Stimulation of hepatocyte survival and suppression of CCl4-induced liver injury by the adenovirally introduced C/EBPbeta gene

Biochem Biophys Res Commun. 2005 Apr 1;329(1):182-7. doi: 10.1016/j.bbrc.2005.01.113.

Abstract

Gene therapy has attracted attention as a potentially effective alternative to liver transplantation for the treatment of hepatic failure. We chose the C/EBPbeta gene, which plays vital roles in liver regeneration, as a candidate for gene therapy, and examined its effect on hepatocyte survival and the suppression of liver inflammation. C/EBPbeta gene overexpression significantly maintained hepatocyte viability during 12 days of the culture. Urea synthesis ability, which is a liver-specific function, in Adv-C/EBPbeta-infected hepatocytes was stably maintained during the culture, but the activity per cell was significantly lower than that in non-infected cells. On the contrary, DNA synthesis activity in Adv-C/EBPbeta-infected hepatocytes was significantly higher than that in non-infected cells. COX-2 was induced in Adv-C/EBPbeta-infected hepatocytes, and the addition of NS398, a specific inhibitor of COX-2, suppressed the viability-maintenance effect. COX-2 was thus shown to be involved in the survival effect of C/EBPbeta gene. The introduction of the C/EBPbeta gene into liver-damaged mice significantly suppressed the serum AST and ALT activities. These results indicate that C/EBPbeta appears to be a survival factor under stressful conditions, and the introduction of the gene has therapeutic function against liver injury.

MeSH terms

  • Adenoviridae / genetics
  • Adenoviridae / metabolism
  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Bromodeoxyuridine / pharmacology
  • CCAAT-Enhancer-Binding Protein-beta / genetics
  • Carbon Tetrachloride / pharmacology
  • Cell Nucleus / metabolism
  • Cell Survival
  • Cells, Cultured
  • Culture Media / pharmacology
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / pharmacology
  • DNA / metabolism
  • Genetic Therapy / methods
  • Genetic Vectors
  • Hepatocytes / cytology*
  • Hepatocytes / metabolism
  • Inflammation
  • Lac Operon
  • Liver / injuries*
  • Liver / metabolism
  • Liver / pathology
  • Mice
  • Mice, Inbred BALB C
  • Nitrobenzenes / pharmacology
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sulfonamides / pharmacology
  • Temperature
  • Time Factors
  • Urea / metabolism

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • Culture Media
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Nitrobenzenes
  • Sulfonamides
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide
  • Urea
  • DNA
  • Carbon Tetrachloride
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Bromodeoxyuridine