Fzd3 and Fzd6 deficiency results in a severe midbrain morphogenesis defect

Dev Dyn. 2010 Jan;239(1):246-60. doi: 10.1002/dvdy.22127.

Abstract

Wnt/beta-catenin signaling controls the proper development of the mid-/hindbrain region (MHR) and of midbrain dopaminergic (mDA) neurons, but the Frizzled (Fzd) receptors transducing these signals are still unknown. Fzd3 is expressed throughout the mouse anterior neural tube, whereas Fzd6 is restricted to the MHR. We show that the MHR is properly established and mDA neurons develop normally in Fzd6(-/-) mutants, but the number of mDA neurons is initially reduced and recovers at later stages in Fzd3(-/-) embryos. Fzd3(-/-); Fzd6(-/-) double mutants exhibit a severe midbrain morphogenesis defect consisting of collapsed brain ventricles, apparent thickening of the neuroepithelium, focal disruption of the ventricular basal lamina and protrusion of individual cells, and increased proliferation at later stages, despite a normal closure of the anterior neural tube and the rescue of the mDA defect in these embryos. Fzd3 and Fzd6 thus control proper midbrain morphogenesis by a yet unknown mechanism in the mouse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Bromodeoxyuridine
  • Frizzled Receptors / deficiency*
  • Frizzled Receptors / genetics
  • Gene Dosage / genetics
  • Immunohistochemistry
  • In Situ Hybridization
  • Mesencephalon / abnormalities*
  • Mesencephalon / embryology*
  • Mice
  • Mice, Knockout
  • Morphogenesis / genetics*
  • Receptors, G-Protein-Coupled / deficiency*
  • Receptors, G-Protein-Coupled / genetics

Substances

  • Frizzled Receptors
  • Fzd3 protein, mouse
  • Fzd6 protein, mouse
  • Receptors, G-Protein-Coupled
  • Bromodeoxyuridine