Macrophage cytotoxicity against murine meth A sarcoma involves nitric oxide-mediated apoptosis

Biochem Biophys Res Commun. 1996 Jun 25;223(3):643-9. doi: 10.1006/bbrc.1996.0948.

Abstract

We have studied the cytotoxic effect of stimulated macrophages on Meth A tumor cells in vitro. When stimulated with interferon-gamma and soluble beta-1,3-D-glucan, macrophages exerted cytotoxicity towards syngeneic Meth A tumor cells. This cytotoxicity was associated with a high level of nitric oxide production. Both cell death and nitric oxide production were significantly inhibited by the addition of aminoguanidine, a specific inhibitor of inducible nitric oxide synthase (iNOS), to the culture medium. The cytotoxic effect was accompanied by internucleosomal cleavage of DNA as shown by electrophoresis and DNA fragmentation assay.

MeSH terms

  • Animals
  • Apoptosis*
  • Cells, Cultured
  • Coculture Techniques
  • Female
  • Glucans / pharmacology*
  • Guanidines / pharmacology
  • Interferon Inducers / pharmacology*
  • Interferon-gamma / pharmacology*
  • Macrophage Activation* / drug effects
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Microscopy, Electron
  • Microscopy, Electron, Scanning
  • Nitric Oxide / physiology*
  • Nitrites / metabolism
  • Nitroprusside / pharmacology*
  • Recombinant Proteins
  • Sarcoma, Experimental / immunology*
  • Sarcoma, Experimental / pathology
  • Sarcoma, Experimental / ultrastructure
  • Tumor Cells, Cultured
  • beta-Glucans*

Substances

  • Glucans
  • Guanidines
  • Interferon Inducers
  • Nitrites
  • Recombinant Proteins
  • beta-Glucans
  • Nitroprusside
  • Nitric Oxide
  • Interferon-gamma
  • beta-1,3-glucan
  • pimagedine