Dysmorphogenesis of lymph nodes in Foxc2 haploinsufficient mice

Histochem Cell Biol. 2011 Jun;135(6):603-13. doi: 10.1007/s00418-011-0819-x. Epub 2011 May 26.

Abstract

Dysmorphogenesis of lymph nodes displayed in a fork head transcription factor Foxc2 haploinsufficient mice--a model for lymphedema-distichiasis syndrome--was studied by immunohistochemistry and electron microscopy. The Foxc2 heterozygous mice manifested lymph node hyperplasia composed of conspicuous proliferation of endothelial cells forming the lymphatic sinus and α-smooth muscle actin (SMA)-immunopositive fibroblast-like cells in the lymphatic pulp, particularly around the sinus. The hyperplastic sinus endothelial cells and the SMA-positive cells demonstrated distinct immunolocalization of platelet-derived growth factor (PDGF)-B, a crucial chemoattractant for vascular mural cell recruitment, and its receptor, PDGFR-β, respectively. The observations suggest that the sinus endothelial cells elicit abnormal recruitment of the fibroblast-like cells as a type of vascular mural cells via PDGF-B/PDGFR-β signaling in lymph nodes of the Foxc2 heterozygotes. Furthermore, in Foxc2 heterozygous lymph nodes, recruited SMA-positive cells displayed an intense immunoreaction for vascular endothelial growth factor (VEGF)-C, a highly specific lymphangiogenic factor, and its receptor, VEGFR-3, was preferentially distributed in the lymphatic sinus endothelial cells. These findings suggest that an interactive cycle between lymphatic sinus endothelial cells and the fibroblast-like cells, which involves PDGF-B/PDGFR-β and VEGF-C/VEGFR-3 signaling, is essential for aberrant hyperplasia of the lymphatic sinus and the fibroblast-like cells in Foxc2 haploinsufficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Forkhead Transcription Factors / genetics*
  • Forkhead Transcription Factors / metabolism
  • Haploinsufficiency*
  • Hyperplasia / metabolism
  • Hyperplasia / pathology
  • Lymph Nodes / metabolism
  • Lymph Nodes / pathology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Platelet-Derived Growth Factor / metabolism
  • Receptor, Platelet-Derived Growth Factor beta / metabolism
  • Vascular Endothelial Growth Factor C / genetics
  • Vascular Endothelial Growth Factor C / metabolism

Substances

  • Forkhead Transcription Factors
  • Platelet-Derived Growth Factor
  • Vascular Endothelial Growth Factor C
  • mesenchyme fork head 1 protein
  • Receptor, Platelet-Derived Growth Factor beta