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通过胚状体形成和维甲酸或睾酮诱导,将诱导多能干细胞体外分化为雄性生殖细胞。

Differentiation of induced pluripotent stem cells into male germ cells in vitro through embryoid body formation and retinoic acid or testosterone induction.

机构信息

Shanghai Human Sperm Bank, Department of Urology, Shanghai Institute of Andrology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200001, China.

出版信息

Biomed Res Int. 2013;2013:608728. doi: 10.1155/2013/608728. Epub 2012 Dec 30.

DOI:10.1155/2013/608728
PMID:23509752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3591174/
Abstract

Generation of germ cells from pluripotent stem cells in vitro could have great application for treating infertility and provides an excellent model for uncovering molecular mechanisms controlling gametogenesis. In this study, we explored the differentiation potential of mouse induced pluripotent stem (iPS) cells towards male germ cells. Embryoid body formation and retinoic acid/testosterone induction were applied to promote differentiation of mouse iPS cells into male germ cells in vitro. Quantitative RT-PCR and immunoflourescence were performed to characterize the iPS cell differentiation process, and notably there were different temporal expression profiles of male germ cell-associated genes. The expression of proteins, including MVH, CDH1, and SCP3, was remarkably increased. mRNA expression of Stra8, Odf2, Act, and Prm1 was upregulated in iPS cells by retinoic acid or testosterone induction, whereas Oct-4 transcription was reduced in these cells compared to the controls. Hormones were also measured in the EB medium. DNA content analysis by flow cytometry revealed that iPS cells could differentiate into haploid cells through retinoic acid or testosterone treatment. Collectively, our results suggest that mouse iPS cells possess the potency to differentiate into male germ cells in vitro through embryoid body formation and retinoic acid or testosterone induction.

摘要

体外多能干细胞向生殖细胞的分化可能在治疗不孕不育方面具有重要应用价值,并为揭示控制配子发生的分子机制提供了一个很好的模型。在这项研究中,我们探索了小鼠诱导多能干细胞(iPS)向雄性生殖细胞分化的潜能。通过胚状体形成和视黄酸/睾丸酮诱导,促进小鼠 iPS 细胞在体外向雄性生殖细胞分化。采用实时定量 RT-PCR 和免疫荧光技术对 iPS 细胞的分化过程进行了特征描述,值得注意的是,雄性生殖细胞相关基因的表达存在不同的时间表达谱。MVH、CDH1 和 SCP3 等蛋白的表达显著增加。视黄酸或睾丸酮诱导后,iPS 细胞中 Stra8、Odf2、Act 和 Prm1 的 mRNA 表达上调,而 Oct-4 转录则低于对照组。还在 EB 培养基中测量了激素。流式细胞术的 DNA 含量分析显示,iPS 细胞通过视黄酸或睾丸酮处理可以分化为单倍体细胞。总之,我们的结果表明,通过胚状体形成和视黄酸/睾丸酮诱导,小鼠 iPS 细胞具有在体外向雄性生殖细胞分化的潜能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/d85f8896e08c/BMRI2013-608728.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/69e0c25e3e0b/BMRI2013-608728.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/43f59fcbb351/BMRI2013-608728.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/3168e1f1cf7e/BMRI2013-608728.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/6b84947b07a7/BMRI2013-608728.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/ebed68a7ff0d/BMRI2013-608728.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/d85f8896e08c/BMRI2013-608728.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/69e0c25e3e0b/BMRI2013-608728.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/43f59fcbb351/BMRI2013-608728.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/3168e1f1cf7e/BMRI2013-608728.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/6b84947b07a7/BMRI2013-608728.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/ebed68a7ff0d/BMRI2013-608728.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bbc/3591174/d85f8896e08c/BMRI2013-608728.006.jpg

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