味觉受体1型成员3调节西方饮食诱导的男性不育。

IF 3.9 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hobin Seong , Jae Won Song , Keon-Hee Lee , Goo Jang , Dong-Mi Shin , Woo-Jeong Shon
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引用次数: 0

摘要

西方饮食(WD)的特点是大量摄入脂肪和含糖饮料,是男性生殖功能障碍的危险因素。然而,这背后的分子机制尚不清楚。味觉受体1型成员3 (TAS1R3)被WD的配体激活,在口腔外组织,特别是睾丸中高度表达。在这里,我们研究了摄入WD对男性生殖的影响,以及TAS1R3是否介导WD引起的男性生殖损伤。雄性C57BL/6 J野生型(WT)和Tas1r3敲除型(KO)小鼠分别饲喂正常饮食和白水(ND)或60% %高脂饮食和30% % (w/v)蔗糖水(WD) 18 周(n = 7-9/组)。在Tas1r3过表达的WT小鼠中,长期食用WD会显著降低精子数量、活力和睾丸形态,而Tas1r3 KO小鼠则不会受到WD诱导的生殖损伤。睾丸转录组分析显示,在wd喂养的Tas1r3 KO小鼠中,amp活化蛋白激酶(AMPK)信号下调,AMPK靶向核受体4A1 (Nr4a1)表达显著升高。体外研究进一步证实,在间质细胞中,Tas1r3敲低可防止高葡萄糖、高果糖、高棕榈酸水平引起的Nr4a1及下游类固醇基因(Star、Cyp11a1、Cyp17a1、Hsd3b1)的抑制,维持睾酮水平。此外,我们分析了公共人类数据集,以评估我们研究结果的临床意义,并证实TAS1R3与男性不育相关疾病之间存在显著关联。我们的研究结果表明,TAS1R3通过AMPK/NR4A1信号调节wd诱导的男性生殖功能障碍,可能成为男性不育的新治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Taste receptor type 1 member 3 regulates Western diet-induced male infertility

Western diet (WD), characterized by a high intake of fats and sugary drinks, is a risk factor for male reproductive impairment. However, the molecular mechanisms underlying this remain unclear. Taste receptor type 1 member 3 (TAS1R3), activated by ligands of WD, is highly expressed in extra-oral tissues, particularly in the testes. Here, we investigated to determine the effects of WD intake on male reproduction and whether TAS1R3 mediates WD-induced impairment in male reproduction. Male C57BL/6 J wild-type (WT) and Tas1r3 knockout (KO) mice were fed either a normal diet and plain water (ND) or a 60 % high-fat-diet and 30 % (w/v) sucrose water (WD) for 18 weeks (n = 7–9/group). Long-term WD consumption significantly impaired sperm count, motility and testicular morphology in WT mice with marked Tas1r3 overexpression, whereas Tas1r3 KO mice were protected from WD-induced reproductive impairment. Testicular transcriptome analysis revealed downregulated AMP-activated protein kinase (AMPK) signaling and significantly elevated AMPK-targeted nuclear receptor 4A1 (Nr4a1) expression in WD-fed Tas1r3 KO mice. In vitro studies further validated that Tas1r3 knockdown in Leydig cells prevented the suppression of Nr4a1 and downstream steroidogenic genes (Star, Cyp11a1, Cyp17a1, and Hsd3b1) caused by high glucose, fructose, and palmitic acid levels, and maintained the levels of testosterone. Additionally, we analyzed the public human dataset to assess the clinical implications of our findings and confirmed a significant association between TAS1R3 and male-infertility-related diseases. Our findings suggest that TAS1R3 regulates WD-induced male reproductive impairment via the AMPK/NR4A1 signaling and can be a novel therapeutic target for male infertility.

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来源期刊
CiteScore
11.00
自引率
2.10%
发文量
109
审稿时长
53 days
期刊介绍: BBA Molecular and Cell Biology of Lipids publishes papers on original research dealing with novel aspects of molecular genetics related to the lipidome, the biosynthesis of lipids, the role of lipids in cells and whole organisms, the regulation of lipid metabolism and function, and lipidomics in all organisms. Manuscripts should significantly advance the understanding of the molecular mechanisms underlying biological processes in which lipids are involved. Papers detailing novel methodology must report significant biochemical, molecular, or functional insight in the area of lipids.
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