μ-opioid modulation of HIV-1 coreceptor expression and HIV-1 replication

被引:126
|
作者
Steele, AD
Henderson, EE
Rogers, TJ
机构
[1] Temple Univ, Sch Med, Dept Microbiol & Immunol, Ctr Substance Abuse Res, Philadelphia, PA 19140 USA
[2] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Ctr Substance Abuse Res, Philadelphia, PA 19140 USA
关键词
opioids; chemokine receptors; HIV;
D O I
10.1016/S0042-6822(03)00015-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A substantial proportion of HIV-1-infected individuals are intravenous drug users (IVDUs) who abuse opiates. Opioids induce a number of immunomodulatory effects that may directly influence HIV-1 disease progression. In the present report, we have investigated the effect of opioids on the expression of the major HIV-1 coreceptors CXCR4 and CCR5. For these studies we have focused on opiates which are ligands for the mu-opioid receptor. Our results show that DAMGO, a selective mu-opioid agonist, increases CXCR4 and CCR5 expression in both CD3' lymphoblasts and CD14(+) monocytes three- to fivefold. Furthermore, DAMGO-induced elevation of HIV-1 coreceptor expression translates into enhanced replication of both X4 and R5 viral strains of HIV-1. We have confirmed the role of the A-opioid receptor based on the ability of a mu-opioid receptor-selective antagonist to block the effects of DAMGO. We have also found that morphine enhances CXCR4 and CCR5 expression and subsequently increases both X4 and R5 HIV-1 infection. We suggest that the capacity of tL-opioids to increase HIV-1 coreceptor expression and replication may promote viral binding, trafficking of HIV-1-infected cells, and enhanced disease progression. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:99 / 107
页数:9
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