Single-Cell RNA-Seq Analysis Maps Development of Human Germline Cells and Gonadal Niche Interactions

被引:118
作者
Li, Li
Dong, Ji
Yan, Liying
Yong, Jun
Liu, Xixi
Hu, Yuqiong
Fan, Xiaoying
Wu, Xinglong
Guo, Hongshan
Wang, Xiaoye
Zhu, Xiaohui
Li, Rong
Yan, Jie
Wei, Yuan
Zhao, Yangyu
Wang, Wei
Ren, Yixin
Yuan, Peng
Yan, Zhiqiang
Hu, Boqiang
Guo, Fan
Wen, Lu
Tang, Fuchou
Qiao, Jie
机构
[1] Beijing Advanced Innovation Center for Genomics (ICG), College of Life Sciences, Department of Obstetrics and Gynecology, Third Hospital, Peking University, Beijing
[2] Biomedical Institute for Pioneering Investigation via Convergence and Center for Reproductive Medicine, Ministry of Education Key Laboratory of Cell Proliferation and Differentiation, Beijing
[3] Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing
[4] Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing
[5] Peking-Tsinghua Center for Life Sciences, Peking University, Beijing
基金
中国国家自然科学基金;
关键词
germ cell; germline; gonad; granulosa cell; Leydig cell; oocyte; ovary; Sertoli cell; single-cell RNA sequencing; testis;
D O I
10.1016/j.stem.2017.05.009
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:891 / 892
页数:2
相关论文
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[1]  
Li L, 2017, CELL STEM CELL, V20, P858, DOI 10.1016/j.stem.2017.03.007