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Copyright ©The Author(s) 2015.
World J Stem Cells. Apr 26, 2015; 7(3): 649-656
Published online Apr 26, 2015. doi: 10.4252/wjsc.v7.i3.649
Figure 1
Figure 1 First two cell segregations during preimplatation embryonic development. A: In blue, cells from the inner cell mass (ICM) in the early blastocyst, and white, cells from the trophectoderm; B: At the late blastocyst stage, cells from the ICM segregate into cells from the epiblast (green) and the primitive endoderm (orange).
Figure 2
Figure 2 Maintenance of pluripotency by leukemia inhibitory factor and small molecules. Green arrows indicate activation, red blunted lines indicate inhibition. The pluripotent cell must self-renew without committing to any specific cell type. This may be achieved by promoting self-renewal and inhibiting commitment by LIF; or by small molecules (in italic) which inhibit (1) signaling through the FGF receptor tyrosine kinase, thus inhibiting commitment; and (2) GSK3, promoting self-renewal. Adapted from[33]. LIF: Leukemia inhibitory factor; FGFr: Fibroblast growth factor receptor-specific tyrosine kinase; GSK3: Glycogen synthase kinase 3; MEK: Mitogen-activated protein kinase.