1995 Fiscal Year Final Research Report Summary
A study on expression and function of bone morphogenetic protein during maxillofacial development
Project/Area Number |
06671993
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Research Category |
Grant-in-Aid for General Scientific Research (C)
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Allocation Type | Single-year Grants |
Research Field |
Surgical dentistry
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Research Institution | Tokyo Medical and Dental University |
Principal Investigator |
IWAKI Hiroshi Tokyo Med.and Dent.Univ., Dentistry, assistant professor, 歯学部, 講師 (70107308)
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Co-Investigator(Kenkyū-buntansha) |
OIDA Shinichiro Tokyo Med.and Dent.Univ., Dentistry, assistant professor, 歯学部, 助手 (10114745)
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Project Period (FY) |
1994 – 1995
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Keywords | BMP / BMP receptor / TGF-beta / activin |
Research Abstract |
Bone Morphogenetic Protein (BMP), which belongs to the transforming growth factor-beta (TGF-beta) superfamily, was originally identified in the extract from bone by its capacity to induce ectopic bone formation. Recent studies have revealed that BMPs are involved in maxillofacial development. In order to investigate the precise molecular mechanism of BMPs in maxillofacial development, we performed the following studies. Dental pulp has a potential to induce ectopic bone formation. We thought that bone morphogenetic proteins (BMPs) are involved in the osteoinductive activity of dental pulp. In order to prove this assumption, we constructed a cDNA library from primary culture cells of human dental pulp (HDP cells). Three distinct cDNA clones encoding human BMP-2, -4, -6 were isolated. To elucidate the receptor system of BMP,we performed molecular clonning of rat BMP receptor. PCR-based analysis revealed that mRNA for BMP receptors were expressed in the BMP-induced bone forming tissues throughout the stages tested and that mRNA for activin receptor was also expressed. These results suggest that these receptors play imporatant roles for the ectopic bone formation induced by BMP.In addition, expression of mRNAs for TGB-beta receptors and activin receptors was also detected in the BMP-implanted tissues, which suggested the possible involvement of TGF-betas and activins as ligands in the ectopic bone formation.
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