Examination of the gene therapy for OME using Decoy oligo.
| Project/Area Number |
15591823
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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 |
Otorhinolaryngology
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| Research Institution | Kagoshima University |
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Principal Investigator |
MATSUNE Shoji (2005) Kagoshima University, Graduate School of Medical and Dental Sciences, Associate Professor, 大学院医歯学総合研究科, 助教授 (00253899)
牛飼 雅人 (2003-2004) 鹿児島大学, 医学部・歯学部附属病院, 講師 (00284886)
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| Co-Investigator(Kenkyū-buntansha) |
KURONO Yuichi Kagoshima University, Graduate School of Medical and Dental Sciences, Professor, 大学院医歯学総合研究科, 教授 (80153427)
SAGARA Yukari Kagoshima University, Graduate School of Medical and Dental Sciences, Research Associate, 大学院医歯学総合研究科, 助手 (90347112)
HAYASHI Tamon University Hospital, Faculty of Medicine and Dentistry, Research Associate, 医学部・歯学部附属病院, 助手 (50381158)
YOSHIFUKU Kousuke University Hospital, Faculty of Medicine and Dentistry, resident, 医学部・歯学部附属病院, 医員 (70381168)
松根 彰志 鹿児島大学, 大学院・医歯学総合研究科, 助教授 (00253899)
宮之原 郁代 鹿児島大学, 医学部・歯学部附属病院, 講師 (40305131)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2005: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2004: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2003: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | NF-κB / Decoy Oligo / gene therapy / OME / sinusitis / NF-κBデコイ / センダイウイルス / アデノイド線維芽細胞 / デコイ / マウス / 炎症性サイトカイン / NF-kB |
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| Research Abstract |
TNF-a induced or upregulated IL-8 production in adenoidal fibroblasts. IL-8 level in epipharyngeal effusion and the compliance of tympanic membrane was showed clinically to be correlated in OME, suggesting that I L-8 production from adenoidal fibroblasts is one of the important causative factors of OME. Additionally, VCAM-1 was induced by the stimulation of TNF-a and/or IL-4 in nasal fibroblasts.
Translocation of NF-κB is the essential step both in IL-8 production in adenoidal fibroblasts and VCAM-1 production from nasal fibroblasts.
Based on these data, NF-κ B is the key factor and the regulation of this step seems to be a new strategy to treat OME and C S.
In this project, NF-κB Decoy oligo was expected to suppress the activation of NF-IC B translocation. We applied the liposome method and sendai virus vector to transfect NF-κ B Decoy oligo to cultured fibroblast. However, the transfection was not successful and we could not go to the step of the application of this strategy to the OME mouse model.
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Report
(4 results)
Research Products
(8 results)
