PLoS ONE · 2013 · 26 citations · 45 references
Life SciencesCell BiologyDevelopmental BiologyCell SignalingGene ExpressionStem Cell BiologyEmbryonic Stem CellsStem Cell DifferentiationStem Cell PhysiologyStem Cell ProliferationStem Cell TumorigenicityEmbryonic Stem Cell Self-renewalHuman Embryonic Stem CellsInduced Pluripotent Stem CellsMicrorna In Stem Cell RegulationStem Cell Gene RegulationStem Cell Growth Factor SignalingStemness RegulationXeno-free Culture
We report that a single growth factor, NM23-H1, enables serial passaging of both human ES and iPS cells in the absence of feeder cells, their conditioned media or bFGF in a fully defined xeno-free media on a novel defined, xeno-free surface. Stem cells cultured in this system show a gene expression pattern indicative of a more "naïve" state than stem cells grown in bFGF-based media. NM23-H1 and MUC1* growth factor receptor cooperate to control stem cell self-replication. By manipulating the multimerization state of NM23-H1, we override the stem cell's inherent programming that turns off pluripotency and trick the cells into continuously replicating as pluripotent stem cells. Dimeric NM23-H1 binds to and dimerizes the extra cellular domain of the MUC1* transmembrane receptor which stimulates growth and promotes pluripotency. Inhibition of the NM23-H1/MUC1* interaction accelerates differentiation and causes a spike in miR-145 expression which signals a cell's exit from pluripotency.
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Embryonic Stem Cell Lines Derived from Human Blastocysts
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