2010 Fiscal Year Final Research Report
Defense mechanisms of periapical inflammation by endothelial cells in persistent apical periodontitis
Project/Area Number |
20592240
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Conservative dentistry
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Research Institution | Nihon University |
Principal Investigator |
TAKEICHI Osamu Nihon University, 歯学部, 講師 (10277460)
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Project Period (FY) |
2008 – 2010
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Keywords | 慢性根尖性歯周炎 / 歯根肉芽種 / 歯根嚢胞 / 血管内皮細胞 / 一酸化窒素 / 糖化最終産物受容体 / midkine / ケモカイン |
Research Abstract |
To determine the mechanisms of persistent apical periodontitis, nitric oxide (NO), receptor for advanced glycation end products (RAGE) and midkine were analyzed using immunohistochemical and molecular biological techniques. NO and midkine were co-expressed by endothelial cells. RAGE was also expressed by AGE- expressing endothelial cells. In addition, co-expression of midkine and chemokines by endothelial cells were determined. The data suggested that endothelial cells could play a central role in extension and defense of periapical inflammation.
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[Presentation] Biocompatibility of novel vacuum sintered bodies of titanium medical apatite2008
Author(s)
Hayashi M, Ogata H, Suzuki N, Komori N, Takeichi O, Tamura K, Morisaki Y, Ogiso B, Fujita T
Organizer
86th General Session and Exhibition of the IADR
Place of Presentation
Toronto, ON, Canada
Year and Date
20080703-20080705
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[Remarks] ホームページ等