Epstein-Barr virus nuclear antigen 2 induces interleukin-18 receptor expression in B cells

Blood. 2005 Feb 15;105(4):1632-9. doi: 10.1182/blood-2004-08-3196. Epub 2004 Oct 21.

Abstract

Epstein-Barr virus (EBV) latently infects and immortalizes B lymphocytes and causes lymphoproliferative malignancies. We show here that the EBV nuclear antigen EBNA2 induces expression of the 2 chains of the interleukin-18 receptor (IL-18R) in Burkitt lymphoma (BL) cell lines and in nontransformed B cells. Activation of IL-18R expression by EBNA2 is independent of its interaction with the transcriptional repressor RBPJ kappa. It occurs in the absence of any other viral protein but requires de novo synthesis of cellular proteins. IL-18R induction is a highly specific function of EBNA2, because neither other EBV latent proteins nor the cellular proteins c-myc or Notch can exert this effect. Using cDNA microarray expression profiling, we find that the IL-18 receptor expressed in EBV-infected BL cells has signaling capacity, because IL-18 significantly modified gene expression. We report that EBNA2 expression is associated with IL-18R expression in vivo in EBV-positive B-lymphomas from AIDS patients.

Publication types

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

MeSH terms

  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism*
  • B-Lymphocytes / virology
  • Burkitt Lymphoma / immunology
  • Burkitt Lymphoma / metabolism
  • Burkitt Lymphoma / virology
  • Cell Line, Transformed
  • Cell Line, Tumor
  • Epstein-Barr Virus Nuclear Antigens / biosynthesis
  • Epstein-Barr Virus Nuclear Antigens / physiology*
  • Gene Expression Regulation, Viral / immunology
  • Genes, Viral
  • Herpesvirus 4, Human / genetics
  • Humans
  • Interleukin-18 Receptor alpha Subunit
  • Lymphoma, AIDS-Related / immunology
  • Lymphoma, AIDS-Related / metabolism
  • Lymphoma, AIDS-Related / virology
  • Lymphoma, Large B-Cell, Diffuse / immunology
  • Lymphoma, Large B-Cell, Diffuse / metabolism
  • Lymphoma, Large B-Cell, Diffuse / virology
  • Protein Subunits / biosynthesis
  • Protein Subunits / metabolism
  • Receptors, Interleukin / biosynthesis*
  • Receptors, Interleukin / metabolism
  • Receptors, Interleukin / physiology
  • Receptors, Interleukin-18
  • Viral Proteins
  • Viral Structural Proteins / genetics

Substances

  • EBNA-2 protein, Human herpesvirus 4
  • Epstein-Barr Virus Nuclear Antigens
  • IL18R1 protein, human
  • Interleukin-18 Receptor alpha Subunit
  • Protein Subunits
  • Receptors, Interleukin
  • Receptors, Interleukin-18
  • Viral Proteins
  • Viral Structural Proteins