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在缺乏蛋白质的情况下,雌二醇在体外抑制猪卵母细胞的减数分裂。

In the absence of protein, estradiol suppresses meiosis of porcine oocytes in vitro.

作者信息

Racowsky C, McGaughey R W

出版信息

J Exp Zool. 1982 Nov 20;224(1):103-10. doi: 10.1002/jez.1402240111.

Abstract

The effect of estradiol on the spontaneous maturation of porcine oocytes was investigated. Cumulus-enclosed (intact) and cumulus-free (denuded) oocytes were cultured in the presence of estradiol-17 beta (0 to 10 microgram/ml) in a chemically defined bicarbonate-buffered medium that contained either dextran or BSA, or in a complex Hepes-buffered medium that was supplemented with serum. After 24 hr, chromatin spreads were prepared and meiotic maturation was scored. The biochemical integrities of the cumulus cells were assessed by determination of the estradiol and progesterone content of spent media after culture of intact oocytes in the presence of 0.5 X 10(-6) M testosterone and 10 microgram/ml follicle-stimulating hormone. Estradiol did not significantly affect the onset of maturation of either intact or denuded oocytes that were cultured in medium containing either BSA or serum. In serum-supplemented medium, however, the progression of maturation beyond metaphase I was significantly affected by the steroid in a dose-dependent manner. The steroid significantly inhibited the release from meiotic arrest of both types of oocyte cultured in medium supplemented with dextran. Supplementation of all media with testosterone and FSH significantly stimulated the synthesis of estradiol by the cumulus cells, compared with that of control groups. The synthesis of progesterone, however, was significantly stimulated by testosterone and FSH only in the BSA and serum-supplemented media. It is concluded that exogenous estradiol has the capacity to arrest meiosis in vitro but that this capacity can only be expressed if no exogenous protein(s) is present. In the absence of exogenous protein, progesterone synthesis by the adherent cumulus cells is minimal.

摘要

研究了雌二醇对猪卵母细胞自发成熟的影响。将卵丘包裹(完整)和无卵丘(裸)的卵母细胞在含有17β-雌二醇(0至10微克/毫升)的情况下,培养于含有葡聚糖或牛血清白蛋白的化学限定碳酸氢盐缓冲培养基中,或培养于添加了血清的复合Hepes缓冲培养基中。24小时后,制备染色质铺展并对减数分裂成熟进行评分。在存在0.5×10⁻⁶ M睾酮和10微克/毫升促卵泡激素的情况下,将完整卵母细胞培养后,通过测定用过的培养基中的雌二醇和孕酮含量来评估卵丘细胞的生化完整性。雌二醇对培养于含有牛血清白蛋白或血清的培养基中的完整或裸卵母细胞的成熟起始没有显著影响。然而,在添加血清的培养基中,超过中期I的成熟进程受到该类固醇的显著影响,呈剂量依赖性。该类固醇显著抑制了培养于添加葡聚糖的培养基中的两种类型卵母细胞减数分裂阻滞的解除。与对照组相比,在所有培养基中添加睾酮和促卵泡激素显著刺激了卵丘细胞雌二醇的合成。然而,仅在添加牛血清白蛋白和血清的培养基中,睾酮和促卵泡激素显著刺激了孕酮的合成。得出的结论是,外源性雌二醇有能力在体外阻止减数分裂,但只有在不存在外源性蛋白质时这种能力才能表现出来。在没有外源性蛋白质的情况下,附着的卵丘细胞孕酮的合成极少。

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