Tubulitis and epithelial cell alterations in mouse kidney transplant rejection are independent of CD103, perforin or granzymes A/B

Am J Transplant. 2006 Sep;6(9):2109-20. doi: 10.1111/j.1600-6143.2006.01483.x. Epub 2006 Jul 26.

Abstract

One of the defining lesions of kidney allograft rejection is epithelial deterioration and invasion by inflammatory cells (tubulitis). We examined epithelial changes and their relationship to effector T cells and to CD103/E-cadherin interactions in mouse kidney allografts. Rejecting allografts showed interstitial mononuclear infiltration from day 5. Loss of epithelial mass, estimated by tubular surface area, and tubulitis were minimal through day 7 and severe by day 21. Tubules in day 21 allografts manifested severe reduction of E-cadherin and Ksp-cadherin by immunostaining with redistribution to the apical membrane, indicating loss of polarity. By flow cytometry T cells isolated from allografts were 25% CD103+. Laser capture microdissection and RT-PCR showed increased CD103 mRNA in the interstitium and tubules. However, allografts in hosts lacking CD103 developed tubulitis, cadherin loss, and epithelial deterioration similar to wild-type hosts. The loss of cadherins and epithelial mass was also independent of perforin and granzymes A and B. Thus rejection is characterized by severe tubular deterioration associated with CD103+ T cells but not mediated by CD103/cadherin interactions or granzyme-perforin cytotoxic mechanisms. We suggest that alloimmune effector T cells mediate epithelial injury by contact-independent mechanisms related to delayed type hypersensitivity, followed by invasion of the altered epithelium to produce tubulitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / metabolism*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology*
  • Graft Rejection / metabolism
  • Graft Rejection / pathology*
  • Granzymes
  • Immunoenzyme Techniques
  • Integrin alpha Chains / genetics
  • Integrin alpha Chains / metabolism*
  • Kidney Transplantation*
  • Kidney Tubules / metabolism
  • Kidney Tubules / pathology*
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Knockout
  • Nephritis / metabolism
  • Nephritis / pathology*
  • Pore Forming Cytotoxic Proteins
  • Reverse Transcriptase Polymerase Chain Reaction
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism*
  • T-Lymphocytes / immunology
  • Transplantation, Homologous

Substances

  • Antigens, CD
  • Integrin alpha Chains
  • Membrane Proteins
  • Pore Forming Cytotoxic Proteins
  • alpha E integrins
  • perforin, mouse
  • Granzymes
  • Gzmb protein, mouse
  • Serine Endopeptidases