New cell lines from mouse epiblast share defining features with human embryonic stem cells

• Published in: Nature 2007-07, Vol.448 (7150), p.196-199
• Main Authors: McKay, Ronald D. G, Brook, Frances A, Mack, David L, Gardner, Richard L, Chenoweth, Josh G, Davies, Timothy J, Evans, Edward P, Tesar, Paul J
• Format: Article
• Language: English
• Subjects: Animal models in research; Animals; Biological and medical sciences; Biology; Cell Culture Techniques; Cell Differentiation; Cell differentiation, maturation, development, hematopoiesis; Cell Line; Cell lines; Cell physiology; Embryo Implantation; Embryonic stem cells; Embryonic Stem Cells - cytology; Embryonic Stem Cells - metabolism; Embryos; Fundamental and applied biological sciences. Psychology; Gene Expression; Human; Humanities and Social Sciences; Humans; Implantation; Integrity; letter; Mice; Molecular and cellular biology; multidisciplinary; Origins; Pluripotent Stem Cells - cytology; Pluripotent Stem Cells - metabolism; Rodents; Science; Science (multidisciplinary); Signal Transduction; Stem cells; Transcription Factors - metabolism
• ISSN: 0028-0836; 1476-4687; 1476-4679
• DOI: 10.1038/nature05972

The application of human embryonic stem (ES) cells in medicine and biology has an inherent reliance on understanding the starting cell population. Human ES cells differ from mouse ES cells and the specific embryonic origin of both cell types is unclear. Previous work suggested that mouse ES cells could only be obtained from the embryo before implantation in the uterus. Here we show that cell lines can be derived from the epiblast, a tissue of the post-implantation embryo that generates the embryo proper. These cells, which we refer to as EpiSCs (post-implantation epiblast-derived stem cells), express transcription factors known to regulate pluripotency, maintain their genomic integrity, and robustly differentiate into the major somatic cell types as well as primordial germ cells. The EpiSC lines are distinct from mouse ES cells in their epigenetic state and the signals controlling their differentiation. Furthermore, EpiSC and human ES cells share patterns of gene expression and signalling responses that normally function in the epiblast. These results show that epiblast cells can be maintained as stable cell lines and interrogated to understand how pluripotent cells generate distinct fates during early development.