Kereilwe O, Pandey K, Kadokawa H
Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi-shi, Yamaguchi-ken, 1677-1, Japan.
Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi-shi, Yamaguchi-ken, 1677-1, Japan.
Domest Anim Endocrinol. 2018 Jul;64:77-83. doi: 10.1016/j.domaniend.2018.04.002. Epub 2018 Apr 10.
We recently discovered that the orphan G-protein-coupled receptor (GPR) 61 colocalized with GnRH receptors (GnRHRs) on the surface of most of bovine gonadotrophs. A recent study suggested that ethanolamine plasmalogen (PI) is a ligand for GPR61 in mouse neuroblastoma. Therefore, this study evaluated the hypothesis that PI alters LH and FSH secretion from cultured bovine anterior pituitary (AP) cells. We prepared bovine AP cells from postpubertal heifers (26 mo old) and cultured the cells for 3.5 d. We treated the cells with increasing concentrations (0, 5, 50, 500, 5,000, 50,000, or 500,000 pg/mL) of phosphoethanolamine PI (PEPI) extracted from the bovine brain, or l-α-lysophosphatidylethanolamine PI (LEPI) extracted from the bovine brain, for 5 min before either no treatment or GnRH stimulation. The medium samples were harvested 2 h after culture for LH and FSH assays. Phosphoethanolamine PI (50-500 pg/mL) stimulated (P < 0.05) the basal secretion of FSH but not LH. Phosphoethanolamine PI at 50 pg/mL also enhanced (P < 0.05) GnRH-induced FSH secretion. However, higher doses (500-500,000 pg/mL) of PEPI suppressed GnRH-induced FSH secretion. Moreover, 50 to 500,000 pg/mL PEPI suppressed GnRH-induced LH secretion. None of the tested concentrations of LEPI showed any effect on basal or GnRH-induced LH or FSH secretion. Pretreatment with Sma and Mad pathway inhibitors suppressed FSH secretion induced by PEPI, whereas an extracellular signal-regulated kinase pathway inhibitor blocked the PEPI-induced suppression of GnRH-stimulated LH secretion. Therefore, PEPI, but not LEPI, extracted from the bovine brain, alters FSH and LH secretion from cultured AP cells. Further studies are required to decide whether PEPI binds to GPR61 and whether PEPI plays an important role in the control of gonadotropin secretion from gonadotrophs.
我们最近发现,孤儿G蛋白偶联受体(GPR)61与大多数牛促性腺激素细胞表面的促性腺激素释放激素受体(GnRHRs)共定位。最近一项研究表明,乙醇胺缩醛磷脂(PI)是小鼠神经母细胞瘤中GPR61的配体。因此,本研究评估了PI改变培养的牛垂体前叶(AP)细胞促黄体生成素(LH)和促卵泡生成素(FSH)分泌这一假说。我们从青春期后小母牛(26月龄)制备牛AP细胞,并将细胞培养3.5天。在不进行处理或GnRH刺激之前,我们用从牛脑中提取的浓度递增(0、5、50、500、5000、50000或500000 pg/mL)的磷酸乙醇胺PI(PEPI)或从牛脑中提取的l-α-溶血磷脂酰乙醇胺PI(LEPI)处理细胞5分钟。培养2小时后收集培养基样本用于LH和FSH检测。磷酸乙醇胺PI(50 - 500 pg/mL)刺激(P < 0.05)FSH的基础分泌,但不刺激LH的基础分泌。50 pg/mL的磷酸乙醇胺PI也增强(P < 0.05)GnRH诱导的FSH分泌。然而,更高剂量(500 - 500000 pg/mL)的PEPI抑制GnRH诱导的FSH分泌。此外,50至500000 pg/mL的PEPI抑制GnRH诱导的LH分泌。所测试的任何浓度的LEPI对基础或GnRH诱导的LH或FSH分泌均无影响。用Sma和Mad通路抑制剂预处理可抑制PEPI诱导的FSH分泌,而细胞外信号调节激酶通路抑制剂可阻断PEPI诱导的对GnRH刺激的LH分泌的抑制作用。因此,从牛脑中提取的PEPI而非LEPI可改变培养的AP细胞中FSH和LH的分泌。需要进一步研究来确定PEPI是否与GPR61结合,以及PEPI在控制促性腺激素细胞促性腺激素分泌中是否起重要作用。