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柯萨奇病毒 B3 诱导的细胞突起:结构特征和功能能力。

Coxsackievirus B3-induced cellular protrusions: structural characteristics and functional competence.

机构信息

Nanoscience Center, Department of Biological and Environmental Science, University of Jyväskylä, Finland.

出版信息

J Virol. 2011 Jul;85(13):6714-24. doi: 10.1128/JVI.00247-10. Epub 2011 Apr 27.

DOI:10.1128/JVI.00247-10
PMID:21525342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3126532/
Abstract

Virus-induced alterations in cell morphology play important roles in the viral life cycle. To examine the intracellular events of coxsackievirus B3 (CVB3) infection, green monkey kidney (GMK) cells were either inoculated with the virus or transfected with the viral RNA. Various microscopic and flow cytometric approaches demonstrated the emergence of CVB3 capsid proteins at 8 h posttransfection, followed by morphological transformation of the cells. The morphological changes included formation of membranous protrusions containing viral capsids, together with microtubules and actin. Translocation of viral capsids into these protrusions was sensitive to cytochalasin D, suggesting the importance of actin in the process. Three-dimensional (3D) live-cell imaging demonstrated frequent contacts between cellular protrusions and adjacent cells. Markedly, in spite of an increase in the cellular viral protein content starting 8 h postinfection, no significant decrease in cell viability or increase in the amount of early apoptotic markers was observed by flow cytometry by 28 h postinfection. Comicroinjection of viral RNA and fluorescent dextran in the presence of neutralizing virus antibody suggested that these protrusions mediated the spread of infection from one cell to another prior to virus-induced cell lysis. Altogether, the CVB3-induced cellular protrusions could function as a hitherto-unknown nonlytic mechanism of cell-to-cell transmission exploited by enteroviruses.

摘要

病毒诱导的细胞形态改变在病毒生命周期中起着重要作用。为了研究柯萨奇病毒 B3(CVB3)感染的细胞内事件,用病毒感染绿猴肾(GMK)细胞或用病毒 RNA 转染细胞。各种显微镜和流式细胞术方法表明,CVB3 衣壳蛋白在转染后 8 小时出现,随后细胞发生形态转化。这些形态变化包括形成含有病毒衣壳的膜状突起,同时还有微管和肌动蛋白。病毒衣壳向这些突起的易位对细胞松弛素 D 敏感,表明肌动蛋白在该过程中的重要性。三维(3D)活细胞成像显示细胞突起与相邻细胞之间频繁接触。值得注意的是,尽管在感染后 8 小时开始细胞内病毒蛋白含量增加,但在感染后 28 小时通过流式细胞术观察到细胞活力没有明显下降,早期凋亡标志物的含量也没有增加。在中和病毒抗体存在的情况下共微注射病毒 RNA 和荧光葡聚糖表明,这些突起介导了感染从一个细胞传播到另一个细胞,而在病毒诱导的细胞裂解之前。总之,CVB3 诱导的细胞突起可作为迄今未知的肠病毒利用的非溶细胞性细胞间传播的机制。

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