| Literature DB >> 28457750 |
Li Li1, Ji Dong1, Liying Yan2, Jun Yong2, Xixi Liu2, Yuqiong Hu3, Xiaoying Fan1, Xinglong Wu1, Hongshan Guo1, Xiaoye Wang2, Xiaohui Zhu2, Rong Li2, Jie Yan2, Yuan Wei2, Yangyu Zhao2, Wei Wang2, Yixin Ren2, Peng Yuan2, Zhiqiang Yan2, Boqiang Hu1, Fan Guo1, Lu Wen1, Fuchou Tang4, Jie Qiao5.
Abstract
Human fetal germ cells (FGCs) are precursors to sperm and eggs and are crucial for maintenance of the species. However, the developmental trajectories and heterogeneity of human FGCs remain largely unknown. Here we performed single-cell RNA-seq analysis of over 2,000 FGCs and their gonadal niche cells in female and male human embryos spanning several developmental stages. We found that female FGCs undergo four distinct sequential phases characterized by mitosis, retinoic acid signaling, meiotic prophase, and oogenesis. Male FGCs develop through stages of migration, mitosis, and cell-cycle arrest. Individual embryos of both sexes simultaneously contain several subpopulations, highlighting the asynchronous and heterogeneous nature of FGC development. Moreover, we observed reciprocal signaling interactions between FGCs and their gonadal niche cells, including activation of the bone morphogenic protein (BMP) and Notch signaling pathways. Our work provides key insights into the crucial features of human FGCs during their highly ordered mitotic, meiotic, and gametogenetic processes in vivo.Entities:
Keywords: Leydig cell; Sertoli cell; germ cell; germline; gonad; granulosa cell; oocyte; ovary; single-cell RNA sequencing; testis
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Year: 2017 PMID: 28457750 DOI: 10.1016/j.stem.2017.03.007
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633