TNF and CD95 promote IL-8 gene transactivation via independent elements in colon carcinoma cells

Cytokine. 2001 Jul 21;15(2):108-12. doi: 10.1006/cyto.2001.0915.

Abstract

The pro-inflammatory cytokine interleukin-8 (IL-8) is produced by HT29 colon epithelial cells following engagement of either CD95 or tumour necrosis factor (TNF) receptors. While the IL-8 promotor elements activated by TNF are well characterised, those responsible for induction of IL-8 by CD95 are unknown. We examined the pathway for CD95 induced IL-8 secretion using two luciferase reporter constructs; the first comprising approximately 500 bp of the IL-8 promotor that includes the nuclear factor kappa B (NFkappaB), C/EBP and AP-1 sites known to be involved in TNF mediated IL-8 induction; the second that encompasses these elements but extends approximately 1.1 kb further upstream. Although IL-8 mRNA and protein were produced in response to either TNF or CD95 ligation, only TNF induced an increase in the reporter activity of the promoter constructs. Nevertheless, IL-8 induction by CD95 resulted primarily from increased transcription and not from an increase in IL-8 mRNA stability. These results suggest that promoter elements/enhancers involved in CD95 mediated IL-8 induction are distinct from those used by TNF and not contained within the 1.6 kb region immediately upstream of the initiation codon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Colon / metabolism
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism*
  • HT29 Cells
  • Humans
  • Interferon-gamma
  • Interleukin-8 / agonists
  • Interleukin-8 / genetics*
  • Interleukin-8 / metabolism*
  • Intestinal Mucosa / metabolism
  • RNA, Messenger / metabolism
  • Receptors, Tumor Necrosis Factor / immunology
  • Receptors, Tumor Necrosis Factor / metabolism*
  • Signal Transduction
  • Transcriptional Activation* / drug effects
  • Transcriptional Activation* / immunology
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology
  • fas Receptor / immunology
  • fas Receptor / metabolism*
  • fas Receptor / pharmacology

Substances

  • Interleukin-8
  • RNA, Messenger
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Interferon-gamma