| Project/Area Number |
10357020
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
Periodontal dentistry
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| Research Institution | Hiroshima University |
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Principal Investigator |
KURIHARA Hidemi Hiroshima Univ., Faculty of Dentistry, Professor, 歯学部, 教授 (40161765)
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| Co-Investigator(Kenkyū-buntansha) |
SUGAI Motoyuki Hiroshima Univ., Faculty of Dentistry, Professor, 歯学部, 教授 (10201568)
OKADA Hiroshi Ohsaka Univ., Faculty of Dentistry, Professor, 歯学部, 教授 (40038865)
ABIKO Yoshimitsu Nihon Univ., School of Dentistry at Matsudo, Professor, 松戸歯学部, 教授 (70050086)
YAMAZAKI Kazuhisa Hiroshima Univ., Faculty of Dentistry, Professor, 歯学部, 講師 (00182478)
TAKASHIBA Shogo Okayama Univ., Dental School, Associate Professor, 歯学部, 助教授 (50226768)
安孫子 宜光 (庄司 茂) 日本大学, 松戸歯学部, 教授 (10142986)
片岡 正俊 徳島大学, 歯学部, 助手 (20224438)
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| Project Period (FY) |
1998 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥25,300,000 (Direct Cost: ¥25,300,000)
Fiscal Year 1999: ¥15,100,000 (Direct Cost: ¥15,100,000)
Fiscal Year 1998: ¥10,200,000 (Direct Cost: ¥10,200,000)
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| Keywords | genetic diagnosis / Porphyromonas gingivalis / IL-1 / autoantibody / HLA class II / cytolethal distending toxin / hypophosphatasia / CDR3 / Porphyromonas gingivalis / 低フォスファターゼ症 / 歯周病 / 遺伝子 / 発症 / 歯周病感受性 / 歯周病関連菌 |
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| Research Abstract |
In this project, we evaluate the genes related periodontal disease from the diversified aspects, infected bacteria, host defense system, tissue metabolism, and tissue regeneration. Analysis of DNA sequence of hemagglutinin from Porphyromonas gingivalis revealed its functional domain. The binding domain contains the specific sequence, PVQNT, similar to influenza virus. A novel gene (Aa cdt) encoding cytolethal distending toxin (CDT) was successfully cloned from Actinobacillus actinomycetemcomitans. Aa cdt was composed with three clusters, and each cluster was encoding CDT-A, -B, and -C. CDT-A, -B and -C were essential for expressing CDT activity.
The genes related autoantibody production in patients with periodontitis were evaluated on T cell receptor (TCR) and human leukocyte antigen (HLA). The peripheral T cells were stimulated by hrHSP60 or P. gingivalis GroEL and DNA sequence of CDR3 region of their TCR β-chain. The amino-acid sequenee of CDR3 was the same between the expanded T cell
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clone and the accumulated T cell clone in inflamed gingival tissue. The HLA class II genotypes of patients with periodontitis, autoantibody production and PVB 19 infection were analyzed by PCR-RFLP. The frequencies of DQA1 *0101, DQA1 *0501, and DQB1*0503 in patients with periodontitis, autoantibody production and PVB 19 infection were higher than in other patients and healthy subjects. The relationship between IL-1 genotypes and prevalence of adult periodontitis was reported in the United State, however we could not found this relationship in Japanese.
Two patients with hypophosphatasia, usually accompanied with periodontitis, and their family members were analyzed to detect mutation on tissue-nonspecifie alkaline phosphatase gene. Novel three point mutations on the alkaline phosphatase gene were revealed
Novel genes related periodontal tissue regeneration were found by the subtraction method between wound periodontal tissue under tissue repair and healthy periodontal tissue. Sixteen novel cDNAS in enhanced expression genes and 9 novel cDNAS in depressed expression genes were successfully cloned. Less
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