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褪黑素在与支持细胞共培养时可促进绵羊睾丸间质细胞睾酮分泌。

Melatonin promotes sheep Leydig cell testosterone secretion in a co-culture with Sertoli cells.

作者信息

Deng Shou-Long, Wang Zhi-Peng, Jin Cheng, Kang Xiao-Long, Batool Aalia, Zhang Yan, Li Xiao-Yu, Wang Xiu-Xia, Chen Su-Ren, Chang Chawn-Shang, Cheng C Yan, Lian Zheng-Xing, Liu Yi-Xun

机构信息

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, PR China.

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, PR China; University of the Chinese Academy of Sciences, Beijing 100101, PR China.

出版信息

Theriogenology. 2018 Jan 15;106:170-177. doi: 10.1016/j.theriogenology.2017.10.025. Epub 2017 Oct 17.

Abstract

Leydig cells synthesize and secrete testosterone, and are regulated by Sertoli cells. These two cell types may work together to regulate testicular androgen production. Studies have shown that Leydig cell androgen synthesis can be dramatically enhanced by Sertoli cells in the presence of melatonin, which can regulate the secretory function of Leydig and Sertoli cells. However, the molecular mechanism of melatonin-regulated Leydig cell androgen production via Sertoli cells remains unclear. Here, we found that 10 M melatonin increased testosterone production in co-cultured Leydig and Sertoli cells isolated from sheep. Melatonin increased the expression of stem cell factor and insulin-like growth factor-1 and decreased estrogen synthesis in Sertoli cells. Melatonin promoted insulin-like growth factor-1 and decreased estrogen content via the membrane melatonin receptor 1. It also enhanced stem cell factor expression via the retinoic acid receptor-related orphan receptor alpha. Addition of PD98059, a MEK inhibitor, to Sertoli cell culture demonstrated that the melatonin upregulation of insulin-like growth factor-1 and downregulation of estrogen may be through the MEK/extracellular signal-regulated kinase pathway. Together, these results suggest that melatonin may function through modulating melatonin receptor 1-regulated insulin-like growth factor-1 expression, as well as melatonin receptor 1-induced suppression of estrogen synthesis to increase androgen production in co-cultured Leydig and Sertoli cells.

摘要

睾丸间质细胞合成并分泌睾酮,且受支持细胞调节。这两种细胞类型可能共同作用来调节睾丸雄激素的产生。研究表明,在褪黑素存在的情况下,支持细胞可显著增强睾丸间质细胞的雄激素合成,褪黑素可调节睾丸间质细胞和支持细胞的分泌功能。然而,褪黑素通过支持细胞调节睾丸间质细胞雄激素产生的分子机制仍不清楚。在此,我们发现10 μM褪黑素可增加从绵羊分离的共培养睾丸间质细胞和支持细胞中的睾酮生成。褪黑素增加了支持细胞中干细胞因子和胰岛素样生长因子-1的表达,并减少了雌激素合成。褪黑素通过膜褪黑素受体1促进胰岛素样生长因子-1并降低雌激素含量。它还通过视黄酸受体相关孤儿受体α增强干细胞因子表达。向支持细胞培养物中添加MEK抑制剂PD98059表明,褪黑素对胰岛素样生长因子-1的上调和对雌激素的下调可能是通过MEK/细胞外信号调节激酶途径。总之,这些结果表明,褪黑素可能通过调节褪黑素受体1介导的胰岛素样生长因子-1表达以及褪黑素受体1诱导的雌激素合成抑制来增加共培养的睾丸间质细胞和支持细胞中的雄激素产生。

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