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MicroRNA sequence codes for small extracellular vesicle release and cellular retention

Author

Listed:
  • Ruben Garcia-Martin

    (Harvard Medical School)

  • Guoxiao Wang

    (Harvard Medical School)

  • Bruna B. Brandão

    (Harvard Medical School)

  • Tamires M. Zanotto

    (Harvard Medical School)

  • Samah Shah

    (The Buck Institute for Research on Aging)

  • Sandip Kumar Patel

    (The Buck Institute for Research on Aging)

  • Birgit Schilling

    (The Buck Institute for Research on Aging)

  • C. Ronald Kahn

    (Harvard Medical School)

Abstract

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 expression1–3. 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.

Suggested Citation

  • Ruben Garcia-Martin & Guoxiao Wang & Bruna B. Brandão & Tamires M. Zanotto & Samah Shah & Sandip Kumar Patel & Birgit Schilling & C. Ronald Kahn, 2022. "MicroRNA sequence codes for small extracellular vesicle release and cellular retention," Nature, Nature, vol. 601(7893), pages 446-451, January.
  • Handle: RePEc:nat:nature:v:601:y:2022:i:7893:d:10.1038_s41586-021-04234-3
    DOI: 10.1038/s41586-021-04234-3
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    Cited by:

    1. Jinhong Xu & Le Cui & Jiaqi Wang & Shasha Zheng & Huahua Zhang & Shuo Ke & Xiaoqin Cao & Yanteng Shi & Jing Li & Ke Zen & Antonio Vidal-Puig & Chen-Yu Zhang & Liang Li & Xiaohong Jiang, 2023. "Cold-activated brown fat-derived extracellular vesicle-miR-378a-3p stimulates hepatic gluconeogenesis in male mice," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    2. Weitao Zhang & Junfeng Lu & Lianshun Feng & Hanyue Xue & Shiyang Shen & Shuiqing Lai & PingPing Li & Ping Li & Jian Kuang & Zhiwei Yang & Xiaojun Xu, 2024. "Sonic hedgehog-heat shock protein 90β axis promotes the development of nonalcoholic steatohepatitis in mice," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    3. Xinyan Zhou & Mengchao Yu & Luzhen Ma & Jinyu Fu & Jingwei Guo & Jieqiong Lei & Zheng Fu & Yong Fu & Qipeng Zhang & Chen-Yu Zhang & Xi Chen, 2022. "In vivo self-assembled siRNA as a modality for combination therapy of ulcerative colitis," Nature Communications, Nature, vol. 13(1), pages 1-23, December.

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