| Project/Area Number |
12557028
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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 |
Virology
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| Research Institution | Hokkaido University |
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Principal Investigator |
TAKADA Kenzo Hokkaido Univ., Institute for Genetic Medicine, Prof., 遺伝子病制御研究所, 教授 (30133721)
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| Co-Investigator(Kenkyū-buntansha) |
MARUO Seiji Hokkaido Univ., Institute for Genetic Medicine, Inst., 遺伝子病制御研究所, 助手 (70292018)
IWAKIRI Dai Hokkaido Univ., Institute for Genetic Medicine, Inst., 遺伝子病制御研究所, 助手 (10307853)
KANNO Hiroyuki Hokkaido Univ., Institute for Genetic Medicine, Asso.Prof., 遺伝子病制御研究所, 助教授 (40252663)
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| Project Period (FY) |
2000 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥13,200,000 (Direct Cost: ¥13,200,000)
Fiscal Year 2001: ¥5,200,000 (Direct Cost: ¥5,200,000)
Fiscal Year 2000: ¥8,000,000 (Direct Cost: ¥8,000,000)
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| Keywords | Epstein-Barr virus / transgenic rat / CD21 / model animal / receptor / EBウイルス / 動物モデル / クラスII |
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| Research Abstract |
The human CD21 (hCD21) molecule, which is preferentially expressed on B-lymphocytes, is the receptor for EBV adsorption, and this determines the predominant B-lymphocyte tropism of EBV. B-lymphocytes from humans and some primates, but not from other species, are susceptible to EBV infection. We have recently demonstrated that introduction of the hCD21 gene makes some canine and rat cells susceptible to EBV infection and stably EBV-infected cell clones could be isolated from these cells. These results suggest that once the initial barrier to attachment is overcome, EBV can penetrate into and stably infect canine and rat cells. This finding has prompted us to generate a transgenic rat with the hCD21 gene, which could become an animal model for EBV infection. We generated transgenic rats expressing the human CD21 gene (hCD21) driven by the mouse immunoglobulin enhancer. Spleen B-lymphocytes expressing hCD21 were susceptible to Epstein-Barr virus (EBV) infection as evidenced by EBV latent gene expression, but the infection was abortive and was not followed by blastogenesis, cellular DNA synthesis or proliferation. The present findings indicate that human and rat lymphocytes respond to EBV infection differently in vitro. We are now studying whether the hCD21 transgenic rat could become a model animal for EBV infection.
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