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Heat shock inhibits IL-12 p40 expression through NF-kappa B signalling pathway in murine macrophages.

Abstract
We report the effect of heat shock on lipopolysaccharide (LPS)-induced interleukin 12 (IL-12) expression. The augmentation of LPS-induced IL-12 p40 mRNA and p70 protein was significantly suppressed in both peritoneal macrophages and RAW264.7 cells after heat shock at 43 degrees C. The binding activity of nuclear factor kappa B (NF-kappa B) was reduced by prior heat shock. LPS did not induce degradation of the inhibitory protein I-kappa B alpha in the shocked cells, which might be a potential mechanism to block NF-kappa B activation. Furthermore, transient transfection assay in RAW264.7 cells demonstrated that LPS-induced activation of DM703 and DM138 (contains NF-kappa B motif) was highly sensitive to heat shock. These data suggest that heat shock influences expression of IL-12 through the I-kappa B/NF-kappa B pathway.
AuthorsC L Li, X Y Wang, J Shao, J S Zhang, W G Feng, Y B Wang, Z L Chang
JournalCytokine (Cytokine) Vol. 16 Issue 4 Pg. 153-9 (Nov 21 2001) ISSN: 1043-4666 [Print] England
PMID11792125 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2001 Academic Press.
Chemical References
  • DNA-Binding Proteins
  • I-kappa B Proteins
  • Interleukin-12 Subunit p40
  • Lipopolysaccharides
  • NF-kappa B
  • Nfkbia protein, mouse
  • Protein Subunits
  • RNA, Messenger
  • NF-KappaB Inhibitor alpha
  • Interleukin-12
Topics
  • Animals
  • Binding Sites (genetics)
  • Cell Line
  • DNA-Binding Proteins (metabolism)
  • Gene Expression
  • Hot Temperature
  • I-kappa B Proteins
  • In Vitro Techniques
  • Interleukin-12 (biosynthesis, genetics)
  • Interleukin-12 Subunit p40
  • Lipopolysaccharides (pharmacology)
  • Macrophages (drug effects, immunology, metabolism)
  • Macrophages, Peritoneal (drug effects, immunology, metabolism)
  • Mice
  • NF-KappaB Inhibitor alpha
  • NF-kappa B (metabolism)
  • Promoter Regions, Genetic
  • Protein Subunits
  • RNA, Messenger (genetics, metabolism)
  • Signal Transduction

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