Identification and mechanical analysis of the functional lncRNA in pro-inflammatory macrophages
| Project/Area Number |
26860544
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Cardiovascular medicine
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| Research Institution | The University of Tokyo |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
MANABE Ichiro 千葉大学, 大学院医学研究院長寿医学講座, 教授 (70359628)
FUJIU Katsuhito 東京大学, 医学部附属病院, 特任助教 (30422306)
KOMURO Issei 東京大学, 大学院医学系研究科器官病態内科学講座循環器内科学, 教授 (30260483)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | マクロファージ / ノンコーディングRNA / 慢性炎症 |
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| Outline of Final Research Achievements |
Macrophages play pivotal roles in metabolic syndrome and atherosclerosis, fluctuating the function dynamically. The molecular mechanism of the regulation remains to be completely elucidated. In this study I identified a functional long noncoding RNA (lncRNA), named lncFAO, which is implicated in regulation of pro-inflammatory cytokine expression in macrophages. Functional lncRNAs have function via their own steric structure by themselves. I revealed that lncFAO regulates macrophage phenotypes by binding with lipid metabolic enzyme. I think that this study showed a novel mechanism which regulate macrophage in chronic inflammatory diseases, and pave a pathway to identifications of new therapeutic targets.
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Report
(3 results)
Research Products
(8 results)
