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Transplant Proc ; 36(2): 353-5, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15050157

RESUMO

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.


Assuntos
Apoptose/fisiologia , Rejeição de Enxerto/patologia , Mucosa Intestinal/cirurgia , Intestino Delgado/cirurgia , Linfócitos/patologia , Transplante Homólogo/patologia , Transplante Isogênico/patologia , Animais , Proteína Ligante Fas , Mucosa Intestinal/patologia , Intestino Delgado/patologia , Linfócitos/fisiologia , Glicoproteínas de Membrana/análise , Ratos , Ratos Endogâmicos BN , Ratos Endogâmicos Lew , Receptor fas/análise
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