Expression of GMP-140 (P-selectin) correlates with graft viability in cold-preserved rat livers

Transplantation. 2000 Jun 15;69(11):2440-2. doi: 10.1097/00007890-200006150-00039.

Abstract

Background: Ischemia/reperfusion injury is an inflammatory process involving cytokine release, Kupffer cell activation, and sinusoidal endothelial cell activation. GMP-140 is synthesized by endothelial cells.

Methods: We analyzed by Western blotting the expression of GMP-140 in a syngeneic rat liver transplantation model using grafts preserved for different periods of time.

Results: Compared with prereperfusion samples, expression did not change significantly in freshly harvested and 4-hr preserved livers. In grafts preserved for 24 hr (100% survival), GMP-140 levels increased dramatically at 1 hr, then returned to baseline at 24 hr after transplantation. Forty-eight hour preserved grafts (0% survival) showed a decreasing expression. To identify possible mediators, the effects of tumor necrosis factor-alpha and interleukin-1beta on GMP-140 expression in primary sinusoidal endothelial cells were analyzed. These cytokines increased both the percentage of stained cells as well as their mean staining fluorescence.

Conclusions: The absence of increase in 48-hr grafts suggests that GMP-140 may distinguish viable from nonviable livers.

MeSH terms

  • Animals
  • Cells, Cultured
  • Cryopreservation*
  • Graft Survival* / drug effects
  • In Vitro Techniques
  • Interleukin-1 / pharmacology
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism
  • Liver / physiopathology*
  • Liver Transplantation*
  • Male
  • P-Selectin / metabolism*
  • Rats
  • Rats, Inbred Lew
  • Thrombin / pharmacology
  • Tissue Distribution
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Interleukin-1
  • P-Selectin
  • Tumor Necrosis Factor-alpha
  • Thrombin