Listeria monocytogenes infection enhances transcription factor NF-kappa B in P388D1 macrophage-like cells

Infect Immun. 1994 Jul;62(7):2740-7. doi: 10.1128/iai.62.7.2740-2747.1994.

Abstract

In the present study, we investigated the effect of Listeria monocytogenes infection on the cellular level of the transcription factors NF-kappa B, AP-1, and NF-IL6 in the macrophage-like cell line P388D1 by using electrophoretic mobility shift assays. Infection with L. monocytogenes enhanced the formation of two NF-kappa B-like DNA-protein complexes, C1 and C2, whereas the concentration of AP-1 and NF-IL6 complexes remained unaffected. In supershift assays using NF-kappa B-specific antibodies, complex C2 was identified to be a p50 homodimer (KBF1) and complex C1 was identified as a p50/p65 heterodimer. Both complexes were formed within 10 min after addition of the bacteria. Since the synthesis of tumor necrosis factor alpha and interleukin-1 occurs at later times, these cytokines cannot be the mediators of enhanced NF-kappa B formation. Infection experiments with different nonhemolytic mutants of L. monocytogenes and the use of the phagocytosis inhibitor cytochalasin B suggest that events prior to invasion and escape of the bacteria from the phagosome into the cytoplasm enhance the nuclear transport of p50/p65 NF-kappa B components.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • CCAAT-Enhancer-Binding Proteins
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Cytochalasin B / pharmacology
  • DNA-Binding Proteins / metabolism
  • Interleukin-1 / pharmacology
  • Listeria / genetics
  • Listeria / growth & development
  • Listeria / pathogenicity
  • Listeria monocytogenes / genetics
  • Listeria monocytogenes / growth & development*
  • Listeria monocytogenes / pathogenicity
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Mice
  • Molecular Sequence Data
  • NF-kappa B / biosynthesis*
  • Nuclear Proteins / metabolism
  • Phagocytosis / drug effects
  • Protein Binding
  • Proto-Oncogene Proteins c-jun / metabolism
  • Transcription Factors / biosynthesis*
  • Tumor Necrosis Factor-alpha / pharmacology
  • Virulence

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • Interleukin-1
  • NF-kappa B
  • Nuclear Proteins
  • Proto-Oncogene Proteins c-jun
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Cytochalasin B