| Project/Area Number |
13670246
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
寄生虫学(含医用動物学)
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| Research Institution | Tottori University |
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Principal Investigator |
FUKUMOTO Soji Tottori University, Department of Microbiology and Pathology, Associate Professor, 医学部, 助教授 (60111126)
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| Co-Investigator(Kenkyū-buntansha) |
HIRAI Kazumitsu Tottori University, Department of Microbiology and Pathology, Professor, 医学部, 教授 (20093940)
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| Project Period (FY) |
2001 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2003: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2002: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2001: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | Spirometra erinaceieuropaei / Excretory / secretory products / macrophage / IP-10 / chemokine / gene expression / LPS / IFN-γ / INF-γ / TNF-α / NF-кB / MAPK |
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| Research Abstract |
Excretory/secretory (ES) products from Spirometra erinaceieuropaei plerocercoids suppressed the IP-10 gene expression, but not IRF-1, in macrophages stimulated with LPS or IFN-γ. IP-10 gene in LPS-stimulated macrophages will be induced by IFN-β through the MyD88 independent pathway, and ES products suppressed not only IFN-β gene expression but also IP-10, which was clarified by Northern blot analysis or RT-PCR. ES products suppressed the phosphorylation of STAT-1 Tyr701 in macrophages 3 h after the stimulation with LPS, but did not suppress the phosphorylation in the case of IFN-γ stimulation. The data of gel shift assay showed that the nuclear translocation and DNA binding activity of STAT-1 or ISGF3 did not change in macrophages stimulated with IFN-γ or IFN-β by the addition of ES products. Then, we examined the effects of ES products on the luciferase activities of macrophages transfected with luciferase vector containing -243 promoter or enhancer region of IP-10, which is the minimum response region. ES products suppressed the luciferase activities of macrophages stimulated with LPS and br IFN-γ. These data suggest that the suppressive mechanisms of IP-10 gene expression by ES products did not based on the inhibition of DNA binding activity of transcription factors such as STAT-1 and NF-κB, and originated from the conformation in IP-10 promoter. ES products also suppressed inducible nitric oxide synthase and the nitrite production, but ES products increased the CIITA and MHCII gene expression in the IFN-γ stimulated macrophages.
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