Deng H K, Unutmaz D, KewalRamani V N, Littman D R
Division of Molecular Pathogenesis, Skirball Institute of Biomolecular Medicine, Howard Hughes Medical Institute, New York University Medical Center, New York 10016, USA.
Nature. 1997 Jul 17;388(6639):296-300. doi: 10.1038/40894.
Several members of the chemokine-receptor family serve, in conjunction with CD4, as receptors for the entry of human immunodeficiency virus type I (HIV-1) into cells. The principal receptor for entry of macrophage-tropic (M-tropic) HIV-1 strains is CCR5, whereas that for T-cell-line-tropic (T-tropic) strains is CXCR4. Unlike HIV-1, infection with either M-tropic or T-tropic strains of simian immunodeficiency virus (SIV) can be mediated by CCR5, but not CXCR4. SIV strains will also infect CD4+ cells that lack CCR5, which suggests that these strains use as yet unidentified receptors. Here we use an expression-cloning strategy to identify SIV receptors and have isolated genes encoding two members of the seven-transmembrane G-protein-coupled receptor family that are used not only by SIVs, but also by strains of HIV-2 and M-tropic HIV-1. Both receptors are closely related to the chemokine-receptor family and are expressed in lymphoid tissues. One of the receptors is also expressed in colon and may therefore be important in viral transmission. Usage of these new receptors following experimental infection of non-human primates with SIV strains may provide important insight into viral transmission and the mechanisms of SIV- and HIV-induced acquired immune-deficiency syndrome.
趋化因子受体家族的几个成员与CD4共同作为I型人类免疫缺陷病毒(HIV-1)进入细胞的受体。嗜巨噬细胞性(M-嗜性)HIV-1毒株进入细胞的主要受体是CCR5,而T细胞系嗜性(T-嗜性)毒株的主要受体是CXCR4。与HIV-1不同,猿猴免疫缺陷病毒(SIV)的M-嗜性或T-嗜性毒株感染均可由CCR5介导,但不能由CXCR4介导。SIV毒株也会感染缺乏CCR5的CD4+细胞,这表明这些毒株使用尚未确定的受体。在这里,我们使用表达克隆策略来鉴定SIV受体,并分离出编码七跨膜G蛋白偶联受体家族两个成员的基因,这些基因不仅被SIV使用,也被HIV-2毒株和M-嗜性HIV-1使用。这两种受体都与趋化因子受体家族密切相关,并在淋巴组织中表达。其中一种受体也在结肠中表达,因此可能在病毒传播中起重要作用。用SIV毒株对非人灵长类动物进行实验性感染后这些新受体的使用情况,可能会为病毒传播以及SIV和HIV诱导的获得性免疫缺陷综合征的机制提供重要见解。