Renal tubular dysgenesis and tubulointerstitial nephritis antigen in juvenile nephronophthisis

Nephrology (Carlton). 2011 Jul;16(5):495-501. doi: 10.1111/j.1440-1797.2011.01442.x.

Abstract

Aim: The relationship between abnormalities of tubular architecture and tubulointerstitial nephritis antigen (TIN-ag) in juvenile nephronophthisis (J-NPH) was evaluated.

Methods: Sixteen J-NPH patients were examined. Nephrocystin-1, TIN-ag, type IV collagen, Fas antigen and the C5b-9 complement complex were stained by immunohistochemical methods.

Results: Renal tubules of patients with J-NPH showed morphological abnormalities of tubular basement membranes (TBM) and frequent apoptosis of tubular epithelial cells. Additionally, the C5b-9 complement complex was deposited within the TBM in the absence of immunoglobulin deposition, suggesting complement-dependent TBM injury. Localization of TIN-ag in the TBM of J-NPH patients disclosed a partial defect or discontinuity in 14 of the 16 patients, while type IV collagen immunoreactivity was relatively preserved. These findings suggest that tubulogenesis is disturbed during nephronogenesis in J-NPH patients because of a defect in nephrocystin, an NPHP gene product. TBM defects induce further morphological abnormalities such as cystic dilation of tubules; as tubular function impairment advances, the incomplete tubules may be injured by C5b-9 complement complexes, followed by apoptotic cell death.

Conclusion: TIN-ag, which is important in early nephrogenesis, lacks normal activity, and vulnerable and incomplete tubules with deficient TIN-ag expression are formed. Removal of these defective tubules by apoptosis combined with the C5b-9 complement complex could be the primary reason for progression to end-stage renal disease in J-NPH patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basement Membrane / pathology
  • Cell Adhesion Molecules / analysis
  • Cell Adhesion Molecules / physiology*
  • Collagen Type IV / analysis
  • Complement Membrane Attack Complex / analysis
  • Humans
  • Kidney Diseases, Cystic / complications
  • Kidney Diseases, Cystic / congenital*
  • Kidney Failure, Chronic / etiology*
  • Kidney Tubules / abnormalities*
  • fas Receptor / analysis

Substances

  • Cell Adhesion Molecules
  • Collagen Type IV
  • Complement Membrane Attack Complex
  • TINAG protein, human
  • fas Receptor

Supplementary concepts

  • Nephronophthisis, familial juvenile