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Inhibin removes the inhibitory effects of activin on steroid enzyme expression and androgen production by normal ovarian thecal cells

机译:抑制素消除了激活素对正常卵巢睾丸细胞的类固醇酶表达和雄激素产生的抑制作用

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摘要

Activin and inhibin are important local modulators of theca cell steroidogenesis in the ovary. Using a serum-free primary theca cell culture system, this study investigated the effects of inhibin on theca cell androgen production and expression of steroidogenic enzymes. Androstenedione secretion from theca cells cultured in media containing activin, inhibin and follistatin was assessed by RIA over 144 h. Activin (1-100 ng/ml) suppressed androstenedione production. Inhibin (1-100 ng/ml) blocked the suppressive effects of added activin, but increased androstenedione production when added alone, suggesting it was blocking endogenous activin produced by theca cells. Addition of SB-431542 (activin receptor inhibitor) and follistatin (500 ng/ml) increased androstenedione production, supporting this concept. Infection of theca cells with adenoviruses expressing inhibitory Smad6 or 7 increased androstenedione secretion, confirming that the suppressive effects of activin required activation of the Smad2/3 pathway. Activin decreased the expression levels of steroidogenic acute regulatory protein (STAR), whereas STAR expression was increased by inhibin and SB-431542, alone and in combination. CYP11A was unaffected. The expression of CYP17 encoding 17α-hydroxylase was unaffected by activin but increased by inhibin and SB-431542, and when added in combination the effect was further enhanced. The expression of 3β-hydroxysteroid dehydrogenase (3β-HSD) was significantly decreased by activin, while inhibin alone and in combination with SB-431542 both potently increased the expression of 3β-HSD. In conclusion, activin suppressed theca cell androstenedione production by decreasing the expression of STAR and 3β-HSD. Inhibin and other blockers of activin action reversed this effect, supporting the concept that endogenous thecal activin modulates androgen production in theca cells.
机译:激活素和抑制素是卵巢中卵泡膜细胞类固醇生成的重要局部调节剂。使用无血清原代theca细胞培养系统,本研究调查了抑制素对theca细胞雄激素产生和类固醇生成酶表达的影响。在144?h内用RIA评估了在含有激活素,抑制素和卵泡抑素的培养基中培养的theca细胞的雄烯二酮分泌。激活素(1-100μng/ ml)抑制雄烯二酮的产生。抑制素(1-100μng/ ml)阻断了添加的激活素的抑制作用,但是当单独添加时,其雄烯二酮的产量增加,表明它阻止了theca细胞产生的内源性激活素。 SB-431542(激活素受体抑制剂)和卵泡抑素(500μng/ ml)的加入增加了雄烯二酮的产生,支持了这一概念。表达抑制性Smad6或7的腺病毒感染theca细胞增加了雄烯二酮的分泌,这证实了激活素的抑制作用需要激活Smad2 / 3途径。激活素降低了类固醇生成的急性调节蛋白(STAR)的表达水平,而单独和组合使用抑制素和SB-431542可以提高STAR表达。 CYP11A不受影响。 CYP17编码的17α-羟化酶的表达不受激活素的影响,但受抑制素和SB-431542的影响而增加,并且当组合添加时,其作用进一步增强。激活素显着降低了3β-羟类固醇脱氢酶(3β-HSD)的表达,而单独的抑制素以及与SB-431542联合使用均抑制了3β-HSD的表达。总之,激活素通过降低STAR和3β-HSD的表达来抑制卵泡膜细胞雄烯二酮的产生。抑制素和激活素作用的其他阻滞剂逆转了这种作用,支持了内源性鞘内激活素调节卵泡膜细胞中雄激素产生的概念。

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    Young, J M; McNeilly, A S;

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  • 年度 2012
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  • 正文语种 eng
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