Establishment of the neurocristopathy treatment model and analysis of the differentiation mechanism of neural crest cells using mouse embryonic stem cells.
| Project/Area Number |
20592086
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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 |
Pediatric surgery
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| Research Institution | Gifu University |
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Principal Investigator |
MOTOHASHI Tsutomu Gifu University, 医学系研究科, 講師 (40334932)
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| Project Period (FY) |
2008 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2010: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2009: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2008: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 神経堤細胞 / ES細胞 / 神経堤症 / 転写因子Sox10 / 遺伝子改変マウス / セルソーター |
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| Research Abstract |
For the purpose of elucidating the mechanism of the neural crest cell differentiation, we generated the embryonic stem cells and mice, where the expression of Sox10 can be visualized with a fluorescent protein. The transplanted neural crest cells derived from the ES cells survived in the embryonic intestinal tract. We separated neural crest cells from the gene modified embryo and analyzed the gene expression by gene arrays. In addition, using the mice, we found that the multipotent neural crest-like cells were maintained in skin.
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Report
(4 results)
Research Products
(24 results)
