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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Apelin (APLN) and Apelin Receptor (APLNR) in Human Ovary: Expression, Signaling, and Regulation of Steroidogenesis in Primary Human Luteinized Granulosa Cells
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Apelin (APLN) and Apelin Receptor (APLNR) in Human Ovary: Expression, Signaling, and Regulation of Steroidogenesis in Primary Human Luteinized Granulosa Cells

机译:中卵巢中的Apelin(APLN)和阿糖蛋白受体(APLNR):原发性叶氏芽孢菌粒细胞中甾体素的表达,信号传导和调节

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摘要

Apelin (APLN) is a recently discovered adipokine involved in the regulation of various metabolic functions. Its receptor, APLNR, is expressed in reproductive tissues, however, its role in human ovarian cells is unknown. In this study, we identified APLN and APLNR in human ovarian follicles and analyzed their expression in granulosa cells and follicular fluid obtained from obese and nonobese patients, with or without polycystic ovary syndrome (PCOS). We also investigated the effect of APLN on steroidogenesis in cultured human luteinized granulosa cells (hGCs) from nonobese patients without PCOS. Using RT-PCR and immunoblotting, we found that APLN and APLNR were expressed in hGCs and cumulus and theca cells. We confirmed these data immunohistochemically and observed that APLNR and APLN are present in human oocytes at different stages of follicular development. In patients with PCOS, we observed that follicular fluid APLN concentration and granulosa cell APLN and APLNR mRNA expression was higher than that observed in control patients. In cultured hGCs from nonobese patients without PCOS, insulin-like growth factor 1 (IGF1) increased APLNR expression, and recombinant human APLN (APLN-13 and APLN-17) increased both basal and IGF1-induced steroid secretion. These effects on steroid production were reversed when cultured in the presence of ML221, an APLNR antagonist, which was associated with an increased 3beta-hydrosteroid dehydrogenase (HSD3B) protein concentration. We showed that these effects were dependent on the activation of the AKT and MAPK3/1 pathways using pharmacological inhibitors. Our results show that APLN and APLNR are present in human ovarian cells and APLN increases IGF1-induced steroidogenesis in granulosa cells through an increase in HSD3B protein expression and activation of the MAPK3/1 and Akt pathways. Therefore, APLN and APLNR may play a role in human follicular development and the pathogenesis of PCOS.
机译:Apelin(APLN)是最近发现的adipokine参与了各种代谢功能的调节。其受体APLNR在生殖组织中表达,然而,其在人类卵巢细胞中的作用是未知的。在这项研究中,我们鉴定了人卵巢卵泡中的APLN和APLNR,并分析了从玉米菌细胞和从肥胖和非患者获得的卵泡液中的表达,有或没有多囊卵巢综合征(PCOS)。我们还研究了APLN对没有PCOS的非同源患者培养的人类叶氏芽孢菌粒细胞(HGC)中的毒素发生的影响。使用RT-PCR和免疫印迹,我们发现APLN和APLNR以HGC和巨大和CONCA细胞表达。我们确认了免疫组织化学的这些数据,并观察到APLNR和APLN在滤泡发育的不同阶段存在于人卵母细胞中。在PCOS患者中,我们观察到,滤泡液Apln浓度和颗粒细胞Apln和Aplnr mRNA表达高于对照患者观察到的颗粒状细胞。在没有PCOS的非同源患者的培养HGC中,胰岛素样生长因子1(IGF1)增加APLNR表达,重组人APLN(APLN-13和APLN-17)增加了基础和IGF1诱导的类固醇分泌。当在ML221的存在下培养的APLNR拮抗剂存在时,这些对类固醇产生的影响逆转,这与增加的3Beta - 水质醇脱氢酶(HSD3B)蛋白质浓度相关。我们表明这些效应依赖于使用药理学抑制剂的AKT和MAPK3 / 1途径的激活。我们的结果表明,通过增加HSD3B蛋白表达和MAPK3 / 1和AKT途径的增加,APLN和APLNR中存在于人卵巢细胞中,APLN在颗粒细胞中增加IGF1诱导的甾体系。因此,APLN和APLNR可能在人类滤窗发育和PCOS的发病机制中起作用。

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