Department of Anatomy and Cell Biology, Graduate School of Medicine, Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Cell. 2011 Aug 19;146(4):519-32. doi: 10.1016/j.cell.2011.06.052. Epub 2011 Aug 4.
The generation of properly functioning gametes in vitro requires reconstitution of the multistepped pathway of germ cell development. We demonstrate here the generation of primordial germ cell-like cells (PGCLCs) in mice with robust capacity for spermatogenesis. PGCLCs were generated from embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) through epiblast-like cells (EpiLCs), a cellular state highly similar to pregastrulating epiblasts but distinct from epiblast stem cells (EpiSCs). Reflecting epiblast development, EpiLC induction from ESCs/iPSCs is a progressive process, and EpiLCs highly competent for the PGC fate are a transient entity. The global transcription profiles, epigenetic reprogramming, and cellular dynamics during PGCLC induction from EpiLCs meticulously capture those associated with PGC specification from the epiblasts. Furthermore, we identify Integrin-β3 and SSEA1 as markers that allow the isolation of PGCLCs with spermatogenic capacity from tumorigenic undifferentiated cells. Our findings provide a paradigm for the first step of in vitro gametogenesis.
体外生成功能正常的配子需要重建生殖细胞发育的多步途径。我们在这里证明了具有强大精子发生能力的小鼠中原始生殖细胞样细胞 (PGCLC) 的生成。PGCLC 是通过类胚层细胞 (EpiLC) 从胚胎干细胞 (ESC) 和诱导多能干细胞 (iPSC) 生成的,EpiLC 是一种非常类似于着床前胚层但与胚层干细胞 (EpiSC) 不同的细胞状态。反映胚层的发育,EpiLC 从 ESC/iPSC 的诱导是一个渐进的过程,并且具有高度 PGC 命运潜能的 EpiLC 是一种短暂的实体。从 EpiLC 诱导 PGCLC 过程中的全局转录谱、表观遗传重编程和细胞动力学,细致地捕捉到与胚层中 PGC 特化相关的那些。此外,我们确定整合素-β3 和 SSEA1 作为标记,允许从致瘤未分化细胞中分离具有精子发生能力的 PGCLC。我们的发现为体外配子发生的第一步提供了范例。