Preußer Christian, Hung Lee-Hsueh, Schneider Tim, Schreiner Silke, Hardt Martin, Moebus Anna, Santoso Sentot, Bindereif Albrecht
Institute of Biochemistry, Justus Liebig University of Giessen, Giessen, Germany.
Biomedical Research Centre Seltersberg, Imaging Unit, Justus Liebig University of Giessen, Giessen, Germany.
J Extracell Vesicles. 2018 Jan 15;7(1):1424473. doi: 10.1080/20013078.2018.1424473. eCollection 2018.
Circular RNAs (circRNAs) are a novel class of noncoding RNAs present in all eukaryotic cells investigated so far and generated by a special mode of alternative splicing of pre-mRNAs. Thereby, single exons, or multiple adjacent and spliced exons, are released in a circular form. CircRNAs are cell-type specifically expressed, are unusually stable, and can be found in various body fluids such as blood and saliva. Here we analysed circRNAs and the corresponding linear splice isoforms from human platelets, where circRNAs are particularly abundant, compared with other hematopoietic cell types. In addition, we isolated extracellular vesicles from purified and activated human platelets, using density-gradient centrifugation, followed by RNA-seq analysis for circRNA detection. We could demonstrate that circRNAs are packaged and released within both types of vesicles (microvesicles and exosomes) derived from platelets. Interestingly, we observed a selective release of circRNAs into the vesicles, suggesting a specific sorting mechanism. In sum, circRNAs represent yet another class of extracellular RNAs that circulate in the body and may be involved in signalling pathways. Since platelets are essential for central physiological processes such as haemostasis, wound healing, inflammation and cancer metastasis, these findings should greatly extend the potential of circRNAs as prognostic and diagnostic biomarkers.
环状RNA(circRNAs)是一类新型的非编码RNA,存在于目前所研究的所有真核细胞中,由前体信使核糖核酸(pre-mRNAs)的一种特殊可变剪接模式产生。由此,单个外显子或多个相邻且已剪接的外显子以环状形式释放。circRNAs具有细胞类型特异性表达,异常稳定,且可在血液和唾液等多种体液中发现。在此,我们分析了来自人血小板的circRNAs及其相应的线性剪接异构体,与其他造血细胞类型相比,血小板中的circRNAs尤为丰富。此外,我们使用密度梯度离心法从纯化并激活的人血小板中分离细胞外囊泡,随后进行RNA测序分析以检测circRNAs。我们能够证明circRNAs被包装并释放于源自血小板的两种类型的囊泡(微囊泡和外泌体)中。有趣的是,我们观察到circRNAs选择性地释放到囊泡中,提示存在一种特定的分选机制。总之,circRNAs代表了另一类在体内循环且可能参与信号通路的细胞外RNA。由于血小板对于止血、伤口愈合、炎症和癌症转移等核心生理过程至关重要,这些发现应极大地扩展circRNAs作为预后和诊断生物标志物的潜力。