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- W1967967941 abstract "Nitric oxide (NO), a mediator of biological functions, has an antimicrobial activity against a variety of pathogens including viruses. In this study, we found that a constitutive, low level of inducible NO synthase (iNOS) mRNA was expressed in the EBV-infected gastric tissue-derived GT38 and GT39 cell lines, by analysis with the reverse transcription–polymerase chain reaction (RT–PCR) and Southern blotting. Treatment of these cells with a specific NOS inhibitor, NG-monomethyl-l-arginine (l-NMMA), induced the immediate-early, EBV transactivator gene BZLF1 protein ZEBRA, suggesting a significant increase in EBV reactivation by l-NMMA. Northern blotting demonstrated that BZLF1 and BRLF1 transcripts were also induced by 12-O-tetradecanoylphorbol-13 acetate (TPA). Meanwhile, constitutive expression of iNOS mRNA was inhibited by TPA. l-NMMA also enhanced TPA-induced expression of the BZLF1 gene. On the other hand, a NO donor, S-nitroso-N-acetylpenicillamine (SNAP), which releases NO in an aqueous solution, inhibited the TPA-induced BZLF1 gene expression in a dose-dependent manner at both mRNA and protein levels. These results demonstrated that NO is a regulatory factor in maintaining virus latency via inhibiting EBV reactivation in the infected epithelial cells." @default.
- W1967967941 created "2016-06-24" @default.
- W1967967941 creator A5062020822 @default.
- W1967967941 creator A5079563421 @default.
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- W1967967941 date "1999-06-01" @default.
- W1967967941 modified "2023-09-27" @default.
- W1967967941 title "Nitric Oxide Down-Regulates Epstein–Barr Virus Reactivation in Epithelial Cell Lines" @default.
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- W1967967941 doi "https://doi.org/10.1006/viro.1999.9748" @default.
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