Wang Xiaoman, Liao Tingting, Wan Cong, Yang Xiaoyu, Zhao Jiexiang, Fu Rui, Yao Zhaokai, Huang Yaping, Shi Yujia, Chang Gang, Zheng Yi, Luo Fang, Liu Zhaoting, Wang Yu, Mao Xinliang, Zhao Xiao-Yang
State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
PeerJ. 2019 Jan 9;6:e6143. doi: 10.7717/peerj.6143. eCollection 2019.
The mechanisms underlying human germ cell development and infertility remain largely unknown due to bioethical issues and the shortage of experimental materials. Therefore, an effective in vitro induction system of human primordial germ-like cells (hPGCLCs) from human pluripotent stem cells (hPSC) is in high demand. The current strategies used for the generation of hPGCLCs are not only costly but also difficult to perform at a large scale, thereby posing barriers to further research. In this study, we attempted to solve these problems by providing a new 3D culture system for hPGCLC differentiation.
The efficiency and relative yield of a methylcellulose (MC)-based 3D hPGCLC induction system were first compared with that of a conventional U96 system. Then, we examined the gene expression of germ cell marker genes and the key epigenetic modifications of the EpCAM-/INTEGRINα6-high cells from the 3D MC induction system and the U96 system via quantitative PCR and immunofluorescence. Finally, the reliability of the MC-based 3D hPGCLC induction system was evaluated via the generation of induced pluripotent stem cells (iPSCs) from the testicular cells of one patient with obstructive azoospermia (OA) and followed by the subsequent differentiation of iPSCs into the germ cell lineage.
In the present study, we demonstrated that the 3D MC induction system combined with low-cell attachment plates facilitated the generation of hPGCLCs at a large scale. We found that the hPGCLCs generated via the MC system shared similar characteristics to that via the U96 system in terms of the gene expression profiles, germ cell-specific markers, epigenetic modification states and cellular states. In addition, hPGCLCs from iPSCs derived from one OA patient were generated with high efficiency via the present 3D MC induction system.
The in vitro induction of hPGCLCs from human embryonic stem cells (hESCs)/human induced pluripotent stem cells (hiPSCs) has significant implications in exploring the underlying mechanisms of the origin and specification of hPGCs and the epigenetic programming of the human germ line as well as treating male infertility. Here, we developed a simple and efficient 3D induction system to generate hPGCLCs from hESCs/hiPSCs at a large scale, which facilitated the study of human germ cell development and stem cell-based reproductive medicine.
由于生物伦理问题和实验材料的短缺,人类生殖细胞发育和不育的潜在机制在很大程度上仍然未知。因此,人们迫切需要一种从人多能干细胞(hPSC)有效体外诱导人原始生殖样细胞(hPGCLC)的系统。目前用于生成hPGCLC的策略不仅成本高昂,而且难以大规模实施,从而为进一步研究带来了障碍。在本研究中,我们试图通过提供一种用于hPGCLC分化的新型三维培养系统来解决这些问题。
首先将基于甲基纤维素(MC)的三维hPGCLC诱导系统的效率和相对产量与传统的U96系统进行比较。然后,我们通过定量PCR和免疫荧光检测了来自三维MC诱导系统和U96系统的EpCAM-/整合素α6高表达细胞的生殖细胞标记基因的表达以及关键表观遗传修饰。最后,通过从一名梗阻性无精子症(OA)患者睾丸细胞中生成诱导多能干细胞(iPSC),随后将iPSC分化为生殖细胞谱系,评估了基于MC的三维hPGCLC诱导系统的可靠性。
在本研究中,我们证明了三维MC诱导系统与低细胞贴壁板相结合有助于大规模生成hPGCLC。我们发现,通过MC系统生成的hPGCLC在基因表达谱、生殖细胞特异性标记、表观遗传修饰状态和细胞状态方面与通过U96系统生成的hPGCLC具有相似的特征。此外,通过本三维MC诱导系统可高效地从一名OA患者来源的iPSC中生成hPGCLC。
从人胚胎干细胞(hESC)/人诱导多能干细胞(hiPSC)体外诱导hPGCLC对于探索hPGC起源和特化的潜在机制、人类生殖系的表观遗传编程以及治疗男性不育具有重要意义。在此,我们开发了一种简单有效的三维诱导系统,可从hESC/hiPSC大规模生成hPGCLC,这有助于人类生殖细胞发育研究和基于干细胞的生殖医学研究。