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首页> 外文期刊>Frontiers in Cell and Developmental Biology >Induced Pluripotent Stem Cells Derived From Two Idiopathic Azoospermia Patients Display Compromised Differentiation Potential for Primordial Germ Cell Fate
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Induced Pluripotent Stem Cells Derived From Two Idiopathic Azoospermia Patients Display Compromised Differentiation Potential for Primordial Germ Cell Fate

机译:衍生自两个特发性偶氮患者患者的诱导多能干细胞显示原始胚芽细胞命运的受损分化潜力

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摘要

At present, the etiology of most non-obstructive azoospermia (NOA) remains unclear. In vitro generation of patient-specific induced pluripotent stem cells (iPSCs) is an effective approach for exploring the mechanisms of human disease. Here, we established iPSCs from two patients with idiopathic NOA and differentiated them into primordial germ cell-like cells (PGCLCs) in vitro. Compared with iPSCs derived from normal fertile men, the NOA patient-specific iPSCs show decreased efficiency of PGCLC formation in vitro. Particularly, the embryoids derived from NOA patient-specific iPSCs show defects in the expression of early PGC genes. The transcriptome analysis reveals the expression patterns of key human PGC genes are generally similar in PGCLCs differentiated from all iPSC lines, and the differentially expressed genes (DEGs) were enriched with gene ontology (GO) of cell cycle and apoptosis regulation. Moreover, the PGCLCs derived from NOA patient-specific iPSCs might have initiated epigenetic reprogramming at a very early stage. Thus, the NOA patient-specific iPSCs exhibit poor response to germ cell induction in vitro, which may be related to the regulation of apoptotic process. These findings provide a foundation for future research on mechanism of male infertility.
机译:目前,大多数非阻塞性血吸虫(NOA)的病因仍然不清楚。体外产生患者特异性诱导的多能干细胞(IPSC)是探索人类疾病机制的有效方法。在这里,我们从两名特发性NOA的患者建立了IPSCS,并将其分化为体外原始生殖细胞样细胞(PGCLC)。与源自普通肥沃男性的IPSC相比,NOA患者特异性IPSCS显示出体外PGCLC形成的效率降低。特别地,衍生自NOA患者特异性IPSCs的胚性显示出早期PGC基因表达的缺陷。转录组分析揭示了关键人PGC基因的表达模式通常在与所有IPSC线分化的PGCLC中通常相似,并且差异表达的基因(DEGS)富含细胞循环和凋亡调节的基因本体(GO)。此外,来自NOA患者特异性IPSCs的PGCLC可能在很早的阶段启动了表观遗传学重编程。因此,NOA患者特异性IPSCs对体外生殖细胞诱导的反应不良,这可能与凋亡过程的调节有关。这些调查结果为未来的男性不孕症的机制研究提供了基础。

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