Different levels of control prevent interferon-gamma-inducible HLA-class II expression in human neuroblastoma cells

Oncogene. 2003 Oct 30;22(49):7848-57. doi: 10.1038/sj.onc.1207054.

Abstract

The HLA class II expression is controlled by the transcriptional activator CIITA. The transcription of CIITA is controlled by different promoters, among which promoter-IV is inducible by IFN-gamma. We analysed the regulation of HLA class II molecules by IFN-gamma in a large series of human neuroblastoma cell lines. No induction of surface or intracellular HLA class II molecules and of specific mRNA was observed, in all neuroblastomas, with the exception of a nonprototypic cell line, ACN. In a large subset of neuroblastomas IFN-gamma induced expression of CIITA mRNA, derived from promoter-IV, which was not methylated. In contrast, in another subset of neuroblastomas, CIITA was not inducible by IFN-gamma and CIITA promoter-IV was either completely or partially methylated. Interestingly, the use of DNA demethylating agents restored CIITA gene transcriptional activation by IFN-gamma, but not HLA class II expression. The defect of HLA class II was not related to alterations in RFX or NF-Y transcription factors, as suggested by EMSA or RFX gene transfection experiments. In addition, the transfection of a functional CIITA cDNA failed to induce HLA class II expression in typical neuroblastoma cells. Confocal microscopy and Western blot analysis suggested a defective nuclear translocation and/or reduced protein synthesis in CIITA-transfected NB cells. Altogether, these data point to multiple mechanisms preventing HLA class II expression in the neuroblastoma, either involving CIITA promoter-IV silencing, or acting at the CIITA post-transcriptional level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • DNA Methylation
  • DNA-Binding Proteins / analysis
  • Gene Expression Regulation / drug effects
  • Histocompatibility Antigens Class II / analysis*
  • Histocompatibility Antigens Class II / genetics
  • Humans
  • Interferon Regulatory Factor-1
  • Interferon-gamma / pharmacology*
  • Neuroblastoma / immunology*
  • Neuroblastoma / pathology
  • Nuclear Proteins*
  • Phosphoproteins / analysis
  • Promoter Regions, Genetic
  • RNA, Messenger / analysis
  • Trans-Activators / genetics*
  • Trans-Activators / physiology
  • Transcription Factors / analysis
  • Transfection
  • Upstream Stimulatory Factors

Substances

  • DNA-Binding Proteins
  • Histocompatibility Antigens Class II
  • IRF1 protein, human
  • Interferon Regulatory Factor-1
  • MHC class II transactivator protein
  • Nuclear Proteins
  • Phosphoproteins
  • RNA, Messenger
  • Trans-Activators
  • Transcription Factors
  • Upstream Stimulatory Factors
  • Interferon-gamma