染料木素通过调节kisspeptin受体和关键调节因子影响GT1-7细胞促性腺激素释放激素的分泌。

IF 2.1 4区 医学 Q3 ANDROLOGY
Jingyuan Xiong, Ye Tian, Aru Ling, Zhenmi Liu, Li Zhao, Guo Cheng
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引用次数: 7

摘要

流行病学研究表明,染料木素是一种来自大豆的异黄酮类植物雌激素,影响内分泌和生殖系统,并改变青春期的发生。给小鼠注射染料木素可以影响与促性腺激素释放激素(GnRH)分泌相关的下丘脑神经元的电生理,促性腺激素释放激素(GnRH)是下丘脑-垂体-性腺(HPG)轴的关键组成部分,控制激素释放和生殖成熟。但染料木素是否直接影响GnRH特异性神经元分泌GnRH还有待进一步研究。本研究招募小鼠下丘脑GT1-7神经元作为GnRH表达模型,直接评价染料木素对GnRH释放的影响及其机制。本研究结果表明染料木素处理降低了细胞活力,影响了细胞周期分布,诱导了GT1-7细胞凋亡。高浓度染料木素(20 μM)使GnRH分泌量较对照组显著增加122.4%。由于GnRH的释放受kisspeptin-neurokinin-dynorphin (KNDy)系统和包括SIRT1、PKCγ和MKRN3在内的调节因子的调控,因此研究了它们的转录和翻译。KNDy成分kisspeptin受体(Gpr54/Kissr)的mRNA和蛋白水平显著升高。与对照组相比,染料木素上调了Sirt1 mRNA水平,下调了Prkcg和Mkrn3的表达。因此,本研究提供了直接证据,表明染料木素治疗可以通过调节GT1-7细胞中的kisspeptin受体、SIRT1、PKCγ和MKRN3来影响GnRH的分泌。缩写:GnRH:促性腺激素释放激素;高压天然气:hypothalamic-pituitary-gonadal;KNDy: kisspeptin-neurokinin-dynorphin;LH:黄体生成素;促卵泡激素;ARC:弓状核;ER:雌激素受体;SIRT1:无声信息调节器1;PKCγ:蛋白激酶c γ; MKRN3: makorin无名指蛋白3;LC:致死浓度;PI:碘化丙啶;发射极耦合逻辑:化学发光;BCA:双醌酸测定法;PBS:磷酸盐缓冲盐水;CT:荧光达到阈值;PVDF:聚偏二氟乙烯。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genistein affects gonadotrophin-releasing hormone secretion in GT1-7 cells via modulating kisspeptin receptor and key regulators.

Epidemiological studies have shown that genistein, an isoflavonoid phytoestrogen from soybean, affects endocrine and reproductive systems and alters pubertal onset. Administration of genistein in mice could impact the electrophysiology of hypothalamic neurons associated with the secretion of gonadotropin-releasing hormone (GnRH), a key component of hypothalamic-pituitary-gonadal (HPG) axis that governs hormone release and reproductive maturation. However, whether genistein could directly influence GnRH secretion in GnRH-specific neurons requires further investigation. Here, mouse hypothalamic GT1-7 neurons were recruited as a GnRH-expressing model to directly evaluate the effect and mechanisms of genistein on GnRH release. Results from this study demonstrated that genistein treatment decreased cell viability, impacted cell cycle distribution, and induced apoptosis of GT1-7 cells. A high concentration of genistein (20 μM) significantly increased GnRH secretion by 122.4% compared to the control. Since GnRH release is regulated by components of the kisspeptin-neurokinin-dynorphin (KNDy) system and regulators including SIRT1, PKCγ, and MKRN3, their transcription and translation were examined. Significant increases were observed for the mRNA and protein levels of the KNDy component kisspeptin receptor (Gpr54/Kissr). Compared to the control, genistein treatment upregulated the level of Sirt1 mRNA level, while it downregulated Prkcg and Mkrn3 expression. Therefore, this study provided direct evidence that genistein treatment could affect GnRH secretion by modulating kisspeptin receptors, SIRT1, PKCγ and MKRN3 in GT1-7 cells.Abbreviations: GnRH: gonadotropin-releasing hormone; HPG: hypothalamic-pituitary-gonadal; KNDy: kisspeptin-neurokinin-dynorphin; LH: luteinizing hormone; FSH: follicle-stimulating hormone; ARC: arcuate nucleus; ER: estrogen receptor; SIRT1: silent information regulator 1; PKCγ: protein kinase c γ: MKRN3: makorin ring finger protein 3; LC: lethal concentration; PI: propidium iodide; ECL: chemiluminescence; BCA: bicinchoninic acid assay; PBS: phosphate-buffered saline; CT: fluorescence reached threshold; PVDF: polyvinylidene difluoride.

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来源期刊
CiteScore
4.30
自引率
4.20%
发文量
27
审稿时长
>12 weeks
期刊介绍: Systems Biology in Reproductive Medicine, SBiRM, publishes Research Articles, Communications, Applications Notes that include protocols a Clinical Corner that includes case reports, Review Articles and Hypotheses and Letters to the Editor on human and animal reproduction. The journal will highlight the use of systems approaches including genomic, cellular, proteomic, metabolomic, bioinformatic, molecular, and biochemical, to address fundamental questions in reproductive biology, reproductive medicine, and translational research. The journal publishes research involving human and animal gametes, stem cells, developmental biology and toxicology, and clinical care in reproductive medicine. Specific areas of interest to the journal include: male factor infertility and germ cell biology, reproductive technologies (gamete micro-manipulation and cryopreservation, in vitro fertilization/embryo transfer (IVF/ET) and contraception. Research that is directed towards developing new or enhanced technologies for clinical medicine or scientific research in reproduction is of significant interest to the journal.
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