The role of NF-kappa B and NF-IL6 transactivating factors in the synergistic activation of human serum amyloid A gene expression by interleukin-1 and interleukin-6

J Biol Chem. 1993 Dec 5;268(34):25624-31.

Abstract

To understand the mechanisms by which large increases in serum amyloid A (SAA) occur during the acute phase response, human hepatoma cells were transfected with SAA2 gene reporter plasmids and stimulated with combinations of cytokines. Although interleukin-1 (IL-1) and interleukin-6 (IL-6) stimulated transcription from this promoter individually, addition of both mediators produced a response between two and nine times greater than the expected additive response. This synergistic activation was dependent on the integrity of at least two cis-acting sequences in the SAA2 enhancer. The SAA2 NF-kappa B site was required functionally for the response to both IL-1 and IL-6 alone as well as for synergistic activation; however, IL-6 did not directly induce binding of nuclear proteins to the NF-kappa B sequence. A NF-IL6 site was required for full induction by IL-1 and IL-6, and also mediated strong transactivation by recombinant NF-IL6. Furthermore, transfected NF-IL6 synergized strongly with co-transfected NF-kappa B, particularly with RelA (p65). However synergy between IL-1 and IL-6 was only partly reduced by mutation of the NF-IL6 site, indicating further levels of interaction in addition to the NF-kappa B/NF-IL6 cooperativity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites
  • CCAAT-Enhancer-Binding Proteins
  • Cell Nucleus / metabolism
  • DNA-Binding Proteins / metabolism*
  • Drug Synergism
  • Gene Expression / drug effects
  • Gene Expression / physiology*
  • Humans
  • Interleukin-1 / pharmacology*
  • Interleukin-6 / pharmacology*
  • Kinetics
  • Methylation
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • NF-kappa B / biosynthesis
  • NF-kappa B / metabolism*
  • Nuclear Proteins / metabolism*
  • Oligodeoxyribonucleotides
  • Protein Biosynthesis
  • Serum Amyloid A Protein / biosynthesis*
  • Transcription Factors / metabolism*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • Interleukin-1
  • Interleukin-6
  • NF-kappa B
  • Nuclear Proteins
  • Oligodeoxyribonucleotides
  • Serum Amyloid A Protein
  • Transcription Factors