Identification of Helicobacter pylori-derived ncRNAs that induce host response disruption
Project/Area Number |
23659220
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Bacteriology (including Mycology)
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Research Institution | The University of Tokyo |
Principal Investigator |
MIMURO Hitomi 東京大学, 医科学研究所, 准教授 (80396887)
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Co-Investigator(Kenkyū-buntansha) |
MARUYAMA Fumito 東京医科歯科大学, 医歯(薬)学総合研究科, 准教授 (30423122)
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Project Period (FY) |
2011 – 2012
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Project Status |
Completed (Fiscal Year 2012)
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Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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Keywords | 細菌 / 感染症 / ヘリコバクターピロリ |
Research Abstract |
The aim of this study was to explore effector RNAs in Helicobacter pylori, which disrupt host responses. In silico analysis revealed that there is no effector RNAs possessing human microRNA-like conformation in H. pylori genome sequence. We found that the levels of several microRNAs were increased independent of the bacterial RNA transfer in H. pylori-infected epithelial cells. The effect of the identified microRNA increased in H. pylori-infected cells was estimated as the cell proliferation of host cells.
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Report
(3 results)
Research Products
(9 results)
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[Journal Article] Cell death and infection: a double-edged sword for host and pathogen survival.2011
Author(s)
Ashida, H., Mimuro, H., Ogawa, M., Kobayashi, T., Sanada, T., Kim, M. and Sasakawa, C.
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Journal Title
J Cell Biol
Volume: 195
Pages: 931-942
Related Report
Peer Reviewed
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