Neural stem cells have considerable therapeutic potential because of their ability to generate defined neuronal cell types for use in drug screening studies or cell-based therapies for neurodegenerative diseases. In this study, we differentiate mouse embryonic stem cells to neural progenitors with an initial forebrain identity in a defined system that enables systematic manipulation to generate more caudal fates, including motoneurons. We demonstrate that the ability to pattern embryonic stem cell-derived neural progenitors is temporally restricted and show that the loss of responsiveness to morphogenetic cues correlates with constitutive expression of the basic helix-loop-helix transcription factors Olig2 and Mash1, epidermal growth factor receptor, and vimentin and parallels the onset of gliogenesis. We provide evidence for two temporal classes of embryonic stem cell-derived putative radial glia that coincide with a transition from neurogenesis to gliogenesis and a concomitant loss of regional identity. ©AlphaMed Press.
CITATION STYLE
Bouhon, I. A., Joannides, A., Kato, H., Chandran, S., & Allen, N. D. (2006). Embryonic Stem Cell‐Derived Neural Progenitors Display Temporal Restriction to Neural Patterning. STEM CELLS, 24(8), 1908–1913. https://doi.org/10.1634/stemcells.2006-0031
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