Cited from the paper "Nanog Is the Gateway to the Pluripotent Ground State"
" After fertilization, mammalian zygotes follow a program of cleavage
divisions and elaborate two extraembryonic lineages, trophoblast and
hypoblast (Selwood and Johnson, 2006).
This preparatory phase of development culminates in creation of the
embryo founder tissue, a population of unrestricted pluripotent cells
known as the epiblast (Gardner and Beddington, 1988 and Nichols and Smith, 2009).
The epiblast proliferates to provide the substrate for axis formation,
germlayer specification, and gastrulation. Naive early epiblast cells
can be immortalized in culture in the form of embryonic stem (ES) cells (Brook and Gardner, 1997, Evans and Kaufman, 1981 and Martin, 1981).
Pluripotent cells can also be created outside the embryo by
reprogramming somatic cells, either by fusion with pre-existing
pluripotent cells (Miller and Ruddle, 1976, Tada et al., 1997, Tada et al., 2001 and Takagi et al., 1983) or, more compellingly, by transfection with regulatory transcription factors (Takahashi and Yamanaka, 2006)."
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Cited from the paper "Control of ground-state pluripotency by allelic regulation of Nanog"
"The ICM (inner cell mass) of the late blastocyst contains two lineages: the
extra-embryonic primitive endoderm, and the ‘ground-state’ pluripotent
epiblast6, 8, which gives rise to the embryo. Inner cells expressing Nanog biallelically also express Oct4 but not Gata4, a primitive endoderm marker9, and therefore are epiblast cells."
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