| Project/Area Number |
14F04720
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| Research Category |
Grant-in-Aid for JSPS Fellows
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| Allocation Type | Single-year Grants |
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| Section | 外国 |
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| Research Field |
Nanobioscience
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| Research Institution | The University of Tokyo |
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Principal Investigator |
松永 行子 (津田行子 / 松永 行子(津田行子)) 東京大学, 生産技術研究所, 講師 (00533663)
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| Co-Investigator(Kenkyū-buntansha) |
TAN ANGEL 東京大学, 生産技術研究所, 外国人特別研究員
TAN Angel 東京大学, 生産技術研究所, 外国人特別研究員
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| Project Period (FY) |
2014-04-25 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 2015: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2014: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | 3D artery tissues / smooth muscle cells / endothelial cells / co-culture / collagen microchannel / inflammation / monocytes / lipids / vascular tissue |
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| Outline of Annual Research Achievements |
AIMS: This two-year JSPS postdoctoral fellowship (FY2014-2016) aims at fabricating a three-dimensional (3D) co-culture artery-on-a-chip to closely simulate the human vascular morphology, both in the healthy and inflammatory disease conditions. The longer-term goal of this project is to develop viable in vitro tools to support high-throughput therapeutic and biopharmaceutical research of various drugs and pharmaceutical formulated compounds.
PROGRESS: To date, we have established two simple needle-based fabrication procedures to achieve controllable arterial architectures on a microchip; (a) an arteriole-like bilayer of human vascular smooth muscle cells (SMC) and endothelial cells (EC), and (b) an artery-like structure composed of multilayers of SMC covered by an inner EC monolayer lining. These proof-of-concept microvascular models have been extensively validated for their robustness and reproducibility, as well as for physical stability and metabolic behaviors to mimic the healthy state of a blood vessel. Meanwhile, experiments are ongoing to incorporate various pathological factors into these artery-like tissues to induce vascular inflammatory disease.
OUTCOME; The results obtained have formed the basis for a manuscript, which is near to submission (by April 2016) as a full length paper to an international tissue engineering journal. It also contributes to a poster presentation at the University of Tokyo Life Science Symposium (第16回東大生命科学シンポジウム) on April 23, 2016.
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| Research Progress Status |
27年度が最終年度であるため、記入しない。
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| Strategy for Future Research Activity |
27年度が最終年度であるため、記入しない。
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