Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia 20147.
The Virus-Cell Interaction Section, HIV Dynamics and Replication Program, National Cancer Institute, Frederick, Maryland 21701.
Annu Rev Virol. 2017 Sep 29;4(1):309-325. doi: 10.1146/annurev-virology-101416-041840. Epub 2017 Jul 17.
The strong dependence of retroviruses, such as human immunodeficiency virus type 1 (HIV-1), on host cell factors is no more apparent than when the endosomal sorting complex required for transport (ESCRT) machinery is purposely disengaged. The resulting potent inhibition of retrovirus release underscores the importance of understanding fundamental structure-function relationships at the ESCRT-HIV-1 interface. Recent studies utilizing advanced imaging technologies have helped clarify these relationships, overcoming hurdles to provide a range of potential models for ESCRT-mediated virus abscission. Here, we discuss these models in the context of prior work detailing ESCRT machinery and the HIV-1 release process. To provide a template for further refinement, we propose a new working model for ESCRT-mediated HIV-1 release that reconciles disparate and seemingly conflicting studies.
逆转录病毒(如人类免疫缺陷病毒 1 型(HIV-1))强烈依赖宿主细胞因子,这在细胞内体分选复合物必需运输(ESCRT)机制被故意分离时表现得尤为明显。这种对逆转录病毒释放的有效抑制强调了理解 ESCRT-HIV-1 界面基本结构-功能关系的重要性。最近利用先进成像技术的研究有助于阐明这些关系,克服了一系列障碍,为 ESCRT 介导的病毒脱落提供了多种潜在模型。在这里,我们将这些模型放在详细描述 ESCRT 机制和 HIV-1 释放过程的先前工作的背景下进行讨论。为了提供进一步细化的模板,我们提出了一个新的 ESCRT 介导的 HIV-1 释放工作模型,该模型调和了看似相互矛盾的不同研究。