Global profiling of viral and cellular non-coding RNAs in Epstein Barr virus-induced lymphoblastoid cell lines and released exosome cargos

被引:43
作者
Gallo, Alessia [1 ]
Vella, Serena [1 ]
Miele, Monica [2 ]
Timoneri, Francesca [2 ]
Di Bella, Mariangela [2 ]
Bosi, Silvia [2 ]
Sciveres, Marco [3 ]
Conaldi, Pier Giulio [1 ,2 ]
机构
[1] IRCCS ISMETT, Dept Lab Med & Adv Biotechnol, Rome, Italy
[2] Fondazione Ri MED, Palermo, Italy
[3] Univ Pittsburgh, Med Ctr, IRCCS ISMETI, Pediatr Hepatol & Liver Transplantat, Palermo, Italy
关键词
Epstein Barr virus; Lymphoblastoid cell lines; miRNA; IncRNA; Exosomes; EXTRACELLULAR VESICLES; B-CELLS; PHARMACOGENOMIC DISCOVERY; IN-VITRO; EXPRESSION; DNA; P53; GROWTH; MICROVESICLES; PATHOGENESIS;
D O I
10.1016/j.canlet.2016.12.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human EBV-transformed lymphoblastoid cell line (LCL), obtained by infecting peripheral blood monocular cells with Epstein Barr Virus, has been extensively used for human genetic, pharmacogenomic, and immunologic studies. Recently, the role of exosomes has also been indicated as crucial in the crosstalk between EBV and the host microenvironment. Because the role that the LCL and LCL exosomal cargo might play in maintaining persistent infection, and since little is known regarding the non-coding RNAs of LCL, the aim of our work was the comprehensive characterization of this class of RNA, cellular and viral miRNAs, and cellular lncRNAs, in LCL compared with PBMC derived from the same donors. In this study, we have demonstrated, for the first time, that all the viral miRNAs expressed by LCL are also packaged in the exosomes, and we found that two miRNAs, ebv-miR-BART3 and ebv-miR-BHRF1-1, are more abundant in the exosomes, suggesting a microvescicular viral microRNA transfer. In addition, IncRNA profiling revealed that LCLs were enriched in IncRNA H19 and H19 antisense, and released these through exosomes, suggesting a leading role in the regulation of the tumor microenvironment. (C) 2016 The Authors. Published by Elsevier Ireland Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:334 / 343
页数:10
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