Defining pathways that enforce cell lineage specification in early development and stem cells

被引:24
作者
Roper, Stephen [1 ]
Hemberger, Myriam [1 ]
机构
[1] Babraham Inst, Lab Dev Genet & Imprinting, Cambridge CB22 3AT, England
基金
英国医学研究理事会;
关键词
blastocyst; cell fate; development; early embryo; lineage commitment; pluripotency; stem cells; transdifferentiation; trophoblast; EARLY MOUSE DEVELOPMENT; HELIX TRANSCRIPTION FACTOR; TISSUE-SPECIFIC EXPRESSION; EMBRYONAL CARCINOMA-CELLS; TROPHOBLAST GIANT-CELLS; RECEPTOR ERR-BETA; SELF-RENEWAL; IN-VITRO; PLACENTAL DEVELOPMENT; MAMMALIAN DEVELOPMENT;
D O I
10.4161/cc.8.10.8381
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The molecular processes that govern the first cell lineage decisions after fertilization also dictate the developmental potency of stem cells derived from the early mouse embryo. Our understanding of these mechanisms is therefore instrumental for stem cell biology and regenerative medicine. A number of transcription factors are known that determine a cell's fate towards either the embryonic or extraembryonic trophoblast lineages. Recent insights have shown that the definitive fixation of cell lineage fate is achieved by an epigenetic restriction through DNA methylation of the transcription factor Elf5. Lineage crossover can be induced, however, by manipulation of lineage determinants and gatekeepers, or their epigenetic regulation. Here we summarize the accumulating number of experimental conditions where such 'transdifferentiation' is observed that shed light onto the genetic and epigenetic pathways involved in lineage separation and the developmental potential of stem cells.
引用
收藏
页码:1515 / 1525
页数:11
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