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Microtubule-dependent retrograde transport of bovine immunodeficiency virus

机译:牛免疫缺陷病毒的微管依赖性逆行转运

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摘要

Summary: Microtubules are essential components of the cytoskeleton that participate in a variety of cellular processes such as cell division and migration. In addition, there is a growing body of evidence implicating a role for microtubules in intracellular viral transport. In this study, we found that pharmacological disruption of microtubules remarkably blocked bovine immunodeficiency virus (BIV) movement from the cell periphery to the perinuclear region, a process known as retrograde transport. A similar effect was observed by inhibiting function of the microtubule-associated motor protein dynein. By yeast two-hybrid assay, we found that the capsid protein (CA) of BIV interacted with the dynein light-chain component LC8. Immunoprecipitation and GST-pulldown assays further demonstrated an interaction between CA and LC8 in mammalian cells. In addition, our data revealed LC8 as a linker between BIV particles and microtubules. Retrograde transport of BIV was significantly inhibited by knockdown of LC8 expression. Our findings present the first evidence that incoming BIV particles employ host microtubule/dynein machinery for transport towards the perinuclear region. In addition, our data indicate that the LC8-CA interaction is a potential target for the design of antiviral strategies.
机译:简介:微管是细胞骨架的重要组成部分,它参与各种细胞过程,例如细胞分裂和迁移。另外,越来越多的证据表明微管在细胞内病毒运输中的作用。在这项研究中,我们发现微管的药理学破坏显着阻断了牛免疫缺陷病毒(BIV)从细胞边缘向核周区域的移动,这一过程称为逆行运输。通过抑制微管相关运动蛋白达因的功能观察到了类似的效果。通过酵母双杂交测定,我们发现BIV的衣壳蛋白(CA)与动力蛋白轻链组分LC8相互作用。免疫沉淀和GST下拉试验进一步证明了哺乳动物细胞中CA和LC8之间的相互作用。此外,我们的数据显示LC8是BIV颗粒与微管之间的连接子。敲低LC8表达可显着抑制BIV的逆行转运。我们的发现提供了第一个证据,即传入的BIV颗粒利用宿主微管/动力蛋白机器向核周区域运输。此外,我们的数据表明,LC8-CA相互作用是抗病毒策略设计的潜在目标。

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