beta-Catenin expression during vascular development and degeneration of avian mesonephros

J Anat. 2005 Feb;206(2):165-74. doi: 10.1111/j.1469-7580.2005.00382.x.

Abstract

beta-Catenin is a structural component of adherens junctions, a regulator of the Wnt signalling pathway and a transcriptional co-activator with a key role in vascular patterning. The avian mesonephros is a transitory embryonic kidney that is used in the study of vascular development and degeneration. Here we examine beta-catenin expression in this model during vascular development and degeneration. Quail embryos with developing or degenerating mesonephros were studied, on day 6 (30HH) or day 11 of incubation (40HH), respectively. QH1 whole mounts of developing mesonephros revealed numerous angioblast-like cells situated in the paramesonephric duct that seem to invade the mesonephros. Although these cells did not express beta-catenin, the surrounding periductal mesenchymal cells translocated high levels of beta-catenin into the nucleus. In contrast, degenerating mesonephros were devoid of angioblast-like cells and beta-catenin was lower than in the developing mesonephros. beta-Catenin was significantly reduced in the glomerular capillary tuffs, indicating that it was particularly down-regulated in the vascular system. No sex-related differences in beta-catenin expression were observed in degenerating mesonephros. Furthermore, two special populations of glomerular and peritubular endothelial cells were observed in degenerating mesonephros: one translocating beta-catenin into the nucleus and the other in apoptosis that did not translocate it. In conclusion, our results indicate that the paramesonephric duct is a potential new vasculogenetic pathway, and suggest that beta-catenin plays a role in the fate of mesonephric endothelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Biological Transport
  • Blood Vessels
  • Blotting, Western / methods
  • Cell Nucleus / metabolism
  • Cytoskeletal Proteins / analysis*
  • Cytoskeletal Proteins / metabolism
  • Endothelial Cells / metabolism
  • Female
  • Immunohistochemistry / methods
  • Male
  • Mesonephros / blood supply
  • Mesonephros / physiology*
  • Microscopy, Electron, Scanning
  • Quail / embryology*
  • Trans-Activators / analysis*
  • Trans-Activators / metabolism
  • beta Catenin

Substances

  • Cytoskeletal Proteins
  • Trans-Activators
  • beta Catenin