c-Myc and E1A Induced Cellular Sensitivity to Activated NK Cells Involves Cytotoxic Granules as Death Effectors

Oncogene. 1999 Apr 1;18(13):2181-8. doi: 10.1038/sj.onc.1202546.


The contact of natural killer (NK) cells with foreign cells and with certain virus-infected or tumor cells triggers the cytolytic machinery of NK cells. This triggering leads to exocytosis of the cytotoxic NK cell granules. The oncoproteins c-Myc and E1A render cells vulnerable to NK cell mediated cytolysis yet the mechanisms of sensitization are not well understood. In a model where foreign cells (rat fibroblasts) were cocultured with human IL-2 activated NK cells, we observed that NK cells were capable of efficiently killing their targets only if the cells overexpressed the oncogene c-Myc or E1A. Both the parental and the oncogene expressing fibroblasts similarly triggered phosphoinositide hydrolysis in the bound NK cells, demonstrating that NK cells were cytolytically activated in contact with both resistant parental and oncogene expressing sensitive target fibroblasts. The cell death was independent of wild-type p53 and was not inhibited by an anti-apoptotic protein EIB19K. These results provided evidence that c-Myc and E1A activated the NK cell induced cytolysis at a post-triggering stage of NK cell-target cell interaction. In consistence, the c-Myc and E1A overexpressing fibroblasts were more sensitive to the cytolytic effects of isolated NK cell-derived granules than parental cells. The data indicate that oncogenes activate the cytotoxicity of NK cell granules. This mechanism can have a role in directing the cytolytic action of NK cells towards the virus-infected and cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / chemistry
  • Adenovirus E1A Proteins / genetics
  • Adenovirus E1A Proteins / physiology*
  • Animals
  • Apoptosis / genetics
  • Biopolymers
  • Cell Adhesion
  • Cell Membrane / drug effects
  • Cytoplasmic Granules / metabolism*
  • Cytotoxicity, Immunologic / physiology*
  • Exocytosis
  • Fas Ligand Protein
  • Fibroblasts / immunology
  • Genes, myc
  • Genes, p53
  • Humans
  • Interleukin-2 / pharmacology
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology*
  • Membrane Glycoproteins / physiology
  • Phosphatidylinositols / physiology
  • Proto-Oncogene Proteins c-myc / physiology*
  • Rats
  • Recombinant Fusion Proteins / physiology
  • Signal Transduction
  • Transfection
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / physiology
  • Tumor Suppressor Protein p53 / physiology
  • fas Receptor / physiology


  • Actins
  • Adenovirus E1A Proteins
  • Biopolymers
  • FASLG protein, human
  • Fas Ligand Protein
  • Interleukin-2
  • Membrane Glycoproteins
  • Phosphatidylinositols
  • Proto-Oncogene Proteins c-myc
  • Recombinant Fusion Proteins
  • Tnfsf6 protein, rat
  • Tumor Necrosis Factor-alpha
  • Tumor Suppressor Protein p53
  • fas Receptor