| Project/Area Number |
24592796
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Multi-year Fund |
|---|
| Section | 一般 |
|---|
| Research Field |
Functional basic dentistry
|
|---|
| Research Institution | Osaka University |
|---|
Principal Investigator |
KAWAI Shinji 大阪大学, 歯学研究科(研究院), 特任准教授 (40362678)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
AMANO Atsuo 大阪大学, 大学院歯学研究科, 教授 (50193024)
|
|---|
| Project Period (FY) |
2012-04-01 – 2015-03-31
|
| Project Status |
Completed (Fiscal Year 2014)
|
| Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
|---|
| Keywords | 骨芽細胞 / 転写因子 / 骨形成 / 特異的細胞破壊 |
|---|
| Outline of Final Research Achievements |
We aimed to clarify the relationship between Osr2 expressing cells and osteoblast/odontoblast/synovial cells in the present research. We planned that cell disruption of Osr2 expressing cells by Cre-loxP with diphtheria toxin. We scheduled to analyze long bone and skull bone from the postnatal mice and to stain the section of bones by HE, MacNeal, or Goldner staining. Unfortunately, our purpose mice died during embryogenesis. Embryonic lethality was happened in early development of the mice. The reason of embryonic lethal seems to be the expression of Osr2 in various types of organs such as intestine, kidney, pituitary gland, lung, and stomach.
|
