Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Department for Reproductive Medicine, Ghent University Hospital, Ghent, Belgium.
Methods Mol Biol. 2024;2770:63-83. doi: 10.1007/978-1-0716-3698-5_6.
In the human fetal testis, fetal germ cells (FGCs) are progressively surrounded by supporting Sertoli cells inside seminiferous cords. During the second trimester, the FGCs develop asynchronously and can be observed in several stages of development. However, the mechanism that regulates the transition between the different developmental stages as well as the formation of spermatogonia is currently not well understood. For this, it is necessary to develop suitable isolation protocols and a platform for in vitro culture of FGCs of different stages. Here, we report a method to isolate distinct populations of FGCs and Sertoli cells from second trimester human testis using a panel of conjugated antibodies for THY1, PDPN, ALPL, KIT, and SUSD2 for fluorescence-activated cell sorting (FACS) followed by in vitro culture up to 7 days. This platform provides the base for cellular and molecular characterization of the different testicular cell populations to investigate the transition between FGCs and spermatogonia and shed some light on crucial processes of early human gametogenesis unknown until now.
在人类胎儿睾丸中,胎儿生殖细胞(FGC)逐渐被生精小管内的支持细胞包围。在妊娠中期,FGC 发育不同步,可以观察到几个发育阶段。然而,调节不同发育阶段之间的转变以及精原细胞形成的机制目前尚不清楚。为此,有必要开发合适的分离方案和体外培养不同阶段 FGC 的平台。在这里,我们报告了一种使用 THY1、PDPN、ALPL、KIT 和 SUSD2 等一系列共轭抗体通过荧光激活细胞分选(FACS)从妊娠中期人睾丸中分离不同群体的 FGC 和支持细胞的方法,然后进行体外培养,最多可达 7 天。该平台为不同睾丸细胞群体的细胞和分子特征提供了基础,以研究 FGC 和精原细胞之间的转变,并阐明目前为止未知的早期人类配子发生的关键过程。