Understanding the Molecular Circuitry of Cell Lineage Specification in the Early Mouse Embryo

Genes

Anna Bergsmedh²  Mary E. Donohoe¹  Rebecca-Ayme Hughes¹ 

[1] Burke Medical Research Institute, White Plains, NY 10605, USA; E-Mail:;Center for Reproductive Medicine and Infertility, Weill Cornell Medical College, New York, NY 10065, USA; E-Mail:

关键词: mouse embryo;    early development;    lineage specification;    epigenetic marks;    transcriptional circuitry;    stem cells;   

DOI  :  10.3390/genes2030420

来源: mdpi

【 摘 要 】

Pluripotent stem cells hold great promise for cell-based therapies in regenerative medicine. However, critical to understanding and exploiting mechanisms of cell lineage specification, epigenetic reprogramming, and the optimal environment for maintaining and differentiating pluripotent stem cells is a fundamental knowledge of how these events occur in normal embryogenesis. The early mouse embryo has provided an excellent model to interrogate events crucial in cell lineage commitment and plasticity, as well as for embryo-derived lineage-specific stem cells and induced pluripotent stem (iPS) cells. Here we provide an overview of cell lineage specification in the early (preimplantation) mouse embryo focusing on the transcriptional circuitry and epigenetic marks necessary for successive differentiation events leading to the formation of the blastocyst.

【 授权许可】

CC BY   
© 2011 by the authors; licensee MDPI, Basel, Switzerland.