| Project/Area Number |
09557059
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
Circulatory organs internal medicine
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| Research Institution | The University of Tokyo |
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Principal Investigator |
MASUDA Michiaki The University of Tokyo, Graduate School of Medicine, Associate Professor, 大学院・医学系研究科, 助教授 (80199702)
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| Co-Investigator(Kenkyū-buntansha) |
SHINDO Takayuki The University of Tokyo Hospital, Clinical Fellow, 医学部・附属病院, 医員
KURIHARA Yukiko Organization for Pharmaceutical Safety and Research, Research Fellow, 研究員
OKAYAMA Minenobu DNA VEC Institute, Technical Research Fellow, 技術研究員
KURIHARA Hiroki The University of Tokyo Hospital, Assistant Professor, 医学部・附属病院, 助手 (20221947)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥11,800,000 (Direct Cost: ¥11,800,000)
Fiscal Year 1998: ¥5,500,000 (Direct Cost: ¥5,500,000)
Fiscal Year 1997: ¥6,300,000 (Direct Cost: ¥6,300,000)
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| Keywords | differentiation / endothelial cells / vascular smooth muscle cells / neural crest cells / viral vectors / gene transfer / endothelin / gene therapy / 神経提細胞 / 遺伝子治療 |
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| Research Abstract |
Masuda demonstrated that a neuropathogenic murine retrovirus PVC-211 transduced exogenous genes into rat endothelial cells more efficiently than other viruses and that treatment of the target endothelial cells with 2-deoxyglucose and vector inoculation in the absence of heparin further increased the transduction efficiency. In order to solve the problem that retrovirus-mediated gene transfer is irreversible, Masuda also developed two novel retroviral vectors, exploiting the Cre loxP homologous recombination system ; one is a "Flip-Flop" vector which enables reversible regulation of transduced genes by Cre-mediated DNA inversion, and the other is an excisable vector, which allows excision of transduced genes by Cre-mediated DNA deletion. The latter is useful for analyzing the host genome at proviral integration sites and mutagenic effects of proviral insertion.
Kurihara et al. established a system with which differentiation of primary neural crest cells derived from mouse embryos into vascular smooth muscle cells can be induced. Using this system, Kurihara et al. Demonstrated that colony formation of the smooth muscle cells require endothelin-1(ET-1)and that unlike BMP-2 and BMP-4, FGF-2 was inhibitory to differentiation of neural crest cells into smooth muscle cells. In addition, studies on ET-1 knockout mice suggested that ET- 1 might regulate differentiation of the vascular system through its effects on expression of a bHLH type DNA-binding protein, dHAND.
With this 2-year project, we were able to [1] establish and analyze the system for cardiovascular stem cell primary culture and differentiation induction and [2] develop vector systems for reversible gene transduction into cardiovascular cells. Based on these achievements, further studies will be carried out to establish cell lines, which retain the ability to differentiate into vascular smooth muscle cells, and generate animal models for gene therapy of cardiovascular diseases.
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