重编程
诱导多能干细胞
细胞生物学
干细胞
体细胞
胚胎干细胞
生物
Wnt信号通路
细胞分化
胚状体
生殖系发育
生殖细胞
表观遗传学
遗传学
细胞
信号转导
基因
作者
Chika Yamashiro,Kotaro Sasaki,Shihori Yokobayashi,Yoji Kojima,Mitinori Saitou
出处
期刊:Nature Protocols
[Nature Portfolio]
日期:2020-03-30
卷期号:15 (4): 1560-1583
被引量:77
标识
DOI:10.1038/s41596-020-0297-5
摘要
The human germ-cell lineage originates as human primordial germ cells (hPGCs). hPGCs undergo genome-wide epigenetic reprogramming and differentiate into oogonia or gonocytes, precursors for oocytes or spermatogonia, respectively. Here, we describe a protocol to differentiate human induced pluripotent stem cells (hiPSCs) into oogonia in vitro. hiPSCs are induced into incipient mesoderm-like cells (iMeLCs) using activin A and a WNT pathway agonist. iMeLCs, or, alternatively, hPSCs cultured with divergent signaling inhibitors, are induced into hPGC-like cells (hPGCLCs) in floating aggregates by cytokines including bone morphogenic protein 4. hPGCLCs are aggregated with mouse embryonic ovarian somatic cells to form xenogeneic reconstituted ovaries, which are cultured under an air-liquid interface condition for ~4 months for hPGCLCs to differentiate into oogonia and immediate precursory states for oocytes. To date, this is the only approach that generates oogonia from hPGCLCs. The protocol is suitable for investigating the mechanisms of hPGC specification and epigenetic reprogramming.
科研通智能强力驱动
Strongly Powered by AbleSci AI