Harmon Brooke, Ratner Lee
Division of Molecular Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
J Virol. 2008 Sep;82(18):9191-205. doi: 10.1128/JVI.00424-08. Epub 2008 Jul 16.
Binding of human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein (Env) with the primary receptor CD4 and one of two coreceptors, CXCR4 or CCR5, activates a signaling cascade resulting in Rac-1 GTPase activation and stimulation of actin cytoskeletal reorganizations critical for HIV-1-mediated membrane fusion. The mechanism by which HIV-1 Env induces Rac-1 activation and subsequent actin cytoskeleton rearrangement is unknown. In this study, we show that Env-mediated Rac-1 activation is dependent on the activation of Galpha(q) and its downstream targets. Fusion and Rac-1 activation are mediated by Galpha(q) and phospholipase C (PLC), as shown by attenuation of fusion and Rac-1 activation in cells either expressing small interfering RNA (siRNA) targeting Galpha(q) or treated with the PLC inhibitor U73122. Rac-1 activation and fusion were also blocked by multiple protein kinase C inhibitors, by inhibitors of intracellular Ca2+ release, by Pyk2-targeted siRNA, and by the Ras inhibitor S-trans,trans-farnesylthiosalicylic acid (FTS). Fusion was blocked without altering cell viability or cell surface localization of CD4 and CCR5. Similar results were obtained when cell fusion was induced by Env expressed on viral and cellular membranes and when cell lines or primary cells were the target. Treatment with inhibitors and siRNA specific for Galpha(i) or Galpha(s) signaling mediators had no effect on Env-mediated Rac-1 activation or cell fusion, indicating that the Galpha(q) pathway alone is responsible. These results could provide a new focus for therapeutic intervention with drugs targeting host signaling mediators rather than viral molecules, a strategy which is less likely to result in resistance.
人类免疫缺陷病毒1型(HIV-1)包膜糖蛋白(Env)与主要受体CD4以及两个共受体之一CXCR4或CCR5结合,会激活一个信号级联反应,导致Rac-1 GTP酶激活,并刺激对HIV-1介导的膜融合至关重要的肌动蛋白细胞骨架重排。HIV-1 Env诱导Rac-1激活及随后肌动蛋白细胞骨架重排的机制尚不清楚。在本研究中,我们表明Env介导的Rac-1激活依赖于Gαq及其下游靶点的激活。融合和Rac-1激活由Gαq和磷脂酶C(PLC)介导,这在表达靶向Gαq的小干扰RNA(siRNA)的细胞或用PLC抑制剂U73122处理的细胞中融合和Rac-1激活减弱的情况中得到体现。Rac-1激活和融合也被多种蛋白激酶C抑制剂、细胞内Ca2+释放抑制剂、靶向Pyk2的siRNA以及Ras抑制剂S-反式,反式-法尼基硫代水杨酸(FTS)所阻断。融合被阻断,但未改变细胞活力或CD4和CCR5的细胞表面定位。当由病毒和细胞膜上表达的Env诱导细胞融合时,以及当细胞系或原代细胞作为靶点时,均获得了类似结果。用对Gαi或Gαs信号介质特异的抑制剂和siRNA处理对Env介导的Rac-1激活或细胞融合没有影响,表明仅Gαq途径起作用。这些结果可能为以宿主信号介质而非病毒分子为靶点的药物治疗干预提供新的焦点,这种策略不太可能导致耐药性。