| Project/Area Number |
09671254
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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 |
General surgery
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| Research Institution | Tokai University |
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Principal Investigator |
KATAYAMA Tokitaka Tokai University, School of Medicine, Assistant Professor, 医学部, 助手 (40214332)
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| Co-Investigator(Kenkyū-buntansha) |
UEYAMA Yoshito Tokai University, School of Medicine, Associate Professor, 医学部, 助教授 (30072408)
INOKUCHI Sadaki Tokai University, School of Medicine, Associate Professor, 医学部, 助教授 (60160008)
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| Project Period (FY) |
1997 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 1999: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1998: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1997: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | Primary culture / Human hepatocytes / Adenovirus vector / Immortalization / SV40T antigen / Hybrid artificial liver / 初代培養用細胞 / 遺伝子導入 / 形質転換コロニー / 初代培養肝細胞 |
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| Research Abstract |
Use of primary culture of hepatocytes in developing hybrid artificial liver is a topic of active research. However, primary cultures of hepatocytes remain viable for only a few weeks under normal cultivation conditions. By using adenovirus vector and introducing SV40 primary gene into rat and marmoset primary cultures of hepatocytes. I have succeeded in transformed conversion resulting in longer cultivation period, immortalization, and massive cultivation. By using the same technique, I have attempted to produce hybrid artificial liver by using human hepatocytes.
Methods and Results: 1. Adenovirus vector produced by recombination of E1A and E1B genes in human adenovirus with multiple deletion SV40 primary genes, was added to human primary cultures of hepatocytes by MOI (multiplicity of infection) and cultivated under 37℃ for two hours, then fixed in ethanol after 48 hours of additional cultivation, and immunostained by using antibody to SV40T antigen. Rate of T antigen positive was appr
… More
oximately 20% in MOI 100, 4% in MOI 10, less than 0.5% in MOI 1, and these results were depend on MOI.
2. Adenovirus vector was introduced in human hepatocytes in MOI 100 and plated to 1xl0ィイD16ィエD1 flask(25 cmィイD13ィエD1). After 3-4 weeks, approximately 100/colonies undergoing transformed conversion were produced from 10 cells.
3. Human hepatocytes introducing with primary SV40 genes were cultivated as a bulk for longer than 12 months and the cells mostly SV40T antigen positive, continued to reproducefavorably and attained immortalization. Also immunostaining with albumin was localization in cytosol of these cells.
Conclusion: By using adenovirus vector efficient introduction of SV40 primary gene and transformed conversion was possible resulting in massive cultivation and immortalization.
Discussion: Under the single layer cultivation method employed this time, hepatocyte function was found to deterorated with time by measuring urea production and tyrosine amino transferase (TAT) activity. I plan to used third degree high dense cultivation to improve this aspect in the future. Less
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