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在COS细胞中,Vpu既能稳定束缚素的表达,又能抵消其抗病毒活性。

In COS cells Vpu can both stabilize tetherin expression and counteract its antiviral activity.

作者信息

Waheed Abdul A, Kuruppu Nishani D, Felton Kathryn L, D'Souza Darren, Freed Eric O

机构信息

Virus-Cell Interaction Section, HIV Drug Resistance Program, NCI-Frederick, Frederick, Maryland, United States of America.

出版信息

PLoS One. 2014 Oct 31;9(10):e111628. doi: 10.1371/journal.pone.0111628. eCollection 2014.

DOI:10.1371/journal.pone.0111628
PMID:25360760
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4216104/
Abstract

The interferon-inducible cellular protein tetherin (CD317/BST-2) inhibits the release of a broad range of enveloped viruses. The HIV-1 accessory protein Vpu enhances virus particle release by counteracting this host restriction factor. While the antagonism of human tetherin by Vpu has been associated with both proteasomal and lysosomal degradation, the link between Vpu-mediated tetherin degradation and the ability of Vpu to counteract the antiviral activity of tetherin remains poorly understood. Here, we show that human tetherin is expressed at low levels in African green monkey kidney (COS) cells. However, Vpu markedly increases tetherin expression in this cell line, apparently by sequestering it in an internal compartment that bears lysosomal markers. This stabilization of tetherin by Vpu requires the transmembrane sequence of human tetherin. Although Vpu stabilizes human tetherin in COS cells, it still counteracts the ability of tetherin to suppress virus release. The enhancement of virus release by Vpu in COS cells is associated with a modest reduction in cell-surface tetherin expression, even though the overall expression of tetherin is higher in the presence of Vpu. This study demonstrates that COS cells provide a model system in which Vpu-mediated enhancement of HIV-1 release is uncoupled from Vpu-mediated tetherin degradation.

摘要

干扰素诱导的细胞蛋白束缚素(CD317/BST-2)可抑制多种包膜病毒的释放。HIV-1辅助蛋白Vpu通过对抗这种宿主限制因子来增强病毒颗粒的释放。虽然Vpu对人束缚素的拮抗作用与蛋白酶体和溶酶体降解都有关,但Vpu介导的束缚素降解与Vpu对抗束缚素抗病毒活性能力之间的联系仍知之甚少。在此,我们表明人束缚素在非洲绿猴肾(COS)细胞中低水平表达。然而,Vpu明显增加了该细胞系中束缚素的表达,显然是通过将其隔离在带有溶酶体标记物的内部区室中实现的。Vpu对束缚素的这种稳定作用需要人束缚素的跨膜序列。尽管Vpu在COS细胞中稳定了人束缚素,但它仍然能够对抗束缚素抑制病毒释放的能力。Vpu在COS细胞中增强病毒释放与细胞表面束缚素表达的适度降低有关,即使在有Vpu存在的情况下束缚素的总体表达更高。这项研究表明,COS细胞提供了一个模型系统,其中Vpu介导的HIV-1释放增强与Vpu介导的束缚素降解脱钩。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/28cfef9ac47d/pone.0111628.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/0c558d8cacf7/pone.0111628.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/12e4ddf32730/pone.0111628.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/0cd8fc420ee5/pone.0111628.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/2116c5ab1729/pone.0111628.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/6d0b0f93dc5e/pone.0111628.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/30bf5dda5b4c/pone.0111628.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/28cfef9ac47d/pone.0111628.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/0c558d8cacf7/pone.0111628.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/12e4ddf32730/pone.0111628.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/0cd8fc420ee5/pone.0111628.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/2116c5ab1729/pone.0111628.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/6d0b0f93dc5e/pone.0111628.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/30bf5dda5b4c/pone.0111628.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/4216104/28cfef9ac47d/pone.0111628.g007.jpg

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Tetherin can restrict cell-free and cell-cell transmission of HIV from primary macrophages to T cells.束缚素可限制HIV从原代巨噬细胞到T细胞的无细胞和细胞间传播。
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Viruses. 2018 Oct 19;10(10):573. doi: 10.3390/v10100573.
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