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子宫基质增强小鼠子宫上皮细胞对雌二醇的反应。

Augmentation of the response of mouse uterine epithelial cells to estradiol by uterine stroma.

作者信息

Inaba T, Wiest W G, Strickler R C, Mori J

机构信息

Department of Obstetrics and Gynecology, Washington University School of Medicine, St. Louis, Missouri.

出版信息

Endocrinology. 1988 Sep;123(3):1253-8. doi: 10.1210/endo-123-3-1253.

Abstract

The effect of estrogen on the in vitro growth of mouse uterine epithelial cells was assessed. Epithelial cells from the immature mouse uterus were successfully cultivated in a 1:1 mixture of Dulbecco's Modified Eagle's Medium and Ham's F-12 supplemented with insulin (5 micrograms/ml), transferrin (10 micrograms/ml), hydrocortisone (10(-7) M), BSA (2 mg/ml), and fetuin (1 mg/ml). Addition of 17 beta-estradiol in the range of 1-100 nM did not significantly change the total DNA content of the epithelial cells. A binding component of [3H]estradiol by cultured uterine cells was shown to be specific, saturable, and of high affinity. Kd values for specific binding by epithelial and stromal cells were 1.0-1.7 x 10(-10) M. Maximal specific binding was 0.74 and 2.3 fmol/micrograms DNA for epithelial and stromal cells, respectively. Treatment of epithelial and stromal cells for 4 days with 10 nM estradiol led to a 2- to 6-fold increase in progesterone receptor concentration. Treatment of epithelial and stromal cells in mixed culture for 4 days with 10 nM estradiol resulted in a significant increase in total DNA. That epithelial-stromal contact was critical for estradiol stimulation was shown by the fact that if the cell types were separated into two compartments which still allowed free media mixing, total DNA was not enhanced by estradiol. These observations are organized into a model for mitogenic action of estradiol that seems to reconcile observed disparities in the action of the hormone in vivo and in vitro.

摘要

评估了雌激素对小鼠子宫上皮细胞体外生长的影响。将未成熟小鼠子宫的上皮细胞成功培养于含有胰岛素(5微克/毫升)、转铁蛋白(10微克/毫升)、氢化可的松(10⁻⁷摩尔)、牛血清白蛋白(2毫克/毫升)和胎球蛋白(1毫克/毫升)的杜氏改良伊格尔培养基与哈姆氏F-12的1:1混合培养基中。添加1-100纳摩尔范围内的17β-雌二醇并未显著改变上皮细胞的总DNA含量。培养的子宫细胞对[³H]雌二醇的结合成分显示具有特异性、可饱和性且亲和力高。上皮细胞和基质细胞特异性结合的解离常数(Kd)值为1.0-1.7×10⁻¹⁰摩尔。上皮细胞和基质细胞的最大特异性结合分别为0.74和2.3飞摩尔/微克DNA。用10纳摩尔雌二醇处理上皮细胞和基质细胞4天导致孕酮受体浓度增加2至6倍。用10纳摩尔雌二醇处理混合培养的上皮细胞和基质细胞4天导致总DNA显著增加。如果将细胞类型分隔在两个仍允许培养基自由混合的隔室中,雌二醇不会增强总DNA,这一事实表明上皮-基质接触对雌二醇刺激至关重要。这些观察结果被整理成一个雌激素促有丝分裂作用的模型,该模型似乎调和了体内和体外观察到的激素作用差异。

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