| Literature DB >> 26993286 |
Shou-Long Deng1, Su-Ren Chen1, Zhi-Peng Wang1, Yan Zhang1, Ji-Xin Tang1, Jian Li1, Xiu-Xia Wang1, Jin-Mei Cheng1, Cheng Jin1, Xiao-Yu Li1, Bao-Lu Zhang2, Kun Yu2, Zheng-Xing Lian3, Guo-Shi Liu3, Yi-Xun Liu1.
Abstract
Promotion of spermatogonial stem cell (SSC) differentiation into functional sperms under in vitro conditions is a great challenge for reproductive physiologists. In this study, we observed that melatonin (10(-7) M) supplementation significantly enhanced the cultured SSCs differentiation into haploid germ cells. This was confirmed by the expression of sperm special protein, acrosin. The rate of SSCs differentiation into sperm with melatonin supplementation was 11.85 ± 0.93% which was twofold higher than that in the control. The level of testosterone, the transcriptions of luteinizing hormone receptor (LHR), and the steroidogenic acute regulatory protein (StAR) were upregulated with melatonin treatment. At the early stage of SSCs culture, melatonin suppressed the level of cAMP, while at the later stage, it promoted cAMP production. The similar pattern was observed in testosterone content. Expressions for marker genes of meiosis anaphase, Dnmt3a, and Bcl-2 were upregulated by melatonin. In contrast, Bax expression was downregulated. Importantly, the in vitro-generated sperms were functional and they were capable to fertilize oocytes. These fertilized oocytes have successfully developed to the blastula stage.Entities:
Keywords: Suffolk lambs; haploid germ cells; in vitro SSCs culture system; melatonin
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Year: 2016 PMID: 26993286 DOI: 10.1111/jpi.12327
Source DB: PubMed Journal: J Pineal Res ISSN: 0742-3098 Impact factor: 13.007