Vascular endothelial growth factor (VEGF-C1)-dependent inflammatory response of podocytes in nephrotic syndrome glomerulopathies in children: an immunohistochemical approach

Histopathology. 2005 Feb;46(2):176-83. doi: 10.1111/j.1365-2559.2005.02076.x.

Abstract

Aims: To analyse expression and distribution of vascular endothelial growth factor (VEGF-C1), podocalyxin and synaptopodin within renal tissue in nephrotic syndrome glomerulopathies in children.

Methods and results: Renal biopsies performed at the time and in the manner recommended by the World Health Organization. The study group consisted of submicroscopic glomerulonephritis (n = 10), diffuse mesangial proliferation (n = 14) and focal segmental glomerulosclerosis (n = 5). The control tissue consisted of macroscopically normal appearing cortex taken from kidneys resected for localized neoplasms (n = 3). Material for immunohistochemistry was fixed in Bouin's solution and embedded in paraffin. Indirect immunohistochemistry using monoclonal anti-human antibodies directed against VEGF-C1, podocalyxin and synaptopodin was employed. The distribution of markers was quantified by computerized image analysis. In non-sclerosed glomeruli (within podocyte cytoplasm), VEGF-C1 was more expressed in podocytes of all groups (P < 0.0002), while the distribution of synaptopodin was less expressed in all groups (P < 0.0002). There was no statistical difference between all groups in the expression of podocalyxin.

Conclusions: The increased permeability of the filtration barrier in steroid-resistant glomerulopathies may be a consequence of subcellular changes in podocytes resulting from decreased expression of synaptopodin. Moreover, impaired permeability of endothelium could be secondary to increased expression of podocyte-derived VEGF-C1.

Publication types

  • Comparative Study

MeSH terms

  • Analysis of Variance
  • Child
  • Humans
  • Immunohistochemistry
  • Inflammation / metabolism
  • Kidney Glomerulus / chemistry
  • Kidney Glomerulus / pathology*
  • Microfilament Proteins / analysis
  • Nephrotic Syndrome / metabolism
  • Nephrotic Syndrome / pathology*
  • Sialoglycoproteins / analysis
  • Vascular Endothelial Growth Factor C / analysis*

Substances

  • Microfilament Proteins
  • SYNPO protein, human
  • Sialoglycoproteins
  • Vascular Endothelial Growth Factor C
  • podocalyxin