Raab-Traub Nancy, Dittmer Dirk P
UNC Lineberger Comprehensive Cancer Center, School of Medicine, University of North Carolina at Chapel Hill, CB# 7295, Chapel Hill, North Carolina 27599-7295, USA.
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, 125 Mason Farm Road, Chapel Hill, North Carolina 27599-7290, USA.
Nat Rev Microbiol. 2017 Sep;15(9):559-572. doi: 10.1038/nrmicro.2017.60. Epub 2017 Jun 26.
The release of membrane-bound vesicles from cells is being increasingly recognized as a mechanism of intercellular communication. Extracellular vesicles (EVs) or exosomes are produced by virus-infected cells and are thought to be involved in intercellular communication between infected and uninfected cells. Viruses, in particular oncogenic viruses and viruses that establish chronic infections, have been shown to modulate the production and content of EVs. Viral microRNAs, proteins and even entire virions can be incorporated into EVs, which can affect the immune recognition of viruses or modulate neighbouring cells. In this Review, we discuss the roles that EVs have during viral infection to either promote or restrict viral replication in target cells. We will also discuss our current understanding of the molecular mechanisms that underlie these roles, the potential consequences for the infected host and possible future diagnostic applications.
细胞释放膜结合囊泡作为一种细胞间通讯机制正日益受到认可。细胞外囊泡(EVs)或外泌体由病毒感染的细胞产生,被认为参与感染细胞与未感染细胞之间的细胞间通讯。病毒,特别是致癌病毒和建立慢性感染的病毒,已被证明可调节EVs的产生和内容物。病毒微小RNA、蛋白质甚至完整的病毒粒子都可被纳入EVs,这会影响病毒的免疫识别或调节邻近细胞。在本综述中,我们讨论了EVs在病毒感染期间对靶细胞中病毒复制的促进或限制作用。我们还将讨论目前对这些作用背后分子机制的理解、对受感染宿主的潜在影响以及未来可能的诊断应用。