凤凰素通过新的受体GPR173激活永生化GnRH和Kisspeptin神经元。

Q Biochemistry, Genetics and Molecular Biology
Molecular endocrinology Pub Date : 2016-08-01 Epub Date: 2016-06-06 DOI:10.1210/me.2016-1039
Alice K Treen, Vicky Luo, Denise D Belsham
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引用次数: 79

摘要

生殖功能是由kisspeptin (Kiss)和GnRH神经元协调。Phoenixin-20 amide (PNX)是最近发现的一种肽,可以增加垂体中gnrh刺激的LH分泌。然而,PNX在下丘脑中的作用、可能的信号通路和PNX受体尚未确定。mHypoA-GnRH/GFP和mHypoA-Kiss/GFP-3细胞系分别代表GnRH和Kiss神经元群体。在mHypoA-GnRH/GFP细胞模型中,PNX增加了GnRH和GnRH受体(GnRH- r) mRNA的表达以及GnRH的分泌。在mHypoA-Kiss/GFP-3细胞系中,PNX增加了Kiss1 mRNA的表达。CCAAT/增强子结合蛋白(C/EBP)-β、八聚体转录因子-1 (Oct-1)和cAMP反应元件结合蛋白(CREB)结合位点位于GnRH、GnRH- r和Kiss1基因的5'侧区。PNX降低了两种细胞模型中C/EBP-β mRNA的表达,增加了mHypoA-GnRH/GFP神经元中Oct-1 mRNA的表达。PNX在细胞模型中增加CREB磷酸化,在mHypoA-GnRH/GFP细胞模型中增加磷酸化- erk1 /2,而抑制cAMP/蛋白激酶A通路阻止PNX诱导GnRH和Kiss1 mRNA表达。重要的是,我们确定了G蛋白偶联受体GPR173在GnRH和kisspeptin细胞模型中都有强烈表达,GPR173的小干扰RNA敲低阻止了pnx介导的GnRH、GnRH- r和Kiss1 mRNA表达的上调和C/EBP-β mRNA表达的下调。PNX还增加了mHypoA-GnRH/GFP细胞中GPR173 mRNA的表达。综上所述,这些研究首次表明PNX通过GPR173通过CREB激活cAMP/蛋白激酶A通路,并可能通过C/EBP-β和/或Oct-1增加GnRH、GnRH- r和Kiss1基因的表达,最终对生殖功能产生刺激作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phoenixin Activates Immortalized GnRH and Kisspeptin Neurons Through the Novel Receptor GPR173.

Phoenixin Activates Immortalized GnRH and Kisspeptin Neurons Through the Novel Receptor GPR173.

Phoenixin Activates Immortalized GnRH and Kisspeptin Neurons Through the Novel Receptor GPR173.

Phoenixin Activates Immortalized GnRH and Kisspeptin Neurons Through the Novel Receptor GPR173.

Reproductive function is coordinated by kisspeptin (Kiss) and GnRH neurons. Phoenixin-20 amide (PNX) is a recently described peptide found to increase GnRH-stimulated LH secretion in the pituitary. However, the effects of PNX in the hypothalamus, the putative signaling pathways, and PNX receptor have yet to be identified. The mHypoA-GnRH/GFP and mHypoA-Kiss/GFP-3 cell lines represent populations of GnRH and Kiss neurons, respectively. PNX increased GnRH and GnRH receptor (GnRH-R) mRNA expression, as well as GnRH secretion, in the mHypoA-GnRH/GFP cell model. In the mHypoA-Kiss/GFP-3 cell line, PNX increased Kiss1 mRNA expression. CCAAT/enhancer-binding protein (C/EBP)-β, octamer transcription factor-1 (Oct-1), and cAMP response element binding protein (CREB) binding sites are localized to the 5' flanking regions of the GnRH, GnRH-R, and Kiss1 genes. PNX decreased C/EBP-β mRNA expression in both cell models and increased Oct-1 mRNA expression in the mHypoA-GnRH/GFP neurons. PNX increased CREB phosphorylation in both cell models and phospho-ERK1/2 in the mHypoA-GnRH/GFP cell model, whereas inhibiting the cAMP/protein kinase A pathway prevented PNX induction of GnRH and Kiss1 mRNA expression. Importantly, we determined that the G protein-coupled receptor, GPR173, was strongly expressed in both GnRH and kisspeptin cell models and small interfering RNA knockdown of GPR173 prevented the PNX-mediated up-regulation of GnRH, GnRH-R, and Kiss1 mRNA expression and the down-regulation of C/EBP-β mRNA expression. PNX also increased GPR173 mRNA expression in the mHypoA-GnRH/GFP cells. Taken together, these studies are the first to implicate that PNX acts through GPR173 to activate the cAMP/protein kinase A pathway through CREB, and potentially C/EBP-β and/or Oct-1 to increase GnRH, GnRH-R, and Kiss1 gene expression, ultimately having a stimulatory effect on reproductive function.

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来源期刊
Molecular endocrinology
Molecular endocrinology 医学-内分泌学与代谢
CiteScore
3.49
自引率
0.00%
发文量
0
审稿时长
12 months
期刊介绍: Molecular Endocrinology provides a forum for papers devoted to describing molecular mechanisms by which hormones and related compounds regulate function. It has quickly achieved a reputation as a high visibility journal with very rapid communication of cutting edge science: the average turnaround time is 28 days from manuscript receipt to first decision, and accepted manuscripts are published online within a week through Rapid Electronic Publication. In the 2008 Journal Citation Report, Molecular Endocrinology is ranked 16th out of 93 journals in the Endocrinology and Metabolism category, with an Impact Factor of 5.389.
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