Project/Area Number |
13308055
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Research Category |
Grant-in-Aid for Scientific Research (A)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Biomedical engineering/Biological material science
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Research Institution | Tokyo Women's Medical University |
Principal Investigator |
OKANO Teruo Tokyo Women's Medical University, Department of Medicine, Professor, 医学部, 教授 (00130237)
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Co-Investigator(Kenkyū-buntansha) |
YAMATO Masayuki Tokyo Women's Medical University, Department of Medicine, Associate Professor, 医学部, 助教授 (40267117)
KIKUCHI Akihiko Tokyo Women's Medical University, Department of Medicine, Associate Professor, 医学部, 助教授 (40266820)
YOKOYAMA Masayuki Tokyo Women's Medical University, Department of Medicine, Associate Professor, 医学部, 助教授 (20220577)
AKIYAMA Yoshikatsu Tokyo Women's Medical University, Department of Medicine, Research Assistant Professor, 医学部, 助手 (20349640)
SHIMIZU Tatsuya Tokyo Women's Medical University, Department of Medicine, Assistant Professor, 医学部, 講師 (40318100)
KUSHIDA Ai Tokyo Women's Medical University, Department of Medicine, Research Assistant Professor (10338981)
青柳 隆夫 東京女子医科大学, 医学部, 助教授 (40277132)
|
Project Period (FY) |
2001 – 2003
|
Project Status |
Completed (Fiscal Year 2003)
|
Budget Amount *help |
¥53,040,000 (Direct Cost: ¥40,800,000、Indirect Cost: ¥12,240,000)
Fiscal Year 2003: ¥12,350,000 (Direct Cost: ¥9,500,000、Indirect Cost: ¥2,850,000)
Fiscal Year 2002: ¥13,390,000 (Direct Cost: ¥10,300,000、Indirect Cost: ¥3,090,000)
Fiscal Year 2001: ¥27,300,000 (Direct Cost: ¥21,000,000、Indirect Cost: ¥6,300,000)
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Keywords | poly(N-isopropylacrylamide) / patterned thermoresponsive surfaces / pattern co-culture / parenchymal cells / endothelial cells / albumin production / urea synthesis / patterned domain sizes / 温度応答性表面 / 細胞シートのマニピュレーション / 相転移挙動 |
Research Abstract |
This research focused on the design and characterization of novel patterned dual thermoresponsive surfaces for possible patterned co-culture and recovery of co-cultured cell monolayers by temperature modulation. Thermoresponsive polymers of poly(N-isopropylacrylamide) and its hydrophobic derivatives containing n-butyl methacrylate (BMA) as hydrophobic units were pattern grafted using electron beam irradiated polymerization. In this fiscal year, several types of the patterned dual thermoresponsive surfaces were prepared by applying limited electron beam irradiated polymerization of BMA onto PIPAAm-grafted surfaces through aluminum masks having different sizes of circular holes. In case of the 100μmφ-patterned masks, irradiated electron beam was diffracted with the mask and meniscus of the monomer solution, resulting in the formation of hydrophobic patterns with >100μmφ in size, and we did not obtain patterned dual thermoresponsive surfaces reproducibly. Using metal masks with larger pat
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tern sizes (0.5mmφ and 1.0mmφ), we successfully prepared patterned, dual thermoresponsive surfaces. Patterned co-culture of hepatocytes (HCs) and endothelial cells (ECs) were then performed by modulation of surface hydrophilic/hydrophobic property alteration with temperature. HCs were seeded and cultured at 27℃ to culture only onto relatively hydrophobic domains, followed by ECs culture at 37℃ to realize patterned co-culture of these two cell types. By lowering culture temperature to 20℃ at which entire surfaces become hydrophilic, co-cultured cells spontaneously detach from the culture surfaces in a single cell sheet maintaining patterned structure. We then investigate the effect of the pattern sizes on hepatic function changes in patterned co-culture systems, in terms of the albumin production and urea syntheses by ammonium metabolism. Both physiological functions increased with decreasing patterned domain sizes at constant HCs/ECs ratio than homotypic culture of HCs. More functional augmentation was observed with smaller patterned domains with longer culture periods. These results are consistent with the previously obtained results, in which HC monolayers were covered with EC monolayers obtained by using PIPAAm-grafted dishes. Thus, the control of the distance between HCs and ECs has preferential influences to co-cultured cell functionalities including cellular viabilities. Less
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