from women undergoing in vitro fertilization. Estradiol production declined by 70% during the first 48 h in culture and was minimally stimulated by the addition of hCG to the culture medium. During subsequent culture from 48-120 h estradiol production was significantly increased over control levels by hCG concentrations greater than 0.1 IU/ml. Incubation with testosterone stimulated estradiol production 100-fold in the presence and absence of gonadotropin. hCG (0.01-10 IU/ml) stimulated a 3- to 13-fold increase in progesterone production. However, at hCG concentrations greater than 1 IU/ml, coincubation with testosterone (10(-7) M) significantly inhibited progesterone production. Dihydrotestosterone also inhibited progesterone production, but to a lesser extent than testosterone. Freshly isolated granulosa-luteal cells specifically bound small amounts of [125I]hCG (less than 1,000 cpm/10(5) cells). Glycine buffer wash was shown to reversibly remove more than 88% of bound hCG and, in freshly isolated cells, increased [125I]hCG binding by 100%. In 5-day cultures, specific [125I] hCG binding nearly doubled from 52,000 cpm/10(5) cells in control cultures to 87,000 cpm/10(5) cells in cultures treated with hCG (0-5 IU/ml). At the highest concentration of hCG (5 IU/ml), testosterone (10(-7) M) significantly inhibited the amount of [125I]hCG specifically bound. In summary, estradiol production in long term cultures of granulosa-luteal cells appears to be gonadotropin dependent. In addition, the presence of testosterone (10(-7) M) antagonizes hCG-stimulated progesterone and LH receptor production by these cells.

摘要

在从接受体外受精的女性中分离出的人颗粒黄体细胞的长期培养中,检测了基础状态和促性腺激素刺激下的雌二醇生成情况。在培养的最初48小时内,雌二醇生成下降了70%,向培养基中添加人绒毛膜促性腺激素(hCG)对其刺激作用极小。在随后48至120小时的培养过程中,hCG浓度大于0.1 IU/ml时,雌二醇生成显著高于对照水平。在有或没有促性腺激素存在的情况下,与睾酮一起孵育可使雌二醇生成增加100倍。hCG(0.01 - 10 IU/ml)刺激孕酮生成增加3至13倍。然而,当hCG浓度大于1 IU/ml时,与睾酮(10⁻⁷ M)共同孵育会显著抑制孕酮生成。双氢睾酮也抑制孕酮生成,但程度小于睾酮。新鲜分离的颗粒黄体细胞特异性结合少量的[¹²⁵I]hCG(小于1000 cpm/10⁵细胞)。已证明用甘氨酸缓冲液洗涤可可逆地去除超过88%的结合hCG,并且在新鲜分离的细胞中,可使[¹²⁵I]hCG结合增加100%。在5天的培养中,特异性[¹²⁵I]hCG结合几乎翻倍,从对照培养中的52000 cpm/10⁵细胞增加到用hCG(0 - 5 IU/ml)处理的培养中的87000 cpm/10⁵细胞。在hCG的最高浓度(5 IU/ml)下,睾酮(10⁻⁷ M)显著抑制特异性结合的[¹²⁵I]hCG量。总之,颗粒黄体细胞长期培养中的雌二醇生成似乎依赖于促性腺激素。此外,睾酮(10⁻⁷ M)的存在会拮抗这些细胞中hCG刺激的孕酮和促黄体生成素(LH)受体生成。

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