Allograft rejection-related gene expression in the endothelial cells of renal transplantation recipients after cytomegalovirus infection

J Zhejiang Univ Sci B. 2009 Nov;10(11):820-8. doi: 10.1631/jzus.B0920115.

Abstract

Objective: To explore the effects of cytomegalovirus (CMV) infection on rejection-related gene expression in the endothelial cells of renal transplantation recipients.

Methods: Endothelial cells (ECs) were cultured and stimulated by a variety of factors: A, normal control group; B, inactivated human cytomegalovirus (HCMV) infection group; C, HCMV infection group; D, HCMV supernatant infection group; and E, ganciclovir HCMV group. Expression of intercellular adhesion molecule-1 (ICAM-1) and major histocompability complex (MHC) class I and class II antigens was detected by flow cytometry (FCM) and immunohistochemistry.

Results: We found characteristic CMV-infected ECs in this study. There were no significant differences among groups A, B and D (P>0.05). Although the expression levels of ICAM-1 were not significantly different between groups C and E (P>0.05), the ICAM-1 expression in these two groups was significantly higher than that in group A (P<0.05). ICAM-1 expression was detected in groups C and E, while there was no expression in groups A, B and D. Furthermore, there was no significant difference of ICAM-1 mRNA expression between groups C and E (P>0.05). Human leucocyte antigen (HLA)-ABC expression was detected in all the groups, while HLA-DR expression was only detected in groups C and E. There were no significant differences of HLA-ABC and HLA-DR expression among groups A, B and D (P>0.05). However, the HLA-ABC and HLA-DR expression levels in groups C and D were higher than those of the remaining groups previously reported (P<0.05). Meanwhile, the HLA-ABC and HLA-DR expression levels in group E were lower than those of group C (P<0.05).

Conclusion: CMV could up-regulate the expression levels of ICAM-1 and MHC antigens, which was closely related to allograft rejection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Cytomegalovirus / metabolism
  • Cytomegalovirus Infections / complications*
  • Cytomegalovirus Infections / pathology*
  • Endothelial Cells / metabolism*
  • Flow Cytometry / methods
  • Gene Expression Regulation*
  • Graft Rejection*
  • HLA Antigens / biosynthesis*
  • HLA-DR Antigens / metabolism
  • Humans
  • Immunohistochemistry / methods
  • Intercellular Adhesion Molecule-1 / biosynthesis*
  • Kidney Transplantation / adverse effects*
  • Major Histocompatibility Complex
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • HLA Antigens
  • HLA-DR Antigens
  • Intercellular Adhesion Molecule-1