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首页> 外文期刊>Human Reproduction >In vitro post-meiotic germ cell development from human embryonic stem cells.
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In vitro post-meiotic germ cell development from human embryonic stem cells.

机译:从人类胚胎干细胞体外减数分裂后生殖细胞发育。

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BACKGROUND: Investigating the mechanisms of human primordial germ cell (PGC) and gamete development are important for understanding the causes of infertility and effects of environmental chemicals on reproductive development. However, there are practical and ethical difficulties associated with obtaining human tissue in early development. The aim of this study was to investigate whether human embryonic stem cell-hESC-generated germ cells could provide an in vitro model of gamete development. METHOD: Human ESCs were differentiated as embryoid bodies (EBs) in vitro. Gene and protein marker expression profiles of EBs in different periods of culture were analysed by quantitative polymerase chain reaction (Q-PCR) and immunolocalization to monitor germ cell development. Secretion of hormones involved in germ cell maturation was measured, to detect the existence of a germ cell niche within EBs. RESULTS: Q-PCR revealed gene expression profiles consistent with PGC formation and germ cell development. A small population of post-meiotic spermatid cells were identified using sperm-specific antibodies (Protamine 1 and 1.97). Although gene expression profiles characteristic of oocyte development and follicle-like structures were detected, a committed oocyte with extra-cellular zona pellucida was not recognized with zona pellucida-specific monoclonal antibody. CONCLUSIONS: hESCs can form PGCs and post-meiotic spermatids in vitro, however, there remains doubt about oocyte development. Levels of steroid hormones produced by EBs were significant when compared with known values for a similar quantity of human testis, suggesting that hESC may intrinsically create a favourable hormonal niche for spermatogenesis.
机译:背景:调查人类原始生殖细胞(PGC)和配子发育的机制对于理解不育原因和环境化学物质对生殖发育的影响非常重要。然而,在早期发育中与获取人体组织相关联的实践和伦理上的困难。这项研究的目的是调查人类胚胎干细胞-hESC生成的生殖细胞是否可以提供配子发育的体外模型。方法:人类胚胎干细胞体外分化为胚状体(EBs)。通过定量聚合酶链反应(Q-PCR)和免疫定位来监测生殖细胞的发育,分析了不同培养阶段EB的基因和蛋白质标记表达谱。测量参与生殖细胞成熟的激素的分泌,以检测EB中生殖细胞小生境的存在。结果:Q-PCR显示与PGC形成和生殖细胞发育一致的基因表达谱。使用精子特异性抗体(鱼精蛋白1和1.97)鉴定了少数减数分裂后的精子细胞。尽管检测到了卵母细胞发育和卵泡状结构特征的基因表达谱,但是透明带透明性特异性单克隆抗体未识别出具有细胞外透明带的定型卵母细胞。结论:hESCs可以在体外形成PGC和减数分裂后的精子,但是,对于卵母细胞的发育仍存在疑问。与已知数量的人类睾丸的已知值相比,EB产生的类固醇激素水平显着,这表明hESC可能固有地为精子生成创造了一个有利的激素位。

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