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促黄体激素释放激素增加 kisspeptin 在促黄体激素释放激素分泌神经元细胞系中的表达和分泌。

Kisspeptin increases GnRH mRNA expression and secretion in GnRH secreting neuronal cell lines.

机构信息

Department of Pediatrics, Division of Endocrinology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

出版信息

Mol Cell Endocrinol. 2009 Nov 13;311(1-2):126-34. doi: 10.1016/j.mce.2009.06.011. Epub 2009 Jul 1.

Abstract

Kisspeptins, and their G-protein coupled receptor 54 (GPR54), are key components in the regulation of gonadotropin-releasing hormone (GnRH) secretion in humans and other mammals. Several studies demonstrate that the central or systemic administration of kisspeptin increases GnRH and gonadotropin secretion in both prepubertal and adult animals; however, the cellular targets and intracellular mechanisms of action in the central reproductive axis are unclear. In this study, we documented the presence of GPR54 in two GnRH secreting neuronal cell lines (GT1-7 and GN11). Kisspeptin treatment increases GnRH secretion and GnRH mRNA levels in a dose and time dependent manner. 10(-9)M kisspeptin maximally stimulated GnRH secretion by 2-fold and GnRH mRNA levels up to 4-fold after 4h of treatment in both cell lines. Negative regulation by 17beta-estradiol of GnRH secretion and GnRH mRNA was antagonized by kisspeptin. Co-treatment with kisspeptin and 17beta-estradiol increased GnRH secretion by 2-fold and GnRH mRNA by 4-fold over estradiol alone in both cell lines. Intracellular signaling pathway studies showed that an ERK1/2 MAPK inhibitor (PD98059) and a PI3K inhibitor, LY29402, attenuated the effects of kisspeptin on GnRH mRNA modulation. Furthermore, Western blot analysis showed that phosphorylation of both MAPK and Akt substrates increased with kisspeptin treatment. This work demonstrates that the kisspeptin-GPR54 system plays a significant role stimulating GnRH secretion and positive regulation of GnRH mRNA levels in GnRH neurons in culture, and also, demonstrates the activation of MAPK and Akt signaling pathways by kisspeptin in GT1-7 and GN11 cell lines.

摘要

kisspeptins 及其 G 蛋白偶联受体 54(GPR54)是调节人类和其他哺乳动物促性腺激素释放激素(GnRH)分泌的关键组成部分。多项研究表明, kisspeptin 的中枢或全身给药可增加 GnRH 和促性腺激素在青春期前和成年动物中的分泌;然而,中枢生殖轴中的细胞靶标和细胞内作用机制尚不清楚。在这项研究中,我们在两种 GnRH 分泌神经元细胞系(GT1-7 和 GN11)中记录了 GPR54 的存在。 kisspeptin 以剂量和时间依赖的方式增加 GnRH 的分泌和 GnRH mRNA 水平。在两种细胞系中, 10(-9)M kisspeptin 最大程度地刺激 GnRH 分泌增加 2 倍, GnRH mRNA 水平增加 4 倍,作用时间为 4 小时。 17β-雌二醇对 GnRH 分泌和 GnRH mRNA 的负调节作用被 kisspeptin 拮抗。 kisspeptin 与 17β-雌二醇共同处理可使两种细胞系中 GnRH 分泌增加 2 倍, GnRH mRNA 增加 4 倍,超过单独雌二醇的作用。细胞内信号通路研究表明, ERK1/2 MAPK 抑制剂(PD98059)和 PI3K 抑制剂 LY29402 减弱了 kisspeptin 对 GnRH mRNA 调节的作用。此外,Western blot 分析表明, MAPK 和 Akt 底物的磷酸化随 kisspeptin 处理而增加。这项工作表明, kisspeptin-GPR54 系统在培养的 GnRH 神经元中刺激 GnRH 分泌和 GnRH mRNA 水平的正调节中发挥重要作用,并且还表明 kisspeptin 在 GT1-7 和 GN11 细胞系中激活了 MAPK 和 Akt 信号通路。

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