Pereira Estela A, daSilva Luis L P
Department of Cell and Molecular Biology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
Traffic. 2016 Sep;17(9):976-96. doi: 10.1111/tra.12412. Epub 2016 Jun 3.
The Nef protein of the human immunodeficiency virus is a crucial determinant of viral pathogenesis and disease progression. Nef is abundantly expressed early in infection and is thought to optimize the cellular environment for viral replication. Nef controls expression levels of various cell surface molecules that play important roles in immunity and virus life cycle, by directly interfering with the itinerary of these proteins within the endocytic and late secretory pathways. To exert these functions, Nef physically interacts with host proteins that regulate protein trafficking. In recent years, considerable progress was made in identifying host-cell-interacting partners for Nef, and the molecular machinery used by Nef to interfere with protein trafficking has started to be unraveled. Here, we briefly review the knowledge gained and discuss new findings regarding the mechanisms by which Nef modifies the intracellular trafficking pathways to prevent antigen presentation, facilitate viral particle release and enhance the infectivity of HIV-1 virions.
人类免疫缺陷病毒的Nef蛋白是病毒发病机制和疾病进展的关键决定因素。Nef在感染早期大量表达,被认为可优化病毒复制的细胞环境。Nef通过直接干扰内吞和晚期分泌途径中这些蛋白质的行程,控制在免疫和病毒生命周期中起重要作用的各种细胞表面分子的表达水平。为发挥这些功能,Nef与调节蛋白质运输的宿主蛋白发生物理相互作用。近年来,在确定Nef的宿主细胞相互作用伙伴方面取得了相当大的进展,Nef用于干扰蛋白质运输的分子机制也已开始被揭示。在此,我们简要回顾所获得的知识,并讨论关于Nef修饰细胞内运输途径以防止抗原呈递、促进病毒颗粒释放并增强HIV-1病毒体感染性的机制的新发现。