| Project/Area Number |
07457585
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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 |
Experimental pathology
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| Research Institution | Osaka University |
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Principal Investigator |
NOMURA Shintaro Osaka University Medical School Associate Professor, 医学部, 助教授 (80159087)
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| Co-Investigator(Kenkyū-buntansha) |
HIROTA Seiichi Osaka University Medical School Assistant Professor, 医学部, 助手 (50218856)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1996: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | fracture lrealing / osteopontin / osteosarcoma / osteoblast / transcription factor / calcification / chondrocyte / scurvy / オステオカルシン / オステオネクチン / ビタミンC / 骨折 / 内軟骨性骨化 / 膜性骨化 / コラーゲン / 遺伝子発現 / 骨形成不全 / 仮骨 / 炎症 / 偽関節 |
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| Research Abstract |
Impaired fracture healing process was investigated by molecular histological techniques such as in situ hybridization. ODS (Osteogenesis Disorder Shionogi) rat was used for Scurvy model. Membranous ossification process in fracture healing was strongly inhibited by the depletion of vitamin C.Particularly, no expression of osteopontin, extracellular matrix protein located in the bone matrix, was detected. Early stages of endochondral ossification was not strongly inhibited. The unmber of chondrocytes in vitamin C depleted rats was comparable to that of normal rat. However, only a few number of hypertrophic chondrocytes which express osteopontin nRNA was observed. The results suggest the possibility that due to the impaired expression of osteopontin, calcification process in the scurvy was strongly inhibited. Furthermore, transcriptional factors regulating the expression of osteopontin gene was identified in vivo and in vitro. CBFA1, PU.1, MITF were cooperatively interacted with 5'-flanking region of osteopontin gene. No expression of osteopontin gene was detected in the knockout mice of cbfa-1 gene. This knockout mice showed almost no calcification in the bone tissue. The result also suggested the involvement of osteopontin to the calcification process. The biological role of osteopontin for the bone remodeling was also investigated. Enhanced expression of osteopnotin gene was observed by mechanical stress of "press" in the osteocytes. The result indicated that the osteocytes acted as sensory cells respond to echanical stress by espressing osteopontin gene.
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