Nitric oxide inhibits HIV-1 replication in human astrocytoma cells

被引:22
作者
Persichini, T
Colasanti, M
Fraziano, M
Colizzi, V
Ascenzi, P
Lauro, GM
机构
[1] Univ Rome Tre, Dept Biol, I-00146 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
关键词
nitric oxide; HIV-1; replication; AIDS dementia complex; glial cells;
D O I
10.1006/bbrc.1998.9880
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Astroglial cells represent a target for HIV infection in the central nervous system. In astrocytes, HIV infection is poorly productive, being characterized by a persistent state of viral latency. However, activation of the nuclear factor NF-kappa B and its binding to HIV long terminal repeat (LTR) can induce HIV replication. Moreover, nitric oxide (NO) can affect NF-kappa B activation in glial cells. Therefore, we hypothesize that NO may reduce HIV replication in human astroglial cells by inhibiting HIV-1 LTR transcriptional activity. In this respect, we show that NO donors reduce viral replication in HIV-l-infected human astrocytoma T67 cells, taken as an astroglial model, Furthermore, using transfected T67 cells, we demonstrate that NO donors inhibit HIV-1 LTR transcriptional activity. These results suggest that the use of NO-releasing drugs may represent a potential, novel approach in inhibiting HIV replication in the central nervous system. (C) 1999 Academic Press.
引用
收藏
页码:200 / 202
页数:3
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