| Literature DB >> 29073541 |
Shou-Long Deng1, Zhi-Peng Wang2, Cheng Jin2, Xiao-Long Kang3, Aalia Batool2, Yan Zhang1, Xiao-Yu Li2, Xiu-Xia Wang1, Su-Ren Chen1, Chawn-Shang Chang4, C Yan Cheng5, Zheng-Xing Lian6, Yi-Xun Liu7.
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 10-7 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.Entities:
Keywords: Leydig cell; Melatonin; Sertoli cell; Sheep; Testosterone
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Year: 2017 PMID: 29073541 DOI: 10.1016/j.theriogenology.2017.10.025
Source DB: PubMed Journal: Theriogenology ISSN: 0093-691X Impact factor: 2.740