Nitric oxide is an important mediator of renal tubular epithelial cell death in vitro and in murine experimental hydronephrosis

Am J Pathol. 2006 Aug;169(2):388-99. doi: 10.2353/ajpath.2006.050964.

Abstract

Macrophages play a pivotal role in tissue injury and fibrosis during renal inflammation. Although macrophages may induce apoptosis of renal tubular epithelial cells, the mechanisms involved are unclear. We used a microscopically quantifiable co-culture assay to dissect the cytotoxic interaction between murine bone marrow-derived macrophages and Madin-Darby canine kidney cells and primary murine renal tubular epithelial cells. The induction of tubular cell apoptosis by cytokine-activated macrophages was reduced by inhibitors of nitric oxide synthase whereas tubular cell proliferation was unaffected. Furthermore, cytokine-activated macrophages derived from mice targeted for the deletion of inducible nitric oxide synthase were noncytotoxic. We then examined the role of nitric oxide in vivo by inhibiting inducible nitric oxide synthase in the model of murine experimental hydronephrosis. l-N(6)-(1-iminoethyl)-lysine was administered in the drinking water between days 5 and 7 after ureteric obstruction. Macrophage infiltration was comparable between groups, but treatment significantly inhibited tubular cell apoptosis at day 7. Tubular cell proliferation was unaffected. Inducible nitric oxide synthase blockade also reduced interstitial cell apoptosis and increased collagen III deposition. These data indicate that nitric oxide is a key mediator of macrophage-directed tubular cell apoptosis in vitro and in vivo and also modulates tubulointerstitial fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cytokines / immunology
  • Disease Models, Animal
  • Dogs
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / enzymology
  • Epithelial Cells / pathology*
  • Fibrosis / pathology
  • Hydronephrosis / chemically induced*
  • Kidney Tubules / cytology
  • Kidney Tubules / drug effects
  • Kidney Tubules / enzymology
  • Kidney Tubules / pathology*
  • Lysine / analogs & derivatives
  • Lysine / pharmacology
  • Macrophage Activation / drug effects
  • Macrophage Activation / immunology
  • Mice
  • Nephritis, Interstitial / pathology
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase Type II / antagonists & inhibitors

Substances

  • Cytokines
  • N(6)-(1-iminoethyl)lysine
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Lysine