首页> 外文期刊>Peptides: An International Journal >Effects of kisspeptin-10 on progesterone secretion in cultured chicken ovarian granulosa cells from preovulatory (F1-F3) follicles.
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Effects of kisspeptin-10 on progesterone secretion in cultured chicken ovarian granulosa cells from preovulatory (F1-F3) follicles.

机译:Kisspeptin-10对排卵前(F1-F3)卵泡培养的鸡卵巢颗粒细胞中孕酮分泌的影响。

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The effect of kisspeptin-10 (Kp-10) on the secretion of progesterone (P(4)) was investigated in cultured granulosa cells from F(1) to F(3) follicles of hens. The results showed that granulosa cells were stained with clear signals for kisspeptin using immunocytochemistry with the specific antibody against Kp-10. Among 10, 100 and 1000 nM concentrations tested, 100 nM Kp-10 treated for 24h significantly increased P(4) secretion in granulosa cells from F(1) to F(3) follicles. After 24h and 48 h of treatment, 100 nM Kp-10 showed a significant increase in P(4) secretion, while after 72 h of treatment P(4) secretion was markedly decreased by Kp-10 compared to the control group (P<0.05). F(1) and F(2/3) cells treated with 100 nM Kp-10 for 24h showed significantly increased viability (P<0.05) and which was in parallel to a marked increase in P(4) secretion (P<0.01). Real-time PCR results showed that the gene expression of the steroidogenic acute regulatory protein (StAR), cytochrome P450 side-chain cleavage (P450scc) and the enzyme 3beta-hydroxysteroid dehydrogenase (3beta-HSD) in F(1) and F(2/3) granulosa cells was significantly up-regulated by 24h-100 nM Kp-10 treatment (P<0.05 versus P<0.01, respectively). However, there was no significant difference in StAR, P450scc and 3beta-HSD protein content between control and the Kp-10 treated group (P>0.05). These results indicate that Kp-10 stimulates P(4) secretion in cultured chicken granulosa cells, which was associated with an up-regulation in StAR, P450scc and 3beta-HSD gene transcription.
机译:在从母鸡F(1)到F(3)卵泡培养的颗粒细胞中研究了Kisspeptin-10(Kp-10)对孕酮(P(4))分泌的影响。结果显示,使用针对Kp-10的特异性抗体的免疫细胞化学技术,颗粒细胞被kipseptin的信号清楚地染色。在测试的10、100和1000 nM浓度中,处理24小时的100 nM Kp-10显着增加了颗粒细胞从F(1)到F(3)卵泡的P(4)分泌。治疗24小时和48小时后,与对照组相比,100 nM Kp-10显示P(4)分泌显着增加,而治疗72小时后Kp-10显着降低P(4)分泌(P < 0.05)。用100 nM Kp-10处理24小时的F(1)和F(2/3)细胞显示出显着提高的生存力(P <0.05),并且与P(4)分泌的显着增加平行(P <0.01) 。实时PCR结果表明,类固醇生成的急性调节蛋白(StAR),细胞色素P450侧链裂解(P450scc)和3β-羟基类固醇脱氢酶(3beta-HSD)在F(1)和F(2)中的基因表达/ 3)通过24h-100 nM Kp-10处理,颗粒细胞明显上调(分别为P <0.05与P <0.01)。然而,对照组和Kp-10治疗组之间的StAR,P450scc和3beta-HSD蛋白含量没有显着差异(P> 0.05)。这些结果表明,Kp-10刺激培养的鸡颗粒细胞分泌P(4),这与StAR,P450scc和3beta-HSD基因转录的上调相关。

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