Derivation of embryonic germ cells and male gametes from embryonic stem cells

被引:598
作者
Geijsen, N
Horoschak, M
Kim, K
Gribnau, J
Eggan, K
Daley, GQ
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] Massachusetts Gen Hosp, Ctr Regenerat Med & Technol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Childrens Hosp, Div Pediat Hematol Oncol, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Boston, MA 02115 USA
[6] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1038/nature02247
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Egg and sperm cells ( gametes) of the mouse are derived from a founder population of primordial germ cells that are set aside early in embryogenesis. Primordial germ cells arise from the proximal epiblast, a region of the early mouse embryo that also contributes to the first blood lineages of the embryonic yolk sac(1). Embryonic stem cells differentiate in vitro into cystic structures called embryoid bodies consisting of tissue lineages typical of the early mouse embryo(2,3). Because embryoid bodies sustain blood development, we reasoned that they might also support primordial germ cell formation. Here we isolate primordial germ cells from embryoid bodies, and derive continuously growing lines of embryonic germ cells. Embryonic germ cells show erasure of the methylation markers ( imprints) of the Igf2r and H19 genes, a property characteristic of the germlineage. We show that embryoid bodies support maturation of the primordial germ cells into haploid male gametes, which when injected into oocytes restore the somatic diploid chromosome complement and develop into blastocysts. Our ability to derive germ cells from embryonic stem cells provides an accessible in vitro model system for studies of germline epigenetic modification and mammalian gametogenesis.
引用
收藏
页码:148 / 154
页数:7
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