Initial characterization of the apoptosis-inducing receptor for natural human anti-neuroblastoma IgM

Med Pediatr Oncol. 2001 Jan;36(1):251-7. doi: 10.1002/1096-911X(20010101)36:1<251::AID-MPO1062>3.0.CO;2-Z.

Abstract

Background: Human neuroblastoma (NB) cells contain a 260 kDa surface antigen (NB-p260), which serves as receptor for natural human IgM antibodies (anti-NB IgM). Upon binding to NB-p260, these antibodies induce apoptosis in human NB cells.

Procedure and results: In this study, we purified NB-p260 to homogeneity from human LA-N-1 NB cells by sequential ion exchange chromatography followed by preparative SDS gel electrophoresis. Purified NB-p260 exhibited rapid autodegradation despite the presence of various protease inhibitors. The autodegradation process precluded extensive N-terminal sequencing. However, from repeat N-terminal sequence analysis, a consensus sequence of seven amino acid residues emerged that exhibited significant homology to the subunit c of the human mitochondrial ATP synthase, a hydrophobic membrane protein of 7.6 kDa. Western blot analyses demonstrated that purified NB-p260 was recognized by polyclonal antibodies raised against both subunit c-containing storage bodies and a synthetic peptide consisting of amino acid residues 32-45 of subunit c. In addition to peptide sequences related to subunit c, NB-p260 also contained epitopes related to the human heat shock protein HSP90. In Western blots, a monoclonal anti-HSP90 antibody reacted with purified NB-p260 as well as with a predominant protein fragment of approximately 90 kDa that appeared during the process of NB-p260 autodegradation. The anti-HSP90 antibody was also capable of binding to the surface of LA-N-1 cells and inhibiting the binding of human anti-NB IgM in a dose-dependent manner.

Conclusions: Collectively, our data suggest that NB-p260, the apoptosis-mediating receptor for natural human anti-NB IgM, represents a novel surface protein of human NB cells containing polypeptide sequences related to the subunit c of the mitochondrial ATP synthase and the heat shock protein HSP90.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Neoplasm / immunology*
  • Antibody Specificity
  • Antigens, Neoplasm / chemistry
  • Antigens, Neoplasm / immunology*
  • Antigens, Neoplasm / isolation & purification
  • Apoptosis / immunology*
  • Blotting, Western
  • Chromatography, Ion Exchange
  • Electrophoresis, Polyacrylamide Gel
  • Flow Cytometry
  • HSP90 Heat-Shock Proteins / chemistry
  • Humans
  • Immune Sera
  • Immunity, Innate
  • Immunoglobulin M / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Neuroblastoma / immunology
  • Neuroblastoma / pathology*
  • Peptide Fragments / chemistry
  • Peptide Fragments / immunology
  • Protease Inhibitors / pharmacology
  • Proton-Translocating ATPases / chemistry
  • Sequence Analysis, Protein
  • Sequence Homology, Amino Acid
  • Tumor Cells, Cultured / immunology

Substances

  • Antibodies, Neoplasm
  • Antigens, Neoplasm
  • HSP90 Heat-Shock Proteins
  • Immune Sera
  • Immunoglobulin M
  • NB-p260 antigen
  • Peptide Fragments
  • Protease Inhibitors
  • Proton-Translocating ATPases