Detailed analysis of mucosal restoration of the small intestine after the cavitary two-layer cold storage method

Am J Transplant. 2005 Sep;5(9):2135-42. doi: 10.1111/j.1600-6143.2005.01001.x.

Abstract

Small bowel transplantation (SBT) is associated with a high incidence of infectious complications because of ischemia/reperfusion (I/R) mucosal injury concomitant with potent immunosuppression. In this study, we evaluated whether the cavitary two-layer method (cTLM) could reduce I/R injury and allow early mucosal restoration, particularly after prolonged preservation and transplantation. Canine heterotopic segmental SBT was performed immediately without preservation (group 1), after 24-h preservation in UW solution (group 2) or by the cTLM (group 3). The graft samples were taken 1 h after reperfusion and on days 1, 4 and 7. We assessed graft mucosa with detailed microscopic and electromicroscopic analyses. In Group 3, histological injury and cell apoptosis after transplantation were significantly alleviated and rapidly recovered to a similar level of group 1. The mucosal restoration was morphologically completed within 4 days. In contrast, in group 2, more pronounced mucosal injury and delayed recovery were noted. Crypt cell proliferation activity was well maintained in groups 1 and 3 throughout the experimental period. Our ultrastructural analysis suggested that mitochondrial integrity achieved by the cTLM was a basal mechanism under the prompt mucosal restoration. The cTLM could reduce I/R injury, facilitate mucosal regeneration and restore the nearly normal structure early after SBT.

MeSH terms

  • Animals
  • Apoptosis
  • Cell Proliferation
  • Cold Temperature
  • Dogs
  • Female
  • Graft Survival
  • Immunohistochemistry
  • Immunosuppressive Agents / pharmacology
  • In Situ Nick-End Labeling
  • Intestinal Mucosa / pathology*
  • Intestine, Small / pathology*
  • Male
  • Microscopy, Electron
  • Microscopy, Electron, Transmission
  • Mitochondria / pathology
  • Mucous Membrane / pathology
  • Organ Preservation / methods*
  • Organ Transplantation / methods*
  • Preservation, Biological
  • Proliferating Cell Nuclear Antigen / biosynthesis
  • Reperfusion
  • Reperfusion Injury / pathology
  • Time Factors

Substances

  • Immunosuppressive Agents
  • Proliferating Cell Nuclear Antigen