Clark Amander T
Department of Obstetrics, Gynecology and Reproductive Sciences, Program in Development and Stem Cell Biology, University of California at San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA.
Soc Reprod Fertil Suppl. 2007;63:77-86.
Germ cells are absolutely essential for fertility. Aberrant germ cell development can result in abnormal gonadal function, incomplete embryogenesis and infertility, or germ cell tumors. Our understanding of the molecular regulation of normal germ cell development in mammals has progressed significantly due to the utility of the mouse as a genetic model system. However, the molecular regulation of human germ cell development is almost completely unknown due to the historical lack of a malleable model. The purpose of this review is to compare the cell-based events leading up to the specification of the germ cell lineage in both mice and humans and to discuss some of the key signaling pathways that have recently been identified, which regulate germ cell specification. In addition, the new cell-based models for differentiating germ cells from both mouse and human embryonic stem cells (ESCs) will be summarized.
生殖细胞对于生育能力至关重要。生殖细胞发育异常可导致性腺功能异常、胚胎发育不全和不育,或引发生殖细胞肿瘤。由于小鼠作为遗传模型系统的实用性,我们对哺乳动物正常生殖细胞发育的分子调控的理解有了显著进展。然而,由于历史上缺乏可塑模型,人类生殖细胞发育的分子调控几乎完全未知。本综述的目的是比较小鼠和人类中导致生殖细胞谱系特化的基于细胞的事件,并讨论最近发现的一些调节生殖细胞特化的关键信号通路。此外,还将总结从小鼠和人类胚胎干细胞(ESC)分化出生殖细胞的新的基于细胞的模型。