Quantitative modifications of major histocompatibility complex (MHC) antigens induced by recombinant gamma interferon in two human breast cancer lines

Int J Immunopharmacol. 1987;9(4):459-68. doi: 10.1016/0192-0561(87)90020-8.

Abstract

H466-B and T47-D breast carcinoma cell lines were treated with recombinant gamma interferon (r gamma IFN) to study major histocompatibility complex (MHC) class I and class II antigen responses. Untreated H466-B cells released B2 microglobulin (B2M) into the culture medium and expressed B2M and class I heavy chain on 100% of the cells. The expression of class II antigens (DR) was limited to 8 +/- 4% of the cells. This subpopulation was isolated by cell sorting and labelled with 35S methionine. Protein extracts were immunoprecipitated with anti-DR antibody and subjected to two dimensional non-equilibrium pH gradient electrophoresis (2D-PAGE). A normal pattern of expression of invariant, alpha and beta chains was shown. The MHC antigenic expression of H466-B parental cell line was not modified by interferon treatment. Untreated T47-D cells did not release B2M into the culture medium, expressed B2M and class I heavy chain on 100% of the cells but did not express class II molecules using radio-immunoassay or 2D-PAGE. As early as 24 h after r gamma IFN addition, T47-D cells released B2M into the medium, B2M and class I heavy chain were significantly greater than that of untreated cells, and class II antigenic expression was found, all these in a dose dependent manner. 2D-PAGE analysis of class II antigens revealed the profile of human DR molecules but this expression seemed incomplete since only single alpha and beta spots were detected suggesting a possible defect in the sialilation of DR molecules. These results show a heterogeneity in MHC antigenic responses to r gamma IFN and suggest that synthetized class II molecules may be incompletely processed.

MeSH terms

  • Antibodies, Monoclonal
  • Antigens, Neoplasm / analysis
  • Breast Neoplasms / immunology*
  • Cell Division / drug effects
  • Cell Line
  • HLA Antigens / analysis*
  • HLA-D Antigens / analysis
  • Humans
  • Interferon-gamma / pharmacology*
  • Isoelectric Point
  • Major Histocompatibility Complex*
  • Molecular Weight
  • beta 2-Microglobulin / metabolism

Substances

  • Antibodies, Monoclonal
  • Antigens, Neoplasm
  • HLA Antigens
  • HLA-D Antigens
  • beta 2-Microglobulin
  • Interferon-gamma