Lack of HLA-class I antigens in human neuroblastoma cells: analysis of its relationship to TAP and tapasin expression

Tissue Antigens. 2001 Feb;57(2):110-7. doi: 10.1034/j.1399-0039.2001.057002110.x.

Abstract

We studied the constitutive and the interferon (IFN)-gamma-induced expression of HLA class I antigen heavy chain, beta2-microglobulin (beta2m), TAP-1, TAP-2 and tapasin in a panel of eleven neuroblastoma cell lines. Surface expression of HLA class I antigens was low in eight out of eight neuroblastoma cell lines bearing MYC-N amplification and/or 1p deletion, while two out of three neuroblastoma cell lines lacking these genetic alterations showed normal expression. IFN-gamma treatment restored HLA class I antigen surface expression in all neuroblastoma cell lines. Eight out of 11 neuroblastoma cell lines did not express TAP-1 mRNA and three of them also lacked TAP-2 mRNA. beta2 m mRNA was barely detectable or absent in five neuroblastoma cell lines, while tapasin mRNA was always expressed. IFN-gamma upregulated the expression of HLA class I heavy chain, beta2 m, TAP-1, TAP-2 and tapasin, as detected at mRNA or protein level. Post-transcriptional events were involved in altered TAP-1 and beta2 m expression in one peculiar neuroblastoma cell line. These data indicate that multiple mechanisms play a role in the HLA class I antigen-deficient phenotype of human neuroblastoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • ATP-Binding Cassette Transporters / analysis
  • ATP-Binding Cassette Transporters / genetics*
  • ATP-Binding Cassette Transporters / immunology
  • Antigens, Surface / genetics
  • Antigens, Surface / immunology
  • Antineoplastic Agents / pharmacology
  • Antiporters / analysis
  • Antiporters / genetics*
  • Antiporters / immunology
  • Blotting, Western
  • Brain Neoplasms / immunology*
  • Extracellular Matrix Proteins / analysis
  • Extracellular Matrix Proteins / genetics*
  • Extracellular Matrix Proteins / immunology
  • Gene Deletion
  • Gene Expression / drug effects
  • Gene Expression / immunology
  • Genes, myc
  • Histocompatibility Antigens Class I / analysis
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Immunoglobulin Heavy Chains / analysis
  • Immunoglobulin Heavy Chains / genetics
  • Immunoglobulin Heavy Chains / immunology
  • Immunoglobulins / analysis
  • Immunoglobulins / genetics*
  • Immunoglobulins / immunology
  • Interferon-gamma / pharmacology
  • Membrane Transport Proteins
  • Nerve Tissue Proteins / analysis
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / immunology
  • Neuroblastoma / immunology*
  • RNA, Messenger / analysis
  • Tumor Cells, Cultured
  • beta 2-Microglobulin / analysis
  • beta 2-Microglobulin / genetics
  • beta 2-Microglobulin / immunology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • ATP-Binding Cassette Transporters
  • Antigens, Surface
  • Antineoplastic Agents
  • Antiporters
  • Extracellular Matrix Proteins
  • Histocompatibility Antigens Class I
  • Immunoglobulin Heavy Chains
  • Immunoglobulins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • RNA, Messenger
  • TAP1 protein, human
  • beta 2-Microglobulin
  • tapasin
  • TAP2 protein, human
  • Interferon-gamma