| Project/Area Number |
09470395
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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 |
Morphological basic dentistry
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| Research Institution | Showa University |
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Principal Investigator |
YAMAGUCHI Akira Showa University, School of Dentistry, Associate Professor, 歯学部, 助教授 (00142430)
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| Co-Investigator(Kenkyū-buntansha) |
KATAOKA Hiroko Showa University, School of Dentistry, Assistant, 歯学部, 助手 (60286846)
池田 通 昭和大学, 歯学部, 講師 (00211029)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥13,100,000 (Direct Cost: ¥13,100,000)
Fiscal Year 1998: ¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 1997: ¥9,000,000 (Direct Cost: ¥9,000,000)
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| Keywords | Bone Repair / BMP / Bone Formation / Osteoblast / 骨折 / 再生 / ヘッジホッグ |
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| Research Abstract |
Although bone is one of tissues with strong regenerating ability, molecular mechanism of bone repair has not been fully understood. In order to investigate molecular mechanism of bone repair by analysis of changes in gene expression during fracture healing, we conducted several experiments and obtained the following results.
We first examined expression of several mRNAs after fracture of mouse ribs by RT-PCR.Apparent mRNAs for Sonic hedgehog (Shh) and Indian hedgehog (Ihh) were not found in ribes before fracture. After 12-24 hours of fracture, we found substantial level of Shh mRNA.Its expression decreased after 48-72 hours of fracture. No Shh mRNA was found on day 5 after fracture. Expression for Ihh mRNA was found after 3 days of fracture. Expression of BMP-2 mRNA increased after 24-48 hours of fracture, while no apparent changes in expression of BMP-4 and BMP-7 mRNAs was found. These results indicated that Shh may play an important role in induction of BMP-2 at early phase of fracture repair. In addition, expression of mRNA for Cbfa1, which is an essential transcription factor of osteoblast differentiation and bone formation, increased after 72 hours of fracture. We are now investigating the expression pattern of these genes by in situ hybridization.
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