Olig2-regulated lineage-restricted pathway controls replication competence in neural stem cells and malignant glioma

Neuron. 2007 Feb 15;53(4):503-17. doi: 10.1016/j.neuron.2007.01.009.

Abstract

Recent studies have identified stem cells in brain cancer. However, their relationship to normal CNS progenitors, including dependence on common lineage-restricted pathways, is unclear. We observe expression of the CNS-restricted transcription factor, OLIG2, in human glioma stem and progenitor cells reminiscent of type C transit-amplifying cells in germinal zones of the adult brain. Olig2 function is required for proliferation of neural progenitors and for glioma formation in a genetically relevant murine model. Moreover, we show p21(WAF1/CIP1), a tumor suppressor and inhibitor of stem cell proliferation, is directly repressed by OLIG2 in neural progenitors and gliomas. Our findings identify an Olig2-regulated lineage-restricted pathway critical for proliferation of normal and tumorigenic CNS stem cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / deficiency
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Brain Neoplasms / pathology*
  • Bromodeoxyuridine / metabolism
  • Cell Differentiation / physiology
  • Cell Proliferation
  • Cells, Cultured
  • Chromatin Immunoprecipitation / methods
  • Cyclin-Dependent Kinase Inhibitor p16 / deficiency
  • Cyclin-Dependent Kinase Inhibitor p21 / genetics
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Embryo, Mammalian
  • Flow Cytometry
  • Glioma / pathology*
  • Green Fluorescent Proteins / biosynthesis
  • Luciferases / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, SCID
  • Mice, Transgenic
  • Nerve Tissue Proteins / deficiency
  • Nerve Tissue Proteins / metabolism*
  • Neurons / physiology*
  • Oligodendrocyte Transcription Factor 2
  • Stem Cells / physiology*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p16
  • Cyclin-Dependent Kinase Inhibitor p21
  • Nerve Tissue Proteins
  • Olig2 protein, mouse
  • Oligodendrocyte Transcription Factor 2
  • Green Fluorescent Proteins
  • Luciferases
  • Bromodeoxyuridine