ARACHIDONATE IS A POTENT MODULATOR OF HUMAN HEAT-SHOCK GENE-TRANSCRIPTION

DA JURIVICH, Lea Sistonen, KD SARGE, RI MORIMOTO

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    Sammanfattning

    Cell and tissue injury activate the inflammatory response through the action(s) of arachidonic acid and its metabolites, leading to the expression of acute-phase proteins and inflammatory cytokines. At the molecular level, little is known how arachidonic acid regulates the inflammatory response. As inflammation is also associated with local increase in tissue temperatures, we examined whether arachidonic acid was directly involved in the heat shock response. Extracellular exposure to arachidonic acid induced heat shock gene transcription in a dose-dependent manner via acquisition of DNA-binding activity and phosphorylation of heat shock factor 1 (HSF1). In addition, exposure of cells to low concentrations of arachidonic acid, which by themselves did not induce HSF1 DNA-binding activity, reduced the temperature threshold for HSF1 activation from elevated temperatures which are not physiologically relevant (>42 degrees C) to temperatures which can be attained during the febrile response (39-40 degrees C). These results indicate that elevated heat shock gene expression is a direct consequence of an arachidonic acid-mediated cellular response.
    OriginalspråkOdefinierat/okänt
    Sidor (från-till)2280–2284
    Antal sidor5
    TidskriftProceedings of the National Academy of Sciences
    Volym91
    Utgåva6
    StatusPublicerad - 1994
    MoE-publikationstypA1 Tidskriftsartikel-refererad

    Nyckelord

    • HEAT SHOCK TRANSCRIPTION FACTORS
    • INFLAMMATION
    • PHOSPHORYLATION

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