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利用萨能奶山羊雄性生殖细胞体外产生功能性单倍体精子细胞。

In vitro production of functional haploid sperm cells from male germ cells of Saanen dairy goat.

作者信息

Deng Shoulong, Wang Xiuxia, Wang Zhipeng, Chen Suren, Wang Yuqian, Hao Xiaoxia, Sun Tiecheng, Zhang Yi, Lian Zhengxing, Liu Yixun

机构信息

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

Laboratory of Animal Genetics and Breeding, College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China; Department of Animal Sciences, Georg-August-Universität Göttingen, Göttingen, 37075, Germany.

出版信息

Theriogenology. 2017 Mar 1;90:120-128. doi: 10.1016/j.theriogenology.2016.12.002. Epub 2016 Dec 2.

Abstract

The dairy goat is an important economic animal. Studies on in vitro differentiation of dairy goat spermatogonial stem cells (SSCs) could understand the molecular mechanisms for detecting mammalian sperm generation and innovative transgenetics. This study established an in vitro differentiation system for Saanen dairy goat SSCs. After 35 days incubation, single flagellum sperm-like cells with late round spermatid (Sa2) morphologically and the ability to express sperm-specific protein acrosin is detected. DNA ploid analysis showed that addition of testosterone to the culture system significantly improved the differentiation efficiency (P < 0.05) of haploid cells, and stimulated the post-meiotic gene (Tnp1, Tnp2 and Prm1) expression. A green fluorescent protein expressed in the morula was observed after transfection of the green fluorescent protein (GFP) vector with a round spermatid microinjection into the oocyte at metaphase II-stage. This study optimized activated method of the goat oocytes injected with round spermatids in vitro. This method increases the reconstructed embryonic development rate. These results suggest that testosterone boosts the efficiency of haploid cell differentiation in Saanen dairy goat testicular cells in the in vitro differentiation system. After optimization of activated and injection methods, fertility and embryonic were improved.

摘要

奶山羊是一种重要的经济动物。对奶山羊精原干细胞(SSCs)体外分化的研究有助于了解哺乳动物精子生成检测和创新转基因技术的分子机制。本研究建立了萨能奶山羊SSCs的体外分化体系。培养35天后,检测到形态上类似晚期圆形精子细胞(Sa2)且具有表达精子特异性蛋白顶体素能力的单鞭毛精子样细胞。DNA倍性分析表明,在培养体系中添加睾酮可显著提高单倍体细胞的分化效率(P < 0.05),并刺激减数分裂后基因(Tnp1、Tnp2和Prm1)的表达。将绿色荧光蛋白(GFP)载体转染至圆形精子细胞后,在第二次减数分裂中期将其显微注射到卵母细胞中,在桑椹胚中观察到绿色荧光蛋白的表达。本研究优化了体外注射圆形精子细胞的山羊卵母细胞激活方法。该方法提高了重构胚胎的发育率。这些结果表明,在体外分化体系中,睾酮可提高萨能奶山羊睾丸细胞中单倍体细胞的分化效率。经过激活和注射方法的优化,生育能力和胚胎质量得到了改善。

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