Expression and function of Qa-2 major histocompatibility complex class I molecules in transgenic mice

Int Immunol. 1991 May;3(5):493-502. doi: 10.1093/intimm/3.5.493.

Abstract

Qa-2 molecules are weak transplantation antigens encoded by class I genes of the major histocompatibility complex. When expressed in transgenic CBA mice, Qa-2 molecules provoke rapid rejection of skin grafts and strong, Qa-2 specific, cytotoxic T-cell responses. Efficient rejection of skin grafts from Qa-2 transgenic mice takes place when Qa-2 molecules are attached to the cell membrane with a glycophosphatidyl anchor or by a transmembrane protein domain, except that rejection times are slightly longer in the former case. These results demonstrate that Qa-2 molecules can behave as major transplantation antigens, as do closely related H-2 molecules. Failure of Qa-2 molecules to provoke strong T-cell responses in non-transgenic mice is probably due to the very low level of expression of Qa-2 molecules in skin keratinocytes from such mice since these cells express increased levels of Qa-2 molecules in all Qa-2 transgenic mice.

MeSH terms

  • Animals
  • Female
  • Gene Expression Regulation
  • Genes, MHC Class I*
  • Genes, Synthetic
  • Graft Rejection
  • H-2 Antigens / biosynthesis*
  • H-2 Antigens / genetics
  • H-2 Antigens / immunology
  • Histocompatibility Antigen H-2D
  • Histocompatibility Antigens Class I / biosynthesis*
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology
  • Keratinocytes / immunology
  • Male
  • Mice
  • Mice, Inbred CBA / genetics
  • Mice, Inbred CBA / immunology
  • Mice, Transgenic / immunology
  • Protein Engineering
  • Recombinant Fusion Proteins / biosynthesis*
  • Recombinant Fusion Proteins / immunology
  • Skin Transplantation / immunology
  • T-Lymphocytes, Cytotoxic / immunology
  • Transcription, Genetic

Substances

  • H-2 Antigens
  • Histocompatibility Antigen H-2D
  • Histocompatibility Antigens Class I
  • Q surface antigens
  • Recombinant Fusion Proteins