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腺病毒转导:比受体表达更复杂。

Adenovirus transduction: More complicated than receptor expression.

作者信息

Sharma Priyanka, Martis Prithy C, Excoffon Katherine J D A

机构信息

Department of Biological Sciences, Wright State University, Dayton, OH, USA.

Biomedical Sciences PhD Program, Wright State University, Dayton, OH 45435, USA.

出版信息

Virology. 2017 Feb;502:144-151. doi: 10.1016/j.virol.2016.12.020. Epub 2016 Dec 31.

Abstract

The abundance and accessibility of a primary virus receptor are critical factors that impact the susceptibility of a host cell to virus infection. The Coxsackievirus and adenovirus receptor (CAR) has two transmembrane isoforms that occur due to alternative splicing and differ in localization and function in polarized epithelia. To determine the relevance of isoform-specific expression across cell types, the abundance and localization of both isoforms were determined in ten common cell lines, and correlated with susceptibility to adenovirus transduction relative to polarized primary human airway epithelia. Data show that the gene and protein expression for each isoform of CAR varies significantly between cell lines and polarization, as indicated by high transepithelial resistance, is inversely related to adenovirus transduction. In summary, the variability of polarity and isoform-specific expression among model cells are critical parameters that must be considered when evaluating the clinical relevance of potential adenovirus-mediated gene therapy and anti-adenovirus strategies.

摘要

一种主要病毒受体的丰度和可及性是影响宿主细胞对病毒感染易感性的关键因素。柯萨奇病毒和腺病毒受体(CAR)有两种跨膜异构体,它们是由可变剪接产生的,在极化上皮细胞中的定位和功能有所不同。为了确定不同细胞类型中异构体特异性表达的相关性,在十种常见细胞系中测定了两种异构体的丰度和定位,并将其与相对于极化原代人气道上皮细胞的腺病毒转导易感性相关联。数据表明,CAR每种异构体的基因和蛋白质表达在不同细胞系和极化状态之间存在显著差异,高跨上皮电阻表明这种差异与腺病毒转导呈负相关。总之,模型细胞之间极性和异构体特异性表达的变异性是在评估潜在腺病毒介导的基因治疗和抗腺病毒策略的临床相关性时必须考虑的关键参数。

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本文引用的文献

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Adenovirus entry from the apical surface of polarized epithelia is facilitated by the host innate immune response.
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The PDZ1 and PDZ3 domains of MAGI-1 regulate the eight-exon isoform of the coxsackievirus and adenovirus receptor.
J Virol. 2012 Sep;86(17):9244-54. doi: 10.1128/JVI.01138-12. Epub 2012 Jun 20.
10

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