A membrane-located glycosphingolipid of monocyte/granulocyte lineage cells induces growth arrest and triggers the lytic viral cycle in Epstein-Barr virus genome-positive Burkitt lymphoma lines

Med Microbiol Immunol. 1999 Aug;188(1):23-9. doi: 10.1007/s004300050101.

Abstract

Gangliosides are known to influence cell growth and differentiation. The neolacto series ganglioside IV3NeuAc-nLc4 (2-->3-sialosylparagloboside) is present in members of the monocyte/granulocyte lineage, but is not found in cells that belong to the lymphocyte lineage. In this study we demonstrated that IV3NeuAc-nLc4 inhibits the proliferation of Epstein-Barr virus (EBV) genome-positive Burkitt lymphoma cells of the lines Raji and P3HR-1K. IV3NeuAc-nLc4-induced growth inhibition is associated with an increase in G0/G1 phase cells and a reduced expression of CD21 and HLA-DR antigens on Raji cells. These data suggest that IV3NeuAc-nLc4 may affect differentiation of lymphoma cells. Additionally, the increased expression of viral mRNA species which are characteristic for the lytic viral cycle in the non-producer line Raji and the enhanced release of virions from the producer line P3HR-1K demonstrate that IV3NeuAc-nLc4 activates the replication of EBV. Growth inhibition and termination of the viral latency suggest that IV3NeuAc-nLc4 present in monocyte/granulocyte lineage cells may be an effector of the natural defense against EBV persistency and transformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • B-Lymphocytes / physiology*
  • B-Lymphocytes / virology
  • Burkitt Lymphoma / pathology*
  • Burkitt Lymphoma / virology*
  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • Cell Lineage
  • Cell Membrane / chemistry
  • Flow Cytometry
  • Globosides / pharmacology*
  • Granulocytes / chemistry
  • Herpesvirus 4, Human / drug effects
  • Herpesvirus 4, Human / physiology*
  • Humans
  • Monocytes / chemistry
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured
  • Viral Proteins / genetics
  • Viral Proteins / metabolism
  • Virus Latency / drug effects
  • Virus Replication / drug effects

Substances

  • Globosides
  • RNA, Messenger
  • Viral Proteins
  • sialosylparagloboside