| Project/Area Number |
17390477
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Plastic surgery
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| Research Institution | Keio University |
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Principal Investigator |
KISHI Kazuo Keio University, Schcol af Medicine, Lecturer, 医学部, 講師 (40224919)
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| Co-Investigator(Kenkyū-buntansha) |
NAKAJIMA Tatsuo Keio University, School of Medicine, Professor, 医学部, 教授 (40095633)
KATSUBE Ken Tokyo Medical and Dental University, Graduate school of medicial ripnthl and pharmacology, lecturer, 大学院医歯学総合研究科, 講師 (20233760)
大原 博敏 慶應義塾大学, 医学部, 助手 (90338096)
清水 雄介 慶應義塾大学, 医学部, 助手 (10327570)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥15,500,000 (Direct Cost: ¥15,500,000)
Fiscal Year 2006: ¥7,500,000 (Direct Cost: ¥7,500,000)
Fiscal Year 2005: ¥8,000,000 (Direct Cost: ¥8,000,000)
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| Keywords | wound healing / skin / regeneration / fetal / 発生・分化 / マイクロアレイ / siRNA / 変換点 |
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| Research Abstract |
We could detect the differently expressed genes before and after the transition of mice fetal wound healing using microarray. By knocking down the genes from the fetal skin in vitro and in vivo, the function of these differently expressed genes were analysed. We also developed the in vitro and in vivo model using siRNA to knock down the expressing genes of fetuses. From our results using in vitro and in vivo models, genes that regulate regeneration were found to be twist 1 and fbn 1. Next we applied twist 1 and fbn 1 siRNA to the acute wounds of adult mice. The efficacy to the adult wounds was not clear.
Also, we knocked down these molecules using skin reconstruction models in the skin defects of scid mice. By knocking down twist 1 and shh, the epidermal wrinkle pattern was disrupted.
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