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从携带复杂遗传异常的不育男性中诱导产生的 iPS 细胞可以生成原始生殖样细胞。

iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells.

机构信息

AP-HP, Université Paris-Saclay-Hôpital Antoine Béclère, Service d'Histologie, Embryologie et Cytogénétique, 92140, Clamart, France.

Faculté de Médecine, Université Paris-Saclay, 94270, Le Kremlin-Bicêtre, France.

出版信息

Sci Rep. 2022 Aug 22;12(1):14302. doi: 10.1038/s41598-022-17337-2.

Abstract

Despite increasing insight into the genetics of infertility, the developmental disease processes remain unclear due to the lack of adequate experimental models. The advent of induced pluripotent stem cell (iPSC) technology has provided a unique tool for in vitro disease modeling enabling major advances in our understanding of developmental disease processes. We report the full characterization of complex genetic abnormalities in two infertile patients with either azoospermia or XX male syndrome and we identify genes of potential interest implicated in their infertility. Using the erythroblasts of both patients, we generated primed iPSCs and converted them into a naive-like pluripotent state. Naive-iPSCs were then differentiated into primordial germ-like cells (PGC-LCs). The expression of early PGC marker genes SOX17, CD-38, NANOS3, c-KIT, TFAP2C, and D2-40, confirmed progression towards the early germline stage. Our results demonstrate that iPSCs from two infertile patients with significant genetic abnormalities are capable of efficient production of PGCs. Such in vitro model of infertility will certainly help identifying causative factors leading to early germ cells development failure and provide a valuable tool to explore novel therapeutic strategies.

摘要

尽管对不孕不育的遗传学有了更多的了解,但由于缺乏足够的实验模型,发育性疾病的过程仍不清楚。诱导多能干细胞(iPSC)技术的出现为体外疾病建模提供了独特的工具,使我们对发育性疾病过程的理解有了重大进展。我们报告了两名患有无精子症或 XX 男性综合征的不育患者的复杂遗传异常的全面特征,并鉴定了与他们不育相关的潜在感兴趣基因。使用这两名患者的红细胞,我们生成了初始 iPSC,并将其转化为类似原始的多能状态。然后,将原始 iPSC 分化为原始生殖细胞样细胞(PGC-LC)。早期 PGC 标记基因 SOX17、CD-38、NANOS3、c-KIT、TFAP2C 和 D2-40 的表达证实了向早期生殖细胞阶段的进展。我们的结果表明,两名具有明显遗传异常的不育患者的 iPSC 能够有效地产生 PGC。这种不育症的体外模型肯定有助于鉴定导致早期生殖细胞发育失败的致病因素,并为探索新的治疗策略提供了有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dba1/9395518/690ed7a1e355/41598_2022_17337_Fig1_HTML.jpg

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