Immediately after X-irradiation, monocytic cells can express the gene for interleukin (IL)-1beta, which enhances inflammation and contributes to radioprotection in mice. In order to analyze the mechanism(s) for the immediate-early induction of IL-1beta after X-irradiation at 20 Gy in cultured murine macrophages, we examined the molecules that bound to the DNA fragments corresponding to the upstream region of 10 kb of the mouse IL-1beta gene using an electrophoretic mobility-shift assay. Three DNA fragments corresponding to the 8,500, 8,000 and 2,500 bases upstream of the gene showed an unique binding site with the nuclear extract. Specific binding activity with these DNA fragments was observed in the nuclear extract from non-irradiated cells, and disappeared upon a pretreatment of the extract with proteinase K. The binding activity was not detected in the nuclear extract from irradiated cells. This shows that protein(s) specifically binding to the far-upstream regions of the IL-1beta gene disappear immediately after X-irradiation in the nuclei of macrophage cells, and that the event is potentially related to the immediate-early response of IL-1beta gene expression.
Disappearance of nuclear binding proteins specifically bound to the upstream region of the interleukin-1beta gene immediately after irradiation of mouse macrophages.
H. Ishihara,I. Tanaka,H. Wan,C. Cheeramakara
Published 2003 in Journal of Radiation Research
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- Publication year
2003
- Venue
Journal of Radiation Research
- Publication date
2003-06-01
- Fields of study
Biology, Medicine
- Identifiers
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- Source metadata
Semantic Scholar, PubMed
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