TY - JOUR
T1 - Dynamic Equilibrium and Heterogeneity of Mouse Pluripotent Stem Cells with Distinct Functional and Epigenetic States
AU - Hayashi, Katsuhiko
AU - Lopes, Susana M.Chuva de Sousa
AU - Tang, Fuchou
AU - Surani, M. Azim
N1 - Funding Information:
We are grateful to T. Nakano for anti-PGC7 and P. Beverly for mouse anti-SSEA1. We thank C. Lee for technical support; C. Mummery for continuing support; and A. McLaren, B. Payer, P. Hajkova, and S. Jeffries for useful comments on the manuscript. This work was supported by the Netherlands Organization for Scientific Research (NWO, TALENT 809.67.024) to S.M.C.S.L.; the Japan Society for Promotion of Science to K.H.; and The Technology Programme (DTI Project Number TP/4/BIO/6/I/22020) of CellCentric Ltd and The Technology Strategy Board sponsored by the Department for Innovation, Universities, and Skills (DIUS); and the Wellcome Trust (062801).
PY - 2008/10/9
Y1 - 2008/10/9
N2 - Embryonic stem cells (ESCs) are apparently homogeneous self-renewing cells, but we observed heterogeneous expression of Stella in ESCs, which is a marker of pluripotency and germ cells. Here we show that, whereas Stella-positive ESCs were like the inner cell mass (ICM), Stella-negative cells were like the epiblast cells. These states were interchangeable, which reflects the metastability and plasticity of ESCs. The established equilibrium was skewed reversibly in the absence of signals from feeder cells, which caused a marked shift toward an epiblast-like state, while trichostatin A, an inhibitor of histone deactelylase, restored Stella-positive population. The two populations also showed different histone modifications and striking functional differences, as judged by their potential for differentiation. The Stella-negative ESCs were more like the postimplantation epiblast-derived stem cells (EpiSCs), albeit the stella locus was repressed by DNA methylation in the latter, which signifies a robust epigenetic boundary between ESCs and EpiSCs.
AB - Embryonic stem cells (ESCs) are apparently homogeneous self-renewing cells, but we observed heterogeneous expression of Stella in ESCs, which is a marker of pluripotency and germ cells. Here we show that, whereas Stella-positive ESCs were like the inner cell mass (ICM), Stella-negative cells were like the epiblast cells. These states were interchangeable, which reflects the metastability and plasticity of ESCs. The established equilibrium was skewed reversibly in the absence of signals from feeder cells, which caused a marked shift toward an epiblast-like state, while trichostatin A, an inhibitor of histone deactelylase, restored Stella-positive population. The two populations also showed different histone modifications and striking functional differences, as judged by their potential for differentiation. The Stella-negative ESCs were more like the postimplantation epiblast-derived stem cells (EpiSCs), albeit the stella locus was repressed by DNA methylation in the latter, which signifies a robust epigenetic boundary between ESCs and EpiSCs.
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U2 - 10.1016/j.stem.2008.07.027
DO - 10.1016/j.stem.2008.07.027
M3 - Article
C2 - 18940731
AN - SCOPUS:53049092465
SN - 1934-5909
VL - 3
SP - 391
EP - 401
JO - Cell stem cell
JF - Cell stem cell
IS - 4
ER -