Major histocompatibility complex class I-independent killing of xenogeneic targets by rat allospecific natural killer cells

Transplantation. 1997 Jan 15;63(1):119-23. doi: 10.1097/00007890-199701150-00022.

Abstract

Major histocompatibility complex class I molecules can inhibit mouse as well as human natural killer (NK) cell cytotoxicity. In contrast, antigens encoded in the RT1.C region of the rat MHC gene complex have been suggested to trigger, rather than inhibit, rat NK cells. In an attempt to analyze rat NK cell specificity, with respect to the cross-species difference that may exist in NK cell-mediated cytotoxicity, we investigated the ability of interleukin 2-activated, allospecific rat NK cells to recognize MHC class I-positive and -deficient target cells of mouse and human origins. Recognition of xenogeneic target cells by rat allospecific NK cells was found to be MHC class I independent; target cell MHC class I was not required for killing, and expression of different sets of mouse and human MHC class I molecules did not influence the cytotoxic response. These results indicate that rat NK cells can recognize xenogeneic nontransformed cells by mechanisms not related to target cell MHC class I expression, and that mouse and human MHC class I molecules, at least among those tested in this study, are unable to confer inhibition of rat NK cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytotoxicity, Immunologic*
  • Haplotypes
  • Histocompatibility Antigens Class I / physiology*
  • Humans
  • Interleukin-2 / pharmacology
  • Killer Cells, Natural / immunology*
  • Major Histocompatibility Complex
  • Mice
  • Rats

Substances

  • Histocompatibility Antigens Class I
  • Interleukin-2