Direct neural fate specification from embryonic stem cells: a primitive mammalian neural stem cell stage acquired through a default mechanism

Neuron. 2001 Apr;30(1):65-78. doi: 10.1016/s0896-6273(01)00263-x.

Abstract

Little is known about how neural stem cells are formed initially during development. We investigated whether a default mechanism of neural specification could regulate acquisition of neural stem cell identity directly from embryonic stem (ES) cells. ES cells cultured in defined, low-density conditions readily acquire a neural identity. We characterize a novel primitive neural stem cell as a component of neural lineage specification that is negatively regulated by TGFbeta-related signaling. Primitive neural stem cells have distinct growth factor requirements, express neural precursor markers, generate neurons and glia in vitro, and have neural and non-neural lineage potential in vivo. These results are consistent with a default mechanism for neural fate specification and support a model whereby definitive neural stem cell formation is preceded by a primitive neural stem cell stage during neural lineage commitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning / drug effects
  • Body Patterning / physiology*
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Lineage / drug effects
  • Cell Lineage / physiology*
  • Cell Size / genetics
  • Cells, Cultured / cytology
  • Cells, Cultured / drug effects
  • Cells, Cultured / metabolism
  • Chimera / embryology
  • Chimera / genetics
  • Chimera / metabolism
  • Culture Media, Serum-Free / pharmacology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Growth Inhibitors / pharmacology
  • Growth Substances / deficiency
  • Interleukin-6*
  • Intermediate Filament Proteins / drug effects
  • Intermediate Filament Proteins / metabolism
  • Leukemia Inhibitory Factor
  • Lymphokines / pharmacology
  • Mammals / embryology*
  • Mammals / metabolism
  • Mice
  • Nerve Tissue Proteins*
  • Nervous System / cytology
  • Nervous System / embryology*
  • Nervous System / growth & development*
  • Nestin
  • Neurons / cytology*
  • Neurons / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Smad4 Protein
  • Stem Cells / cytology*
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transforming Growth Factor beta / drug effects
  • Transforming Growth Factor beta / metabolism

Substances

  • Culture Media, Serum-Free
  • DNA-Binding Proteins
  • Growth Inhibitors
  • Growth Substances
  • Interleukin-6
  • Intermediate Filament Proteins
  • Leukemia Inhibitory Factor
  • Lif protein, mouse
  • Lymphokines
  • Nerve Tissue Proteins
  • Nes protein, mouse
  • Nestin
  • Smad4 Protein
  • Smad4 protein, mouse
  • Trans-Activators
  • Transforming Growth Factor beta