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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:人类卵巢中的Apelin(APLN)和Apelin受体(APLNR):原代人黄体化颗粒细胞中类固醇生成的表达,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)是最近发现的一种参与调节各种代谢功能的脂肪因子。它的受体APLNR在生殖组织中表达,但是在人类卵巢细胞中的作用尚不清楚。在这项研究中,我们鉴定了人类卵巢卵泡中的APLN和APLNR,并分析了它们在患有或不患有多囊卵巢综合征(PCOS)的肥胖和非肥胖患者的颗粒细胞和卵泡液中的表达。我们还调查了APLN对非PCOS非肥胖患者培养的人黄素化颗粒细胞(hGCs)中类固醇生成的影响。使用RT-PCR和免疫印迹,我们发现APLN和APLNR在hGC,卵丘和theca细胞中表达。我们通过免疫组织化学证实了这些数据,并观察到APLNR和APLN存在于卵泡发育不同阶段的人卵母细胞中。在PCOS患者中,我们观察到卵泡液中APLN的浓度以及颗粒细胞APLN和APLNR mRNA的表达高于对照组。在没有PCOS的非肥胖患者培养的hGC中,胰岛素样生长因子1(IGF1)增加了APLNR的表达,重组人APLN(APLN-13和APLN-17)增加了基础和IGF1诱导的类固醇分泌。在APLNR拮抗剂ML221的存在下培养时,对类固醇产生的这些作用被逆转,这与3β-氢类固醇脱氢酶(HSD3B)蛋白浓度升高相关。我们表明,这些作用依赖于使用药理抑制剂的AKT和MAPK3 / 1途径的激活。我们的结果表明APLN和APLNR存在于人类卵巢细胞中,并且APLN通过增加HSD3B蛋白表达以及激活MAPK3 / 1和Akt途径来增加IGF1诱导的颗粒细胞类固醇生成。因此,APLN和APLNR可能在人类卵泡发育和PCOS的发病机理中起作用。

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