Abstract
The heat shock response is known to inhibit NF-κB activation and NF-κB-dependent gene expression. Herein we determined if cells lacking heat shock factor-1 (HSF-1), the major transcription factor regulating heat shock protein gene expression, have an altered ability to modulate NF-κB activation. Embryonic fibroblasts from HSF-1-null mutant mice (HSF-1-/- cells) had a drastically reduced ability to express heat shock protein-70 in response to heat shock, compared to embryonic fibroblasts from wild-type mice (HSF+/+ cells). There was no difference, however, in the ability of heat shock to inhibit TNFα-mediated NF-κB activation, IκBα degradation, IκB kinase activation, and macrophage chemotactic protein-1 expression in the HSF-1-/- cells compared to the HSF-1+/+ cells. These data demonstrate that heat shock inhibits activation of the NF-κB/IκBα pathway and NF-κB-dependent gene expression in the absence of an intact heat shock response.
Original language | English (US) |
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Pages (from-to) | 453-457 |
Number of pages | 5 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 291 |
Issue number | 3 |
DOIs | |
State | Published - 2002 |
Externally published | Yes |
Keywords
- Cellular activation
- Costimulation
- Heat shock
- Heat shock factor
- Heat shock proteins
- Iκ kinase
- IκBα
- NF-κB
- Transcription factors
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology