Meninges control tangential migration of hem-derived Cajal-Retzius cells via CXCL12/CXCR4 signaling

Nat Neurosci. 2006 Oct;9(10):1284-93. doi: 10.1038/nn1764. Epub 2006 Sep 10.

Abstract

Cajal-Retzius cells are critical in the development of the cerebral cortex, but little is known about the mechanisms controlling their development. Three focal sources of Cajal-Retzius cells have been identified in mice-the cortical hem, the ventral pallium and the septum-from where they migrate tangentially to populate the cortical surface. Using a variety of tissue culture assays and in vivo manipulations, we demonstrate that the tangential migration of cortical hem-derived Cajal-Retzius cells is controlled by the meninges. We show that the meningeal membranes are a necessary and sufficient substrate for the tangential migration of Cajal-Retzius cells. We also show that the chemokine CXCL12 secreted by the meninges enhances the dispersion of Cajal-Retzius cells along the cortical surface, while retaining them within the marginal zone in a CXCR4-dependent manner. Thus, the meningeal membranes are fundamental in the development of Cajal-Retzius cells and, hence, in the normal development of the cerebral cortex.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzylamines
  • Calbindin 2
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / metabolism
  • Cell Movement / physiology*
  • Cells, Cultured
  • Cerebral Cortex / cytology*
  • Chemokine CXCL12
  • Chemokines, CXC / metabolism
  • Cyclams
  • Embryo, Mammalian
  • Epithelial Cells / physiology
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism
  • Fluorescent Antibody Technique / methods
  • Green Fluorescent Proteins / metabolism
  • Heterocyclic Compounds / pharmacology
  • In Situ Hybridization / methods
  • Indoles
  • Laminin / metabolism
  • Meninges / cytology
  • Meninges / physiology*
  • Mice
  • Mice, Inbred ICR
  • Mice, Transgenic
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurons* / drug effects
  • Neurons* / physiology
  • Organ Culture Techniques
  • Receptors, CXCR4 / deficiency
  • Receptors, CXCR4 / physiology*
  • Reelin Protein
  • S100 Calcium Binding Protein G / metabolism
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Signal Transduction / physiology*
  • Transplants

Substances

  • Benzylamines
  • Calbindin 2
  • Cell Adhesion Molecules, Neuronal
  • Chemokine CXCL12
  • Chemokines, CXC
  • Cxcl12 protein, mouse
  • Cyclams
  • Extracellular Matrix Proteins
  • Heterocyclic Compounds
  • Indoles
  • Laminin
  • Nerve Tissue Proteins
  • Receptors, CXCR4
  • Reelin Protein
  • S100 Calcium Binding Protein G
  • Green Fluorescent Proteins
  • DAPI
  • Serine Endopeptidases
  • plerixafor