Regulation of neural stem/progenitor cell maintenance by PI3K and mTOR

Neurosci Lett. 2010 Feb 12;470(2):115-20. doi: 10.1016/j.neulet.2009.12.067. Epub 2010 Jan 1.

Abstract

Control of stem cell state and differentiation of neural stem/progenitor cells is essential for proper development of the nervous system. EGF and FGF2 play important roles in the control of neural stem/progenitor cells, but the underlying mechanism still remains unclear. Here we show, using in vitro primary cultures of mouse neural stem/progenitor cells, that both PI3K and mTOR are activated by EGF/FGF2 but that inhibiting the activation of either PI3K or mTOR alone results in only reduced proliferation of neural stem/progenitor cells without affecting their stem cell state, namely, the capacity to self-renew. However, significantly, concurrent inhibition of PI3K and mTOR promoted exit from the stem cell state together with astrocytic differentiation of neural stem/progenitor cells. These findings suggest that PI3K and mTOR are involved in the EGF/FGF2-mediated maintenance of neural stem/progenitor cells and that they may act in parallel and independent pathways, complementing and backing up each other to maintain the stem cell state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / physiology
  • Cell Differentiation / physiology
  • Cell Proliferation
  • Cells, Cultured
  • Epidermal Growth Factor / metabolism
  • Fibroblast Growth Factor 2 / metabolism
  • Glial Fibrillary Acidic Protein / metabolism
  • Intracellular Signaling Peptides and Proteins / antagonists & inhibitors
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Mice, Inbred Strains
  • Neurons / physiology*
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoinositide-3 Kinase Inhibitors
  • Prosencephalon / physiology
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / metabolism*
  • SOXB1 Transcription Factors / metabolism
  • Stem Cells / physiology*
  • TOR Serine-Threonine Kinases
  • Tubulin / metabolism

Substances

  • Glial Fibrillary Acidic Protein
  • Intracellular Signaling Peptides and Proteins
  • Phosphoinositide-3 Kinase Inhibitors
  • SOXB1 Transcription Factors
  • Sox2 protein, mouse
  • Tubulin
  • beta3 tubulin, mouse
  • Fibroblast Growth Factor 2
  • Epidermal Growth Factor
  • mTOR protein, mouse
  • Protein Serine-Threonine Kinases
  • TOR Serine-Threonine Kinases