2002 Fiscal Year Final Research Report Summary
The molecular analysis of laser irradiation effect for the osteoblast
| Project/Area Number |
13672176
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
矯正・小児・社会系歯学
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| Research Institution | Kanagawa Dental College |
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Principal Investigator |
SASAGURI Kenichi Kanagawa Dental College, Dept. of Orthodontics, Lecturer, 歯学部, 講師 (10235286)
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| Co-Investigator(Kenkyū-buntansha) |
SHIMONO Masaki Tokyo Dental College, Dept. of Pathology, Professor, 歯学部, 教授 (00085771)
ISHIKAWA Tatsuya Tokyo Dental College, Dept. of Operative Dentistry, Professor, 歯学部, 教授 (30085708)
SATO Sadao Kanagawa Dental College, Dept. of Orthodontics, Professor, 歯学部, 教授 (00084799)
MATSUZAKA Kenichi Tokyo Dental College, Dept. of clinical Pathophysiology, Lecturer, 歯学部, 講師 (70266568)
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| Project Period (FY) |
2001 – 2002
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| Keywords | Osteoblast / cbfal |
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| Research Abstract |
The study was investigated that what kind of effect the laser irradiation causes the human osteoblasts cell line, NHOst cell (Bio Whittaker Co.), in vitro. As a reason using the NHOst cell, it is for examining for the purpose of always feeding back the result for the daily clinic, such as regeneration of oral hard tissues and implantation. However, this cell showed morphology of dedifferentiating by the subculture of 2〜3 times, and alkaline phosphatase activity which was an index to the differentiation of osteoblast and DNA content which are an index to cell proliferation did not become constant. Then, the experiment should be carried out using MG63 cell that it is the human osteosarcoma cell line. It is reported that MG63 cell is efficiently differentiated an osteoblast like cell by the addition of active vitamin D_3, and we have been confirmed that this applicant has also expressed osteocalcin gene by the polymerase chain reaction (PCR). In the future, it will be examined that the effects of laser irradiation investigate on the osteoblast like cell, MG63.
In the meantime, We have raised monoclonal antibody against recombinant murine cbfa1 and cbfβ protein. The specificity of these antibodies were characterized by its reaction in Western blot analysis and electrophoretic mobility shift assay (EMSA) on mourine cells and tissues. In the future, the specificity of the antibody is examined using MG63 cell and human hard tissues.
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