| Project/Area Number |
18591044
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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 |
Hematology
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| Research Institution | The University of Tokyo |
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Principal Investigator |
KUMANO Keiki The University of Tokyo, The University of TokyoHospital, Assistant Professor (90396721)
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| Project Period (FY) |
2006 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥4,010,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥510,000)
Fiscal Year 2007: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2006: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | Notch / Hematopoietic stem ce / niche / 血液内科 / 幹細胞 |
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| Research Abstract |
1) Estimation of hematopoietic stem cells (HSCs) in the reduced Notch signaling
We evaluated the HSCs of the Notch1+/-Notch2+/- mice or Notch1-/-Notch2-/- mice induced by the Mx1-cre transgene. Using FACS analysis, there was no difference in the number of CD34(-)KSL cells in the steady state or proliferative state induced by the 5-FU administration compared to the control mice.
In addition, we could not find the change of the number of HSCs by in vivo administration of g-secretase inhibitor (GSI), which is the inhibitor of Notch signaling. Quantification of HSCs was performed by the FACS analysis and transplantation.
2) The role of Notch signaling in the in vitro expansion of HSCs.
Inhibition of Notch signaling by GSI could impair the expansion of KSL cells, which include the HSCs, in the in vitro culture with FGF.
These results indicate that the dependency of HSCs to the Notch signaling differ between in vitro and in vivo.
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