首页> 外文期刊>The Journal of Reproduction and Development >Effects of gonadotropin-releasing hormone agonist on human chorionic gonadotropin activity in granulosa cells of immature female rats
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Effects of gonadotropin-releasing hormone agonist on human chorionic gonadotropin activity in granulosa cells of immature female rats

机译:促性腺激素释放激素激动剂对未成熟雌性大鼠颗粒细胞绒毛膜促性腺激素活性的影响

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Although the expression of gonadotropin-releasing hormone (GnRH) in the ovaries is well established, its physiological role remains unknown. The aim of this study was to determine whether ovarian GnRH mediates the actions of human chorionic gonadotropin (hCG) in the granulosa cells of immature female rats. Follicular growth was induced by administration of pregnant mare serum gonadotropin (PMSG, 15 IU/0.15 ml) on day 25 after birth, and hCG (20 IU/0.2 ml) was administered on day 27 revealing the increase of plasma progesterone level. Primary cultures of granulosa cells were established from large follicles 2 days after PMSG treatment. Progesterone synthesis was augmented by hCG in a dose-dependent manner. Annexin A5 (ANXA5), a biomarker of GnRH, was expressed in the granulosa-luteal cells after hCG treatment, as shown by immunohistochemistry, suggesting that hCG treatment induced GnRH action. The GnRH mRNA level was increased by hCG, and treatment with GnRH agonist (GnRHa) increased ANXA5 mRNA levels in the primary cultures of granulosa cells. Concomitant incubation of GnRH (10–7 M) or GnRHa (fertirelin acetate, 10–8 M) with hCG suppressed progesterone synthesis during a 3 h incubation period. The mRNA expression of luteinizing hormone receptor (LHR) and follicle-stimulating hormone receptor (FSHR) was synergistically stimulated and suppressed by hCG and GnRHa, respectively. GnRHa stimulated p21 expression, and GnRHa and hCG synergistically reduced the mRNA expression levels of p27 and FOXO1. These data suggest that GnRH induced by LH may have a role for the LH-mediated luteinization of granulosa cells. In addition, ANXA5 may be involved in GnRH action. GnRH-ANXA5 would be an important mechanism in cell differentiation.
机译:尽管促性腺激素释放激素(GnRH)在卵巢中的表达已被很好地确定,但其生理作用仍然未知。这项研究的目的是确定卵巢GnRH是否介导未成熟雌性大鼠颗粒细胞中绒毛膜促性腺激素(hCG)的作用。出生后第25天通过给予母马血清促性腺激素(PMSG,15 IU / 0.15 ml)诱导卵泡生长,第27天给予hCG(20 IU / 0.2 ml),这表明血浆孕酮水平升高。 PMSG处理2天后,从大卵泡建立颗粒细胞的原代培养。 hCG以剂量依赖的方式增强了孕酮的合成。免疫组化显示,hCG处理后,膜联蛋白A5(ANXA5)(一种GnRH的生物标志物)在颗粒-黄体细胞中表达,这表明hCG处理可诱导GnRH作用。 hCG增加了GnRH mRNA的水平,而GnRH激动剂(GnRHa)的处理增加了颗粒细胞原代培养物中ANXA5 mRNA的水平。 GnRH(10 –7 M)或GnRHa(醋酸阿替瑞林,10 -8 M)与hCG的同时孵育可在3小时的孵育时间内抑制孕激素的合成。促黄体生成素受体(LHR)和促卵泡激素受体(FSHR)的mRNA表达分别被hCG和GnRHa协同刺激和抑制。 GnRHa刺激p21表达,而GnRHa和hCG协同降低p27和FOXO1的mRNA表达水平。这些数据表明由LH诱导的GnRH可能对LH介导的颗粒细胞的黄体化起作用。另外,ANXA5可能参与了GnRH的作用。 GnRH-ANXA5将是细胞分化的重要机制。

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