Apoptosis of crypt cells and lymphocytes in gut-associated lymphoid tissues during small intestinal graft rejection in rats

Transplant Proc. 2004 Mar;36(2):353-5. doi: 10.1016/j.transproceed.2004.01.097.

Abstract

Introduction: We investigated the extent of apoptosis in crypt cells and Peyer's patches (PPs) during small bowel allograft rejection in rats to examine whether the Fas/FasL pathway participates in apoptosis within grafts during rejection.

Materials and methods: Orthotopic small bowel transplantation with portocaval drainage was performed from Brown Norway to Lewis (LEW) rats. Isografted (LEW --> LEW) and nontransplanted animals served as the controls. Animals were sacrificed on days 3, 5, on 7 after SBT (each n = 5). An in situ end-labeling (ISEL) technique was used to detect apoptotic cells. Indirect immunoperoxidase staining was also performed using monoclonal antibodies against rat Fas or Fas-L.

Results: The number of ISEL-positive enterocytes in the allografts increased significantly on days 3, 5, and 7. Similarly, in the PPs of the allografts, the number of ISEL-positive mononuclear cells increased significantly on days 3, 5, and 7. On day 7 the number of Fas- and FasL-positive enterocytes were increased significantly in the allografts compared with the nontransplanted controls. Similarly, in the PPs, Fas- and FasL-positive mononuclear cells also increased significantly on day 7 in the allograft.

Conclusion: Although an increase, number of apoptotic enterocytes and lymphocytes were observed in the early phase, activation of Fas/FasL system occurred during the late phase of small bowel graft rejection. These findings suggest that both rejection-associated and sepsis-induced forms of apoptosis may be associated with small bowel graft rejection.

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Fas Ligand Protein
  • Graft Rejection / pathology*
  • Intestinal Mucosa / pathology
  • Intestinal Mucosa / surgery*
  • Intestine, Small / pathology
  • Intestine, Small / surgery*
  • Lymphocytes / pathology*
  • Lymphocytes / physiology
  • Membrane Glycoproteins / analysis
  • Rats
  • Rats, Inbred BN
  • Rats, Inbred Lew
  • Transplantation, Homologous / pathology*
  • Transplantation, Isogeneic / pathology*
  • fas Receptor / analysis

Substances

  • Fas Ligand Protein
  • Faslg protein, rat
  • Membrane Glycoproteins
  • fas Receptor