Expression of osteopontin mRNA in normal and stone-forming rat kidney

Urol Res. 1998;26(6):389-94. doi: 10.1007/s002400050074.

Abstract

Human urine contains several macromolecules which inhibit calcium oxalate crystallization. Osteopontin (or uropontin), a secreted phosphoglycoprotein with the amino acid sequence Arg-Gly-Asp (RGD) and high affinity to hydroxyapatite, is one such inhibitor. To investigate the action of this protein on renal stone formation, the expression osteopontin gene in normal and chemically induced urolithiasis rat kidney was compared at both mRNA and protein levels. Northern blot analysis shown a significant increase of osteopontin mRNA level in stone-forming rat kidney compared with normal ones. In an in situ hybridization study, we localized the transcripts of the osteopontin gene in epithelial cells of both distal and collective tubules, and found a remarkably strong signal in stone-forming rats. The amount and distribution of the protein in kidney from immunocytochemistry staining showed the same pattern as seen in situ hybridization. These findings indicate that osteopontin may be an important macromolecule in the normal endogenous defence against the formation of urinary calculi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Calcium Oxalate / analysis
  • Gene Expression
  • Immunoenzyme Techniques
  • In Situ Hybridization
  • Kidney Calculi / chemistry*
  • Kidney Calculi / physiopathology*
  • Male
  • Microscopy, Polarization
  • Osteopontin
  • Phosphoproteins / analysis
  • Phosphoproteins / genetics
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Sialoglycoproteins / analysis
  • Sialoglycoproteins / genetics*

Substances

  • Phosphoproteins
  • RNA, Messenger
  • SPP1 protein, human
  • Sialoglycoproteins
  • Spp1 protein, rat
  • Osteopontin
  • Calcium Oxalate