Mutant human cells defective in induction of major histocompatibility complex class II genes by interferon gamma

Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2880-4. doi: 10.1073/pnas.90.7.2880.

Abstract

Using immunoselection, we have isolated 11 independent mutant HT1080 fibrosarcoma cell lines defective in the induction by interferon gamma (IFN-gamma) of the expression of the human leukocyte antigen HLA-DRA. The mutations are recessive and fall into five complementation groups. All the mutants are affected mainly in the expression of major histocompatibility complex class II and invariant-chain genes. Type I mutants (three complementation groups) are completely defective in induction of the invariant-chain and class II HLA-DP, -DQ, -DR, and -DM genes, whereas type II mutants (two complementation groups) induce these genes weakly in response to IFN-gamma, in the order DPB > DRA > invariant chain. The induction by IFN-gamma of the mRNAs for class I, TAP1, LMP7, and 9-27 is partially defective and the induction of the proteins IRF-1 and ICAM-1 is normal in both types of mutants. All the mutants respond normally to IFN-alpha. The mutants are stable and thus can be used to clone the affected genes by reversion.

MeSH terms

  • Antibodies, Monoclonal
  • Base Sequence
  • Blotting, Northern
  • Cell Fusion
  • Fibrosarcoma
  • Flow Cytometry
  • Genes, MHC Class II / drug effects*
  • Genes, Recessive
  • Genetic Complementation Test
  • Genetic Markers
  • HLA-D Antigens / analysis
  • HLA-D Antigens / genetics*
  • Humans
  • Interferon-gamma / pharmacology*
  • Molecular Sequence Data
  • Mutagenesis*
  • Oligodeoxyribonucleotides
  • Promoter Regions, Genetic
  • RNA, Messenger / biosynthesis
  • Recombinant Proteins
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Genetic Markers
  • HLA-D Antigens
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • Recombinant Proteins
  • Interferon-gamma