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Differentiation of Induced Pluripotent Stem Cells into Male Germ CellsIn Vitrothrough Embryoid Body Formation and Retinoic Acid or Testosterone Induction

机译:通过胚状体形成和视黄酸或睾丸激素的诱导体外诱导多能干细胞分化为雄性生殖细胞。

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Generation of germ cells from pluripotent stem cellsin vitrocould 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 cellsin 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 ofStra8,Odf2,Act, andPrm1was upregulated in iPS cells by retinoic acid or testosterone induction, whereasOct-4transcription 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 cellsin vitrothrough embryoid body formation and retinoic acid or testosterone induction.
机译:从多能干细胞体外产生生殖细胞可能在治疗不育症中有很大的应用,并为揭示控制配子发生的分子机制提供了一个极好的模型。在这项研究中,我们探索了小鼠诱导的多能干(iPS)细胞向雄性生殖细胞的分化潜能。胚状体形成和视黄酸/睾丸激素诱导被用于促进小鼠iPS细胞体外分化为雄性生殖细胞。进行定量RT-PCR和免疫荧光来表征iPS细胞分化过程,特别是雄性生殖细胞相关基因的时间表达谱不同。包括MVH,CDH1和SCP3在内的蛋白质表达显着增加。通过视黄酸或睾丸激素的诱导,iPS细胞中Stra8,Odf2,Act和Prm1的mRNA表达上调,而与对照相比,这些细胞中的Oct-4转录降低。还在EB培养基中测量了激素。流式细胞仪分析DNA含量表明,iPS细胞可通过视黄酸或睾丸激素处理分化为单倍体细胞。总体而言,我们的研究结果表明,小鼠iPS细胞具有通过类胚体形成,视黄酸或睾丸激素诱导体外分化为雄性生殖细胞的能力。

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