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缺氧促进牛颗粒细胞黄体化过程中的孕酮合成。

Hypoxia promotes progesterone synthesis during luteinization in bovine granulosa cells.

作者信息

Yoshioka Shin, Nishimura Ryo, Okuda Kiyoshi

机构信息

Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama 700-8530, Japan.

出版信息

J Reprod Dev. 2014;60(3):194-201. doi: 10.1262/jrd.2014-014. Epub 2014 Mar 1.

Abstract

To determine whether hypoxia has an effect on luteinization, we examined the influence of hypoxia on a model of bovine luteinizing and non-luteinizing granulosa cell culture. The granulosa cells were obtained from small antral follicles (≤ 6 mm in diameter). To induce luteinization, the cells were treated for 24 h with insulin (2 µg/ml), forskolin (10 µM) or insulin in combination with forskolin at 20% O2. After 24 h, progesterone (P4) production was higher in the treated cells, which we defined as luteinizing granulosa cells, than in non-treated cells, which we defined as non-luteinizing granulosa cells. P4 production by non-luteinizing granulosa cells was not affected by hypoxia (24 h at 10% and 5% O2), while P4 production by granulosa cells treated with insulin in combination with forskolin was significantly increased under hypoxia (24 h at 10% and 5% O2). Because hypoxia affected P4 production by the luteinizing granulosa cells but not by the non-luteinizing granulosa cells, hypoxia seems to promote P4 production during, rather than before, luteinization. In the cells treated with insulin in combination with forskolin, mRNA and protein expression of steroidogenic acute regulatory protein (StAR) and protein expression of 3β-hydroxysteroid dehydrogenase (3β-HSD) increased under 10% O2, while mRNA and protein expressions of key protein and enzymes in P4 biosynthesis did not increase under 5% O2. The overall results suggest that hypoxia plays a role in progressing and completing the luteinization by enhancing P4 production through StAR as well as 3β-HSD expressions in the early time of establishing the corpus luteum.

摘要

为了确定缺氧是否对黄体化有影响,我们研究了缺氧对牛黄体化和非黄体化颗粒细胞培养模型的影响。颗粒细胞取自小卵泡(直径≤6mm)。为诱导黄体化,细胞在20%氧气条件下用胰岛素(2µg/ml)、福司可林(10µM)或胰岛素与福司可林联合处理24小时。24小时后,经处理的细胞(我们定义为黄体化颗粒细胞)中的孕酮(P4)产量高于未处理的细胞(我们定义为非黄体化颗粒细胞)。非黄体化颗粒细胞的P4产量不受缺氧(10%和5%氧气条件下24小时)的影响,而胰岛素与福司可林联合处理的颗粒细胞在缺氧条件下(10%和5%氧气条件下24小时)P4产量显著增加。由于缺氧影响黄体化颗粒细胞的P4产量,但不影响非黄体化颗粒细胞的P4产量,缺氧似乎在黄体化过程中而非黄体化之前促进P4的产生。在胰岛素与福司可林联合处理的细胞中,在10%氧气条件下,类固醇生成急性调节蛋白(StAR)的mRNA和蛋白表达以及3β-羟基类固醇脱氢酶(3β-HSD)的蛋白表达增加,而在5%氧气条件下,P4生物合成中关键蛋白和酶的mRNA和蛋白表达没有增加。总体结果表明,缺氧通过在黄体形成早期增强StAR以及3β-HSD的表达来提高P4产量,从而在黄体化的进展和完成过程中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c4/4085383/a21e292eb6cc/jrd-60-194-g001.jpg

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