Gene silencing of 4-1BB by RNA interference inhibits acute rejection in rats with liver transplantation

Biomed Res Int. 2013:2013:192738. doi: 10.1155/2013/192738. Epub 2013 Jan 31.

Abstract

The 4-1BB signal pathway plays a key role in organ transplantation tolerance. In this study, we have investigated the effect of gene silencing of 4-1BB by RNA interference (RNAi) on the acute rejection in rats with liver transplantation. The recombination vector of lentivirus that contains shRNA targeting the 4-1BB gene (LV-sh4-1BB) was constructed. The liver transplantation was performed using the two-cuff technique. Brown-Norway (BN) recipient rats were infected by the recombinant LVs. The results showed that gene silencing of 4-1BB by RNAi downregulated the 4-1BB gene expression of the splenic lymphocytes in vitro, and the splenic lymphocytes isolated from the rats with liver transplantation. LV-sh4-1BB decreased the plasma levels of liver injury markers including AST, ALT, and BIL and also decreased the level of plasma IL-2 and IFN- γ in recipient rats with liver transplantation. Lentivirus-mediated delivery of shRNA targeting 4-1BB gene prolonged the survival time of recipient and alleviated the injury of liver morphology in recipient rats with liver transplantation. In conclusion, our results demonstrate that gene silencing of 4-1BB by RNA interference inhibits the acute rejection in rats with liver transplantation.

MeSH terms

  • Animals
  • Cell Line
  • Graft Rejection / genetics
  • Graft Rejection / immunology
  • Graft Rejection / metabolism*
  • Graft Rejection / pathology
  • Graft Rejection / prevention & control
  • Humans
  • Lentivirus
  • Liver Transplantation*
  • Lymphocytes / immunology
  • Lymphocytes / metabolism
  • Lymphocytes / pathology
  • RNA Interference*
  • Rats
  • Spleen / immunology
  • Spleen / metabolism
  • Spleen / pathology
  • Transduction, Genetic
  • Transplantation, Homologous
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / genetics
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / immunology
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / metabolism*

Substances

  • Tumor Necrosis Factor Receptor Superfamily, Member 9