Bounou Salim, Giguere Jean-François, Cantin Réjean, Gilbert Caroline, Imbeault Michael, Martin Geneviève, Tremblay Michel J
Research Center in Infectious Diseases, CHUL Research Center, and Faculty of Medicine, Laval University, Quebec, Canada.
FASEB J. 2004 Aug;18(11):1294-6. doi: 10.1096/fj.04-1755fje. Epub 2004 Jun 18.
The primary objective of this study was to define whether the nature of virion-bound host cell membrane proteins influenced the process of human immunodeficiency virus 1 (HIV-1) capture and transmission. We pulsed cells of monocytoid lineage (established and primary) and CD4-negative epithelial cells transiently expressing DC-SIGN or LFA-1 with isogenic HIV-1 particles either devoid or bearing host-derived ICAM-1 or ICAM-3 before incubation with an indicator cell line. To our surprise, the ICAM-1/LFA-1 association was a more efficient transmission factor than the combined gp120/DC-SIGN and ICAM-3/DC-SIGN interactions. The involvement of the association between virus-bound ICAM-1 and its natural ligand LFA-1 in virus binding and carriage was confirmed when using more physiological cellular targets, i.e., human lymphoid tissues cultured ex vivo. However, the contribution of virus-anchored host ICAM-1 to the process of retention and transmission of HIV-1 could not be confirmed when using primary human cells of macrophage/dendritic lineage as transmitter cells and autologous CD4+ T lymphocytes as targets. Altogether these data underscore the complexity of factors participating in virus-cell contact and efficient dissemination of HIV-1 to target cells.
本研究的主要目的是确定病毒体结合的宿主细胞膜蛋白的性质是否会影响人类免疫缺陷病毒1型(HIV-1)的捕获和传播过程。在与指示细胞系孵育之前,我们用不含或携带宿主来源的细胞间黏附分子-1(ICAM-1)或ICAM-3的同基因HIV-1颗粒脉冲处理单核细胞系(已建立的和原代的)细胞以及瞬时表达DC-SIGN或淋巴细胞功能相关抗原-1(LFA-1)的CD4阴性上皮细胞。令我们惊讶的是,ICAM-1/LFA-1结合比gp120/DC-SIGN和ICAM-3/DC-SIGN相互作用的组合更有效地促进病毒传播。当使用更接近生理状态的细胞靶点,即体外培养的人类淋巴组织时,病毒结合的ICAM-1与其天然配体LFA-1之间的结合在病毒结合和携带中的作用得到了证实。然而,当使用巨噬细胞/树突状细胞系的原代人类细胞作为传递细胞,自体CD4+T淋巴细胞作为靶点时,病毒锚定的宿主ICAM-1对HIV-1的滞留和传播过程的贡献无法得到证实。总之,这些数据强调了参与病毒-细胞接触以及HIV-1向靶细胞高效传播的因素的复杂性。