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The role of MHC class I expression in rat NK cell-mediated lysis of syngeneic tumor cells and virus-infected cells

  • Katinka M. Giezeman-Smits
  • , Peter J.K. Kuppen
  • , N. Geeske Ensink
  • , Alexander M.M. Eggermont
  • , Frans Stals
  • , Kurt Wonigeit
  • , Gert Jan Fleuren

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)

Abstract

In this study the role of MHC class I antigen expression in rat natural killer (NK) cell-mediated lysis was investigated. Various rat tumor cell lines and two Adenovirus (Ad)-transformed rat cell lines were tested for their expression levels of total MHC class I and two MHC class I alleles, RT1.A and RT1.C, by flow cytometry. Their susceptibility to NK cell-mediated lysis in relation to MHC class I expression was determined by 51Cr release assays. IFN-γ is know to increase the expression of MHC class I. Therefore target cell with and without prior IFN-γ treatment were examined for MHC class I expression and its effect on NK lysis. An significant inverse exponential relationship was found. To investigate the effect of virus infection on MHC class I expression and target cell lysis by NK cells, rat embryonal fibroblasts (REF) were infected with cytomegalovirus (CMV) and used as target cells for NK cell-mediated lysis. Results showed chat these virus-infected cells were less susceptible to NK lysis than non-infected cells. Moreover, the non-infected cells expressed less MHC class I than the infected cells, indicating that also in this case, there was an inverse correlation between MHC class I expression and susceptibility to lysis by NK cells. Subsequently, we showed that sorted subsets of predominantly CD8-positive and CD8-negative NK cells lysed a MHC class I-positive tumor cell line at the same level. This suggests that CD8 is not likely to participate as a receptor for MHC class I in NI( cell-mediated lysis in a syngeneic rat model.

Original languageEnglish
Pages (from-to)286-299
Number of pages14
JournalImmunobiology
Volume195
Issue number3
DOIs
Publication statusPublished - Aug 1996
Externally publishedYes

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