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(Received for publication, May 6, 1996)
From the Department of Biochemical Genetics, Medical Research
Institute, Tokyo Medical and Dental University, Yushima,
Bunkyo-ku, Tokyo 113, Japan
Human lymphoid cell lines were transfected with
HIV-1-LTR-CAT DNA and permanently transformed cell lines were obtained.
These transformed cell lines were treated with 0.01 mM
H2O2 for 25 days and the chloramphenicol
acetyltransferase (CAT) activities of these cell lines were measured.
The CAT activities of transformed cell lines were latent in normal
culture conditions, but were activated by retreatment with 0.2 mM H2O2 for 1 h. On treatment
with 0.05 mM H2O2 for 1 h, the
CAT activity of these cell lines maintained in normal conditions
remained latent, whereas cell lines pretreated with 0.01 mM
H2O2 for 25 days were greatly activated by this
treatment. Here, the HIV-1 promoter seemed latent in normal culture
conditions, but it could be activated by a comparatively low
concentration (0.05 mM) of H2O2
after treatment with a dilute H2O2 (0.01 mM) for about 1 month. Many patients infected with human
immunodeficiency virus 1 (HIV-1) show a long latent period before
development of AIDS. During this latent period, their infected cells
may be subjected to oxidative stress due to metabolism and physical
movement. The present results indicate that oxidative stress may cause
activation of the HIV-1 promoter in patients with latent HIV-1.
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