| Project/Area Number |
04671542
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Hematology
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| Research Institution | NATIONAL INSTITUTE OF RADIOLOGICAL SCIENCES |
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Principal Investigator |
AKASHI Makoto NIRS,Radiat Health, Section Head, 障害・臨床研究部, 室長 (10222514)
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| Co-Investigator(Kenkyū-buntansha) |
HACHIYA Misao NIRS,Radiat Health, 障害・臨床研究部, 研究員 (00198756)
KAWASE Yoshiko NIRS,Radiat Health, 障害・臨床研究部, 主任研究官 (20161325)
SUZUKI Gen NIRS,Radiat Health, Section Head, 障害・臨床研究部, 室長 (00179201)
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| Project Period (FY) |
1992 – 1994
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| Project Status |
Completed (Fiscal Year 1994)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1994: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1993: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1992: ¥1,100,000 (Direct Cost: ¥1,100,000)
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| Keywords | human fibroblasts / GM-CSF / autocrine stimulationm / mRNA / constitutive expression / 自己刺激 / 線維芽細胞 |
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| Research Abstract |
Prior study by us found that expression of GM-CSF mRNA in human embryonic lung fibroblasts W138 is regulated through an autocrine stimulation by IL-1 production. In the present study, we showed that expression of manganese superoxide dismutase (MnSOD) gene is also regulated by an autocrine mechanism in these cells ; treatment of cells with either anti-IL-1 alpha or beta antibody reduced the constitutive expession of MnSOD mRNA.These results indicate that the autocrine stimulation may be one of the important mechanisms in expression of genes as well as GM-CSF.To further investigate the role of IL-1 in induction of GM-CSF or MnSOD,cells were irradiated in the presence of anti-IL-1 antibody. Irradiation increased the levels of GM-CSF and MnSOD mRNAs in a dose- and time-dependent fashion. Treatment with anti-IL-1 antibody blocked the induction of these mRNAs in these cells and exogenously added-IL-1 increased the levels of these mRNAs. Similar results were also obtained in the experiment using human monocytic cells THP-1. Irradiation increased the production of tumor necrosis factor (TNF) in a dose dependent manner. Irradiation induced the expression of MnSOD mRNA and treatment of these cells with anti-TNF antibody inhibited the induction of MnSOD mRNA by irradiation. Furthermore, we also found that irradiation increased expression of WAF1/CIP1, p21, through the production of TNF in human myeloblastic cells KG1. Our present studies indicate an autocrine or paracrine mechanism (s) may play an important role in expression of genes in various cells.
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