Section of Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, MA, USA.
The Buck Institute for Research on Aging, Novato, CA, USA.
Nature. 2022 Jan;601(7893):446-451. doi: 10.1038/s41586-021-04234-3. Epub 2021 Dec 22.
Exosomes and other small extracellular vesicles (sEVs) provide a unique mode of cell-to-cell communication in which microRNAs (miRNAs) produced and released from one cell are taken up by cells at a distance where they can enact changes in gene expression. However, the mechanism by which miRNAs are sorted into exosomes/sEVs or retained in cells remains largely unknown. Here we demonstrate that miRNAs possess sorting sequences that determine their secretion in sEVs (EXOmotifs) or cellular retention (CELLmotifs) and that different cell types, including white and brown adipocytes, endothelium, liver and muscle, make preferential use of specific sorting sequences, thus defining the sEV miRNA profile of that cell type. Insertion or deletion of these CELLmotifs or EXOmotifs in a miRNA increases or decreases retention in the cell of production or secretion into exosomes/sEVs. Two RNA-binding proteins, Alyref and Fus, are involved in the export of miRNAs carrying one of the strongest EXOmotifs, CGGGAG. Increased miRNA delivery mediated by EXOmotifs leads to enhanced inhibition of target genes in distant cells. Thus, this miRNA code not only provides important insights that link circulating exosomal miRNAs to tissues of origin, but also provides an approach for improved targeting in RNA-mediated therapies.
外泌体和其他小细胞外囊泡 (sEVs) 提供了一种独特的细胞间通讯方式,其中一个细胞产生和释放的 microRNAs (miRNAs) 被远处的细胞摄取,从而在远处的细胞中引发基因表达的变化。然而,miRNAs 如何被分拣到外泌体/sEVs 中或保留在细胞中的机制在很大程度上仍然未知。在这里,我们证明了 miRNAs 具有决定其在 sEVs 中分泌 (EXOmotifs) 或在细胞中保留 (CELLmotifs) 的分拣序列,并且不同的细胞类型,包括白色和棕色脂肪细胞、内皮细胞、肝脏和肌肉,优先使用特定的分拣序列,从而定义了该细胞类型的 sEV miRNA 特征。在 miRNA 中插入或删除这些 CELLmotifs 或 EXOmotifs 会增加或减少其在产生细胞中的保留或分泌到外泌体/sEVs 中的数量。两种 RNA 结合蛋白 Alyref 和 Fus 参与了携带最强 EXOmotif(CCCCGGA)之一的 miRNAs 的输出。EXOmotifs 介导的 miRNA 传递增加会导致靶基因在远处细胞中的抑制增强。因此,这个 miRNA 密码不仅提供了将循环外泌体 miRNAs 与起源组织联系起来的重要见解,而且还为 RNA 介导的治疗中提高靶向性提供了一种方法。