Hua Jinlian, Zhu Haijing, Pan Shaohui, Liu Chao, Sun Junwei, Ma Xiaoling, Dong Wuzi, Liu Weishuai, Li Wei
College of Veterinary Medicine, Shaanxi Centre of Stem Cells Engineering & Technology, Key Lab for Reproductive Physiology & Embryo Biotechnology-Agriculture Ministry of China, Northwest A&F University, Yangling, Shaanxi, People's Republic of China.
Cell Reprogram. 2011 Apr;13(2):133-44. doi: 10.1089/cell.2010.0047.
Male germline stem cells (mGSCs) are stem cells present in male testis responsible for spermatogenesis during their whole life. Studies have shown that mGSCs can be derived in vitro and resemble embryonic stem cells (ESCs) properties both in the mouse and humans. However, little is know about these cells in domestic animals. Here we report the first successful establishment of goat GSCs derived from 2-5-month fetal testis, and developmental potential assay of these cells both in vitro and in vivo. These cells express pluripotent markers such as Oct4, Sox2, C-myc, and Tert when cultured as human ESCs conditions. Embryoid bodies (EBs) formed by goat mGSCs were induced with 2 × 10(-6) M retinoic acid (RA). Immunofluorescence analysis showed that some cells inside of the EBs were positive for meiosis marker-SCP3, STRA8, and germ cell marker-VASA, and haploid marker-FE-J1, PRM1, indicating their germ cell lineage differentiation. Some cells become elongated sperm-like cells after induction. Approximately 34.88% (30/86) embryos showed cleavage and four embryos were cultured on murine fibroblast feeder and formed small embryonic stem like colonies. However, most stalled at four-cell stage after intracytoplasmic sperm injection (ICSI) of these cells. Transplantation of DAPI labeled mGSCs into the seminiferous tubules of busulfan-treated mice, and showed that mGSCs can colonize, self-renew, and differentiate into germ cells. Thus, we have established a goat GSC cell line and these cells could be differentiated into sperm-like cells in vivo and sperms in vitro, providing a promising platform for generation of transgenic goat for production of specific humanized proteins.
雄性生殖系干细胞(mGSCs)是存在于雄性睾丸中的干细胞,负责其一生的精子发生。研究表明,mGSCs可以在体外获得,并且在小鼠和人类中都具有类似于胚胎干细胞(ESCs)的特性。然而,对于家畜中的这些细胞知之甚少。在此,我们报告了首次成功建立源自2至5个月龄胎儿睾丸的山羊生殖系干细胞(GSCs),并对这些细胞进行了体内外发育潜能分析。当在培养人类胚胎干细胞的条件下培养时,这些细胞表达多能性标志物,如Oct4、Sox2、C-myc和Tert。用2×10⁻⁶ M视黄酸(RA)诱导山羊mGSCs形成胚状体(EBs)。免疫荧光分析表明,EBs内部的一些细胞对减数分裂标志物-SCP3、STRA8以及生殖细胞标志物-VASA和单倍体标志物-FE-J1、PRM1呈阳性,表明它们向生殖细胞谱系分化。诱导后一些细胞变成了细长的精子样细胞。大约34.88%(30/86)的胚胎出现了卵裂,并且有4个胚胎在小鼠成纤维细胞饲养层上培养并形成了小的胚胎干细胞样集落。然而,在对这些细胞进行胞浆内精子注射(ICSI)后,大多数胚胎停滞在四细胞阶段。将用DAPI标记的mGSCs移植到白消安处理的小鼠的生精小管中,结果表明mGSCs可以定植、自我更新并分化为生殖细胞。因此,我们建立了山羊GSC细胞系,并且这些细胞可以在体内分化为精子样细胞,在体外分化为精子,为生产特定人源化蛋白质的转基因山羊的产生提供了一个有前景的平台。