Regulation of tumour necrosis factor α mRNA stability by the mitogen-activated protein kinase p38 signalling cascade

Matthew Brook, Gareth Sully, Andrew R. Clark*, Jeremy Saklatvala

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

192 Citations (Scopus)

Abstract

The translation of tumour necrosis factor α (TNFα) mRNA is regulated by the stress-activated protein kinase p38, which also controls the stability of several pro-inflammatory mRNAs. The regulation of TNFα gene expression in a mouse macrophage cell line RAW264.7 was re-examined using an inhibitor of stress-activated protein kinases. Stimulation of these cells with bacterial lipopolysaccharide resulted in stabilisation of TNFα mRNA, which was reversed by specific inhibition of p38. An adenosine/uridine-rich element from the TNFα 3' untranslated region conferred p38-sensitive decay in a tetracycline-regulated mRNA stability assay. Therefore the p38 pathway also controls TNFα mRNA turnover. Copyright (C) 2000 Federation of European Biochemical Societies.

Original languageEnglish
Pages (from-to)57-61
Number of pages5
JournalFEBS Letters
Volume483
Issue number1
DOIs
Publication statusPublished - 13 Oct 2000

Keywords

  • Lipopolysaccharide
  • Macrophage
  • Mitogen-activated protein kinase p38
  • mRNA stability
  • Translation
  • Tumor necrosis factor α

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Cell Biology

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