Beta-catenin signaling negatively regulates intermediate progenitor population numbers in the developing cortex

PLoS One. 2010 Aug 25;5(8):e12376. doi: 10.1371/journal.pone.0012376.

Abstract

Intermediate progenitor cells constitute a second proliferative cell type in the developing mammalian cerebral cortex. Little is known about the factors that govern the production of intermediate progenitors. Although persistent expression of stabilized beta-catenin was found to delay the maturation of radial glial progenitors into intermediate progenitors, the relationship between beta-catenin signaling and intermediate progenitors remains poorly understood. Using a transgenic reporter mouse for Axin2, a direct target of Wnt/beta-catenin signaling, we observed that beta-catenin signaling is decreased in intermediate progenitor cells relative to radial glial progenitors. Conditional deletion of beta-catenin from mouse cortical neural progenitors increased intermediate progenitor numbers, while conditional expression of stabilized beta-catenin reduced the intermediate progenitor population. Together, these findings provide evidence that beta-catenin signaling in radial progenitors negatively regulates intermediate progenitor cell number during cortical development.

Publication types

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

MeSH terms

  • Animals
  • Cell Count
  • Cerebral Cortex / cytology*
  • Cerebral Cortex / growth & development*
  • Cerebral Cortex / metabolism
  • Gene Expression Regulation
  • Mice
  • Molecular Imaging
  • Protein Stability
  • Signal Transduction*
  • Stem Cells / cytology*
  • Stem Cells / metabolism*
  • T-Box Domain Proteins / metabolism
  • beta Catenin / deficiency
  • beta Catenin / genetics
  • beta Catenin / metabolism*

Substances

  • Eomes protein, mouse
  • T-Box Domain Proteins
  • beta Catenin