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未成熟猪睾丸间质细胞原代培养中的雄激素生成

Androgen production in primary culture of immature porcine Leydig cells.

作者信息

Haour F, Bommelaer M C, Bernier M, Sanchez P, Saez J, Mather J P

出版信息

Mol Cell Endocrinol. 1983 Apr;30(1):73-84. doi: 10.1016/0303-7207(83)90202-2.

Abstract

The present paper examines the steroidogenic responsiveness of immature porcine Leydig cells in primary culture. Both testosterone (T) and dehydroepiandrosterone sulfate (DHAS) secretion were measured under basal conditions and after stimulation with human chorionic gonadotropin (hCG) (25 ng/ml). In medium supplemented with insulin, transferrin, epidermal growth factor (3H) and 0.1% calf serum, cells survived 3-5 days in culture. The production of steroids (under hCG stimulation) is poor on day 0-1 of the culture. On day 2-4 basal T and DHAS levels are 1.9 and 17.0 ng/10(6) cells/24 h. The addition of hCG stimulated T and DHAS production 19- and 6-fold respectively and the average productions were 37 and 109 ng/10(6) cells/24 h. Increasing the serum to 0.5% did not change the viability of the cultures, but increased hCG stimulated T and DHAS production (183 and 188 ng/10(6) cells/24 h). The addition of alpha-tocopherol (vitamin E) to 0.1% calf serum led to a 4-fold increase in stimulated T production (142 ng/10(6) cells/24 h) and maintained full cell viability for more than 5 days. Measurement of 3 beta-ol steroid dehydrogenase activity indicates that the amount of enzyme is 4 times higher at day 2 than at day 0 and 1 (with or without hCG), suggesting a spontaneous maturation of the cells in culture. This might explain the increased T production with time in culture. In cumulative experiments (24 h) the cells do not seem to be desensitized to hCG stimulation following prolonged exposure to 25 ng hCG since the daily steroid production is increasing with time in culture. However, kinetic studies show that steroidogenesis is not linear over a 24 h period. In cumulative experiments the steroid production stops between 12 and 16 h following hCG exposure (5 and 100 ng/ml) and resumes following a medium change. These results suggest that some inhibitory compounds are accumulated in the medium and are controlling the Leydig cell function. Moreover high doses of hCG (100 ng/ml) result in a lower production of steroids and an earlier plateau in the case of DHAS. These results demonstrate that porcine Leydig cells can live and differentiate in hormone- and vitamin-supplemented medium and that auto-feedback mechanisms inhibiting steroid accumulation take place under in vitro conditions.

摘要

本文研究了原代培养的未成熟猪睾丸间质细胞的类固醇生成反应性。在基础条件下以及用人绒毛膜促性腺激素(hCG,25 ng/ml)刺激后,分别测定了睾酮(T)和硫酸脱氢表雄酮(DHAS)的分泌情况。在添加了胰岛素、转铁蛋白、表皮生长因子(3H)和0.1%小牛血清的培养基中,细胞在培养中存活3 - 5天。在培养的第0 - 1天,(在hCG刺激下)类固醇的产生较少。在第2 - 4天,基础T和DHAS水平分别为1.9和17.0 ng/10⁶细胞/24小时。添加hCG分别刺激T和DHAS的产生增加了19倍和6倍,平均产量分别为37和109 ng/10⁶细胞/24小时。将血清增加到0.5%并没有改变培养物的活力,但增加了hCG刺激的T和DHAS的产生(183和188 ng/10⁶细胞/24小时)。向0.1%小牛血清中添加α-生育酚(维生素E)导致刺激后的T产量增加了4倍(142 ng/10⁶细胞/24小时),并使细胞在5天以上保持完全活力。3β-醇类固醇脱氢酶活性的测定表明,在第2天该酶的量比第0天和第1天(无论有无hCG)高4倍,这表明培养中的细胞发生了自发成熟。这可能解释了培养过程中T产量随时间增加的现象。在累积实验(24小时)中,长时间暴露于25 ng hCG后,细胞似乎并未对hCG刺激产生脱敏,因为培养过程中每日类固醇产量随时间增加。然而,动力学研究表明,类固醇生成在24小时内不是线性的。在累积实验中,hCG暴露(5和100 ng/ml)后12至16小时类固醇产生停止,换液后恢复。这些结果表明,培养基中积累了一些抑制性化合物并控制着睾丸间质细胞的功能。此外,高剂量的hCG(100 ng/ml)导致类固醇产生降低,对于DHAS则导致更早达到平台期。这些结果表明,猪睾丸间质细胞可以在补充了激素和维生素的培养基中存活并分化,并且在体外条件下会发生抑制类固醇积累的自身反馈机制。

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