Petrik Juraj
Scottish National Blood Transfusion Service and University of Edinburgh, Edinburgh, UK.
Transfus Apher Sci. 2016 Aug;55(1):84-91. doi: 10.1016/j.transci.2016.07.014. Epub 2016 Jul 15.
Viruses have developed a spectrum of ways to modify cellular pathways to hijack the cell machinery for the synthesis of their nucleic acid and proteins. Similarly, they use intracellular vesicular mechanisms of trafficking for their assembly and eventual release, with a number of viruses acquiring their envelope from internal or plasma cell membranes. There is an increasing number of reports on viral exploitation of cell secretome pathways to avoid recognition and stimulation of the immune response. Extracellular vesicles (EV) containing viral particles have been shown to shield viruses after exiting the host cell, in some cases challenging the boundaries between viral groups traditionally characterised as enveloped and non-enveloped. Apart from viral particles, EV can spread the virus also carrying viral genome and can modify the target cells through their cargo of virus-coded miRNAs and proteins as well as selectively packaged cellular mRNAs, miRNAs, proteins and lipids, differing in composition and quantities from the cell of origin.
病毒已发展出一系列方法来改变细胞途径,以劫持细胞机制来合成其核酸和蛋白质。同样,它们利用细胞内囊泡运输机制进行组装并最终释放,许多病毒从内质网或质膜获取其包膜。关于病毒利用细胞分泌组途径来逃避免疫反应的识别和刺激的报道越来越多。含有病毒颗粒的细胞外囊泡(EV)已被证明在离开宿主细胞后能保护病毒,在某些情况下模糊了传统上被归类为包膜病毒和非包膜病毒的界限。除了病毒颗粒外,EV还可以传播携带病毒基因组的病毒,并可通过其携带的病毒编码的微小RNA(miRNA)和蛋白质以及选择性包装的细胞mRNA、miRNA、蛋白质和脂质来修饰靶细胞,其组成和数量与来源细胞不同。