Publication: Disappearance of nuclear binding proteins specifically bound to the upstream region of the interleukin-1β gene immediately after irradiation of mouse macrophages
Issued Date
2003-06-01
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ISSN
04493060
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2-s2.0-2942543467
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Mahidol University
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SCOPUS
Bibliographic Citation
Journal of Radiation Research. Vol.44, No.2 (2003), 117-123
Suggested Citation
Hiroshi Ishihara, Izumi Tanaka, Hong Wan, Cheerarattana Cheeramakara Disappearance of nuclear binding proteins specifically bound to the upstream region of the interleukin-1β gene immediately after irradiation of mouse macrophages. Journal of Radiation Research. Vol.44, No.2 (2003), 117-123. doi:10.1269/jrr.44.117 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/20850
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Title
Disappearance of nuclear binding proteins specifically bound to the upstream region of the interleukin-1β gene immediately after irradiation of mouse macrophages
Abstract
Immediately after X-irradiation, monocytic cells can express the gene for interleukin (IL)-1β, which enhances inflammation and contributes to radioprotection in mice. In order to analyze the mechanism(s) for the immediate-early induction of IL-1β 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-1β 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-1β 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-1β gene expression.