The cerebrospinal fluid provides a proliferative niche for neural progenitor cells

Neuron. 2011 Mar 10;69(5):893-905. doi: 10.1016/j.neuron.2011.01.023.

Abstract

Cortical development depends on the active integration of cell-autonomous and extrinsic cues, but the coordination of these processes is poorly understood. Here, we show that the apical complex protein Pals1 and Pten have opposing roles in localizing the Igf1R to the apical, ventricular domain of cerebral cortical progenitor cells. We found that the cerebrospinal fluid (CSF), which contacts this apical domain, has an age-dependent effect on proliferation, much of which is attributable to Igf2, but that CSF contains other signaling activities as well. CSF samples from patients with glioblastoma multiforme show elevated Igf2 and stimulate stem cell proliferation in an Igf2-dependent manner. Together, our findings demonstrate that the apical complex couples intrinsic and extrinsic signaling, enabling progenitors to sense and respond appropriately to diffusible CSF-borne signals distributed widely throughout the brain. The temporal control of CSF composition may have critical relevance to normal development and neuropathological conditions.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Animals
  • Brain Neoplasms / cerebrospinal fluid
  • Cell Proliferation
  • Cerebral Cortex / cytology
  • Cerebral Cortex / physiology*
  • Cerebrospinal Fluid / physiology*
  • Glioblastoma / cerebrospinal fluid
  • Humans
  • Insulin-Like Growth Factor II / metabolism
  • Membrane Proteins / metabolism
  • Mice
  • Neural Stem Cells / cytology
  • Neural Stem Cells / physiology*
  • Neurons / metabolism
  • Nucleoside-Phosphate Kinase / metabolism
  • PTEN Phosphohydrolase / metabolism
  • Receptor, IGF Type 1 / metabolism
  • Statistics, Nonparametric

Substances

  • Membrane Proteins
  • Insulin-Like Growth Factor II
  • Receptor, IGF Type 1
  • Nucleoside-Phosphate Kinase
  • Mpp5 protein, mouse
  • PTEN Phosphohydrolase