| Project/Area Number |
20592334
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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 |
Surgical dentistry
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| Research Institution | Hiroshima University |
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Principal Investigator |
OKAMOTO Kosei Hiroshima University, 病院, 病院助教 (40423371)
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| Co-Investigator(Kenkyū-buntansha) |
KURIHARA Hidemi 広島大学, 大学院・医歯薬学総合研究科, 教授 (40161765)
OKAMOTO Tetuji 広島大学, 大学院・医歯薬学総合研究科, 教授 (00169153)
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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: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2009: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2008: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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| Keywords | 歯学 / 再生医学 |
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| Research Abstract |
I examined the no serum culture condition in serum-free medium hESF9 for embryonic stem cells. FGF -2, transforming growth factor-beta 1 and ascorbic acid were density-dependent and promoted the cell proliferation of the mesenchyma system stem cell (MSC). As a result of having weighed various gene expression between designated maintenance nutrient medium POWERDBY10 including the serum against the hESF10 nutrient medium which increased transforming growth factor-beta 1 in hESF9, Nanog which was the undifferentiated marker of the human embryonic stem cell, Oct3/4, the expression of Sox2 were higher in the hESF10 nutrient medium than POWERDBY10, and CD90 which was hMSC marker again, CD105, integrin β1 and typeIcollagen recognized overexpression. On the other hand, bone sialoprotein which was a bone differentiation marker, osteopontin, osteocalcin, the expression of osteonectin understood the thing that was lower than POWERDBY10. Based upon the foregoing, it was suggested that hESF10 promoted the increase of the hMSC cell which maintained an undifferentiation voltinism and many differentiation ability.
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