WIN55,212-2-mediated inhibition of HIV-1 expression in microglial cells: Involvement of cannabinoid receptors

被引:47
作者
Rock, R. Bryan
Gekker, Genya
Hu, Shuxian
Sheng, Wen S.
Cabral, Guy A.
Martin, Billy R.
Peterson, Phillip K.
机构
[1] Univ Minnesota, Dept Med, Div Infect Dis & Int Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Ctr Infect Dis & Microbiol Translat Res, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[4] Virginia Commonwealth Univ, Dept Microbiol & Immunol, Richmond, VA 23298 USA
[5] Virginia Commonwealth Univ, Dept Pharmacol & Toxicol, Richmond, VA 23298 USA
关键词
cannabinoids; HIV-1; microglia; WIN55,212-2; SR141716A;
D O I
10.1007/s11481-006-9040-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cannabinoid receptors CB1 and CB2 are primarily expressed in cells of the nervous and immune systems, respectively. Recently, the synthetic CB1/CB2 agonist WIN55,212-2 was found to suppress replication of HIV-1 in microglial cell cultures. The present study was undertaken to test the hypothesis that WIN 55,212-2's antiviral effect is mediated via CB2 receptors. By reverse transcription-polymerase chain reaction, microglia were found to express both CB, and CB2 receptors. Using additional CBI/ CB2 receptor agonists and selective antagonists, we found that CB2 receptors are involved in WIN55,212-2's antiviral activity and surprisingly that the CB, receptor-selective antagonist SR141716A behaved as an agonist in these brain macrophages.
引用
收藏
页码:178 / 183
页数:6
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