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细胞间传播可以克服细胞外 HIV 对供体细胞和靶细胞施加的多种障碍。

Cell-to-cell transmission can overcome multiple donor and target cell barriers imposed on cell-free HIV.

机构信息

Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT, USA.

出版信息

PLoS One. 2013;8(1):e53138. doi: 10.1371/journal.pone.0053138. Epub 2013 Jan 7.

Abstract

Virus transmission can occur either by a cell-free mode through the extracellular space or by cell-to-cell transmission involving direct cell-to-cell contact. The factors that determine whether a virus spreads by either pathway are poorly understood. Here, we assessed the relative contribution of cell-free and cell-to-cell transmission to the spreading of the human immunodeficiency virus (HIV). We demonstrate that HIV can spread by a cell-free pathway if all the steps of the viral replication cycle are efficiently supported in highly permissive cells. However, when the cell-free path was systematically hindered at various steps, HIV transmission became contact-dependent. Cell-to-cell transmission overcame barriers introduced in the donor cell at the level of gene expression and surface retention by the restriction factor tetherin. Moreover, neutralizing antibodies that efficiently inhibit cell-free HIV were less effective against cell-to-cell transmitted virus. HIV cell-to-cell transmission also efficiently infected target T cells that were relatively poorly susceptible to cell-free HIV. Importantly, we demonstrate that the donor and target cell types influence critically the extent by which cell-to-cell transmission can overcome each barrier. Mechanistically, cell-to-cell transmission promoted HIV spread to more cells and infected target cells with a higher proviral content than observed for cell-free virus. Our data demonstrate that the frequently observed contact-dependent spread of HIV is the result of specific features in donor and target cell types, thus offering an explanation for conflicting reports on the extent of cell-to-cell transmission of HIV.

摘要

病毒传播可以通过细胞外空间的无细胞模式或涉及直接细胞间接触的细胞间传播来发生。决定病毒通过哪种途径传播的因素了解甚少。在这里,我们评估了人类免疫缺陷病毒 (HIV) 以无细胞和细胞间途径传播的相对贡献。我们证明,如果在高度允许的细胞中有效地支持病毒复制周期的所有步骤,HIV 可以通过无细胞途径传播。然而,当无细胞途径在各个步骤被系统地阻碍时,HIV 传播就变得依赖于接触。细胞间传播克服了通过限制因子 tetherin 在供体细胞中在基因表达和表面保留水平上引入的障碍。此外,有效地抑制无细胞 HIV 的中和抗体对细胞间传播的病毒的效果较差。HIV 细胞间传播也有效地感染了对无细胞 HIV 相对不易感染的靶 T 细胞。重要的是,我们证明供体细胞和靶细胞类型严重影响细胞间传播克服每种障碍的程度。从机制上讲,细胞间传播促进了 HIV 向更多细胞的传播,并感染了靶细胞,其前病毒含量高于观察到的无细胞病毒。我们的数据表明,HIV 经常观察到的接触依赖性传播是供体和靶细胞类型的特定特征的结果,从而为 HIV 细胞间传播程度的相互矛盾的报告提供了解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468b/3538641/5f94d90ce788/pone.0053138.g001.jpg

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