Stem Cell Reports · 2014 · 107 citations · 39 references
Life SciencesDevelopmental BiologyMolecular BiologyDevelopmental NeuroscienceEpigeneticsMolecular NeuroscienceDevelopmental EpigeneticsEpigenetic Control Of DifferentiationEpigenetic Regulation In DevelopmentNeural DevelopmentNeural DifferentiationNotch SignalingChromatin-associated Protein InteractionsEpigenetic Regulation Of DifferentiationMicrorna Control Of DifferentiationNeural Cell DifferentiationNeural Progenitor DifferentiationNeural Stem Cell DifferentiationNeural Stem Cell EpigeneticsNotch Signaling In Differentiation
It is clear that neural differentiation from human pluripotent stem cells generates cells that are developmentally immature. Here, we show that the let-7 plays a functional role in the developmental decision making of human neural progenitors, controlling whether these cells make neurons or glia. Through gain- and loss-of-function studies on both tissue and pluripotent derived cells, our data show that let-7 specifically regulates decision making in this context by regulation of a key chromatin-associated protein, HMGA2. Furthermore, we provide evidence that the let-7/HMGA2 circuit acts on HES5, a NOTCH effector and well-established node that regulates fate decisions in the nervous system. These data link the let-7 circuit to NOTCH signaling and suggest that this interaction serves to regulate human developmental progression.
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Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells
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Hes1 and Hes5 as Notch effectors in mammalian neuronal differentiation
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