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Cell-surface expression of CD4 reduces HIV-1 infectivity by blocking Env incorporation in a Nef- and Vpu-inhibitable manner

机译:CD4的细胞表面表达通过以Nef和Vpu抑制方式阻止Env掺入来降低HIV-1感染性

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Human immunodeficiency virus-1 (HIV-1) infection decreases the cell-surface expression of its cellular receptor, CD4, through the combined actions of Nef, Env and Vpu. Such functional convergence strongly suggests that CD4 downregulation is critical for optimal viral replication, yet the significance of this phenomenon has so far remained a puzzle. We show that high levels of CD4 on the surface of HIV-infected cells induce a dramatic reduction in the infectivity of released virions by the sequestering of the viral envelope by CD4. CD4 is able to accumulate in viral particles while at the same time blocking incorporation of Env into the virion. Nef and Vpu, through their ability to downregulate CD4, counteract this effect. The CD4-mediated `envelope interference' described here probably explains the plurality of mechanisms developed by HIV to downregulate the cell-surface expression of its receptor.
机译:人类免疫缺陷病毒1(HIV-1)感染通过Nef,Env和Vpu的联合作用降低其细胞受体CD4的细胞表面表达。这种功能的融合强烈表明CD4的下调对于最佳病毒复制至关重要,但是迄今为止,这种现象的重要性仍然令人困惑。我们显示高水平的CD4在HIV感染的细胞表面上通过CD4隔离病毒包膜诱导释放的病毒体的感染力急剧降低。 CD4能够积聚在病毒颗粒中,同时阻止Env掺入病毒粒子。 Nef和Vpu通过下调CD4的能力来抵消这种作用。这里描述的CD4介导的“包膜干扰”可能解释了HIV开发的多种机制,下调了其受体的细胞表面表达。

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