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HIV Enters Cells via Endocytosis and Dynamin-Dependent Fusion with Endosomes

机译:HIV通过内吞作用和动力蛋白依赖的融合与内体进入细胞

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Enveloped viruses that rely on a low pH-dependent step for entry initiate infection by fusing with acidic endosomes, whereas the entry sites for pH-independent viruses, such as HIV-1, have not been defined. These viruses have long been assumed to fuse directly with the plasma membrane. Here we used population-based measurements of the viral content delivery into the cytosol and time-resolved imaging of single viruses to demonstrate that complete IV-1 fusion occurred in endosomes. In contrast, viral fusion with the plasma membrane did not progress beyond the lipid mixing step. HIV-1 underwent receptor-mediated internalization long before endosomal fusion, thus minimizing the surface exposure of conserved viral epitopes during fusion and reducing the efficacy of inhibitors targeting these epitopes. We also show that, strikingly, endosomal fusion is sensitive to a dynamin inhibitor, dynasore. These findings imply that HIV-1 infects cells via endocytosis and envelope glycoprotein- and dynamin-dependent fusion with intracellular compartments.
机译:依靠低pH依赖性步骤进入的被包膜病毒通过与酸性内体融合而开始感染,而尚未确定pH依赖性病毒(例如HIV-1)的进入位点。长期以来,一直认为这些病毒会直接与质膜融合。在这里,我们使用基于人群的病毒含量传递到细胞质中的测量以及单个病毒的时间分辨成像来证明内体中发生了完全的IV-1融合。相反,病毒与质膜的融合没有超出脂质混合步骤。 HIV-1在内体融合之前很久就经历了受体介导的内在化,因此使融合过程中保守的病毒表位的表面暴露最小化,并降低了针对这些表位的抑制剂的功效。我们还显示,引人注目的是,内体融合对动力抑制剂dynasore敏感。这些发现暗示HIV-1通过胞吞作用以及包膜糖蛋白和动力蛋白依赖性融合与细胞内区室感染细胞。

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