Protection against Fas-induced liver apoptosis in transgenic mice expressing cyclooxygenase 2 in hepatocytes

Hepatology. 2007 Mar;45(3):631-8. doi: 10.1002/hep.21556.

Abstract

Cyclooxygenase-2 (COX-2) is upregulated in many cancers, and the prostanoids synthesized increase proliferation, improve angiogenesis, and inhibit apoptosis in several tissues. To explore the function of COX-2 in liver, transgenic (Tg) mice were generated containing a fusion gene (LIVhCOX-2) consisting of human COX-2 cDNA under the control of the human ApoE promoter. Six lines were developed; all of them expressed the LIVhCOX-2 transgene selectively in hepatocytes. The Tg mice exhibited a normal phenotype, and the increased levels of PGE2 found were due to the constitutively expressed COX-2. Histological analysis of different tissues and macroscopic examination of the liver showed no differences between wild-type (Wt) and Tg animals. However, Tg animals were resistant to Fas-mediated liver injury, as demonstrated by low levels of plasmatic aminotransferases, a lesser caspase-3 activation, and Bax levels and an increase in Bcl-2, Mcl-1, and xIAP proteins, when compared with the Wt animals. Moreover, the resistance to Fas-mediated apoptosis is suppressed in the presence of COX-2-selective inhibitors, which prevented prostaglandin accumulation in the liver of Tg mice.

Conclusion: These results demonstrate that expression of COX-2-dependent prostaglandins exerted a protection against liver apoptosis.

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antibodies / pharmacology
  • Apoptosis / drug effects
  • Apoptosis / physiology*
  • Aspartate Aminotransferases / blood
  • Caspases / metabolism
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism*
  • Dinoprostone / metabolism
  • Gene Expression Regulation, Enzymologic
  • Hepatocytes / enzymology*
  • Humans
  • Liver / enzymology
  • Liver / pathology*
  • Mice
  • Mice, Transgenic
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • X-Linked Inhibitor of Apoptosis Protein / metabolism
  • fas Receptor / immunology
  • fas Receptor / physiology*

Substances

  • Antibodies
  • Fas protein, mouse
  • Mcl1 protein, mouse
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • X-Linked Inhibitor of Apoptosis Protein
  • fas Receptor
  • Cyclooxygenase 2
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Caspases
  • Dinoprostone