| Project/Area Number |
61570226
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Virology
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| Research Institution | Cancer Research Institute, Kanazawa University |
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Principal Investigator |
TANAKA Junji Cancer Research Institute, Kanazawa University, ガン研究所, 助教授 (60019875)
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| Project Period (FY) |
1986 – 1987
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| Project Status |
Completed (Fiscal Year 1987)
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| Budget Amount *help |
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1987: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1986: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | human cytomegalovirus / latent infection / persistent infection / in vitro model system / 再活性化 / ヒトサイトメガロウィルス / 試験管内モデルシステム |
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| Research Abstract |
Human cytomegalovirus (HCMV) is capable of establishing both persistent and latent infections after a primary infection in vivo. For study of the mechanisms of HCMV latent and persistent infections in vivo, I have attempted to establish and characterize an in vitro HCMV latency and persistence model system using human cell cultures. When a human thyroid papillary carcinoma cell line (TPC-1) was infected with HCMV and incubated at 37 or 40.5 , persistently or latently infected cultures could be established, respectively. The virus latent and persistent states were reversible by shifting the incubation temperature. Although HCMV-specific immediate early proteins and antigens were detectable during the latent period, a detectable level of virus-specified DNA polymerase was not induced, suggesting that the blockage of HCMV replication in the latently infected cultures occurs at the early stages of the HCMV replicatin cycle. The latently infected cells were shown to be susceptible to superinfection with homologous and heterologous strains of HCMV and to be resistance to complement-mediated immune cytolysis. The latent HCMV was reactivated by reducing the incubation temperature from 40.5 to 37 . However, when the latently infected cultures were treated with inhibitors of prostaglandin synthesis (indomethacin and tetracatine) immediately after being shifted to 37 , reactivation of the latent virus was not observed.
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