Graft cytokine mRNA activity in rat single lung transplants by reverse transcription-polymerase chain reaction: effect of cyclosporine

J Heart Lung Transplant. 1992 Nov-Dec;11(6):1041-5.

Abstract

Intragraft levels of cytokine mRNA were studied in an orthotopic rat left lung transplant model. Three groups of rats were compared at 7 days after transplantation. Isogeneic (Lewis to Lewis), allogeneic (Brown-Norway to Lewis) untreated, and cyclosporine-treated (25 mg/kg/day, intramuscularly) allogeneic animals underwent analysis of cytokine mRNA isolated from total RNA in freshly excised grafts. Reverse transcription-polymerase chain reaction amplification of interleukin (IL)-2, IL-4, and actin (control) mRNA was performed with custom-synthesized oligonucleotide amplimers targeted to known sequences of rat IL-2 and IL-4 cDNA. Semiquantitative analysis was performed by radioanalytic scanning of gel preparations. Sample specimens from the retrieved grafts were also graded histologically for rejection on a five-point scale. Rejection was most severe in the untreated allografts (p < 0.003). IL-2 mRNA was significantly greater in the untreated allografts when compared with isografts (p < 0.05) and cyclosporine-treated allografts (p < 0.05). No significant differences in IL-4 mRNA between groups were observed. We conclude that semiquantitative analysis of cytokine mRNA by reverse transcription-polymerase chain reaction is a useful and sensitive method for the study of acute rejection in lung grafts and that this technique may become an important tool in future studies of cytokine-mediated responses in cyclosporine-treated allografts.

Publication types

  • Comparative Study

MeSH terms

  • Actins / genetics*
  • Animals
  • Cyclosporine / therapeutic use*
  • Graft Rejection / diagnosis
  • Graft Rejection / genetics*
  • Immunosuppression Therapy
  • Interleukin-2 / genetics*
  • Interleukin-4 / genetics*
  • Lung Transplantation / immunology*
  • Male
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Inbred BN
  • Rats, Inbred Lew
  • Time Factors
  • Transcription, Genetic

Substances

  • Actins
  • Interleukin-2
  • RNA, Messenger
  • Interleukin-4
  • Cyclosporine