Hoshina Shiho, Sekizuka Tsuyoshi, Kataoka Michiyo, Hasegawa Hideki, Hamada Hiromichi, Kuroda Makoto, Katano Harutaka
Department of Pathology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Department of Pediatrics, Yachiyo Medical Center, Tokyo Women's Medical University, 477-96 Owada-Shinden, Yachiyo, Chiba 276-0046, Japan.
PLoS One. 2016 Sep 9;11(9):e0162574. doi: 10.1371/journal.pone.0162574. eCollection 2016.
Exosomes are small vesicles released from cells, into which microRNAs (miRNA) are specifically sorted and accumulated. Two gamma-herpesviruses, Kaposi sarcoma-associated herpesvirus (KSHV) and Epstein-Barr virus (EBV), encode miRNAs in their genomes and express virus-encoded miRNAs in cells and exosomes. However, there is little information about the detailed distribution of virus-encoded miRNAs in cells and exosomes. In this study, we thus identified virus- and host-encoded miRNAs in exosomes released from KSHV- or EBV-infected lymphoma cell lines and compared them with intracellular miRNAs using a next-generation sequencer. Sequencing analysis demonstrated that 48% of the annotated miRNAs in the exosomes from KSHV-infected cells originated from KSHV. Human mir-10b-5p and mir-143-3p were much more highly concentrated in exosomes than in cells. Exosomes contained more nonexact mature miRNAs that did not exactly match those in miRBase than cells. Among the KSHV-encoded miRNAs, miRK12-3-5p was the most abundant exact mature miRNA in both cells and exosomes that exactly matched those in miRBase. Recently identified EXOmotifs, nucleotide motifs that control the loading of miRNAs into exosomes were frequently found within the sequences of KSHV-encoded miRNAs, and the presence of the EXOmotif CCCT or CCCG was associated with the localization of miRNA in exosomes in KSHV-infected cells. These observations suggest that specific virus-encoded miRNAs are sorted by EXOmotifs and accumulate in exosomes in virus-infected cells.
外泌体是细胞释放的小囊泡,微小RNA(miRNA)会特异性地分选并积累到其中。两种γ-疱疹病毒,即卡波西肉瘤相关疱疹病毒(KSHV)和爱泼斯坦-巴尔病毒(EBV),在其基因组中编码miRNA,并在细胞和外泌体中表达病毒编码的miRNA。然而,关于病毒编码的miRNA在细胞和外泌体中的详细分布情况,目前所知甚少。因此,在本研究中,我们鉴定了从KSHV或EBV感染的淋巴瘤细胞系释放的外泌体中病毒和宿主编码的miRNA,并使用新一代测序仪将它们与细胞内的miRNA进行比较。测序分析表明,来自KSHV感染细胞的外泌体中48%的注释miRNA源自KSHV。人类mir-10b-5p和mir-143-3p在外泌体中的浓度比在细胞中高得多。外泌体中包含的非精确成熟miRNA比细胞中更多,这些非精确成熟miRNA与miRBase中的序列不完全匹配。在KSHV编码的miRNA中,miRK12-3-5p是细胞和外泌体中最丰富的精确成熟miRNA,与miRBase中的序列完全匹配。最近发现的EXOmotifs,即控制miRNA加载到外泌体中的核苷酸基序,在KSHV编码的miRNA序列中经常被发现,并且EXOmotif CCCT或CCCG的存在与KSHV感染细胞中外泌体中miRNA的定位有关。这些观察结果表明,特定的病毒编码miRNA通过EXOmotifs进行分选,并在病毒感染的细胞中外泌体中积累。