The ontogeny of cKIT+ human primordial germ cells proves to be a resource for human germ line reprogramming, imprint erasure and in vitro differentiation

被引:139
作者
Gkountela, Sofia [1 ,2 ]
Li, Ziwei [1 ,2 ]
Vincent, John J. [1 ,2 ]
Zhang, Kelvin X. [3 ]
Chen, Angela [4 ]
Pellegrini, Matteo [1 ]
Clark, Amander T. [1 ,2 ,5 ]
机构
[1] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Biol Chem, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
关键词
STEM-CELLS; C-KIT; FETAL; PLURIPOTENT; EXPRESSION; SPECIFICATION; 5-HYDROXYMETHYLCYTOSINE; METHYLATION; DERIVATION; PROTEINS;
D O I
10.1038/ncb2638
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The generation of research-quality, clinically relevant cell types in vitro from human pluripotent stem cells requires a detailed understanding of the equivalent human cell types. Here we analysed 134 human embryonic and fetal samples from 6 to 20 developmental weeks and identified the stages at which cKIT(+) primordial germ cells (PGCs), the precursors of gametes, undergo whole-genome epigenetic reprogramming with global depletion of 5mC, H3K27me3 and H2A.Z, and the time at which imprint erasure is initiated and 5hmC is present. Using five alternative in vitro differentiation strategies combined with single-cell microfluidic analysis and a bona fide human cKIT(+) PGC signature, we show the stage of cKIT(+) PGC formation in the first 16 days of differentiation. Taken together, our study creates a resource of human germ line ontogeny that is essential for future studies aimed at in vitro differentiation and unveiling the mechanisms necessary to pass human DNA from one generation to the next.
引用
收藏
页码:113 / U247
页数:18
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