A study of osteoblast differentiation and activation in Msx2 gene-transfer ES/iPS cells.
| Project/Area Number |
23792438
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Orthodontic/Pediatric dentistry
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| Research Institution | Kagoshima University |
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Principal Investigator |
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| Research Collaborator |
MITSUI Kaoru 鹿児島大学, 医歯学総合研究科, 講師 (40324975)
KOSAI Ken-ichiro 鹿児島大学, 医歯学総合研究科, 教授 (90258418)
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| Project Period (FY) |
2011 – 2013
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2013: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2012: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2011: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | 骨芽細胞 / 細胞分化 / 分化・機能活性 |
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| Research Abstract |
There have been no clear reports so far that Msx2 gene take part in the mechanism of osteoblast differentiation, which is responsible for the bone remodeling and regeneration in orthodontic treatments. The purpose of this study, therefore, was to investigate the roles of Msx2 in osteoblast differentiation and osteogenesis with mouse Embryonic Stem (ES) cells and Induced Pluripotent Stem (iPS) cells. ES cells and iPS cells which transfected with Msx2 gene were cocultured with feeder cells, and mRNA levels of osteoblastic phenotype and alkaline phosphatase activity were determined for cell differentiation and activation. The value of bone nodules was also determined for mineralization. As a result, it was suggested that Msx2 play a key role in controlling osteoblast differentiation from ES/iPS cells.
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Report
(4 results)
Research Products
(4 results)
