Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/19559
Title: Muscle‐derived exosomes encapsulate myomiRs and are involved in local skeletal muscle tissue communication
Authors: Mytidou, Chrystalla 
Koutsoulidou, Andrie 
Katsioloudi, Anna 
Prokopi, Marianna 
Kapnisis, Konstantinos 
Michailidou, Kyriaki 
Anayiotos, Andreas 
Phylactou, Leonidas 
Major Field of Science: Medical and Health Sciences
Field Category: Mechanical Engineering
Keywords: Exosomal cross talk;Exosomes;MyomiRs;Skeletal muscle
Issue Date: 23-Jan-2021
Source: The FASEB Journal, 2021, vol. 35, no. 2, articl. no, e21279
Volume: 35
Issue: 2
Journal: The FASEB Journal 
Abstract: Exosomes are extracellular vesicles that are released from most cell types encap-sulating specific molecular cargo. Exosomes serve as mediators of cell-to-cell and tissue-to-tissue communications under normal and pathological conditions. It has been shown that exosomes carrying muscle-specific miRNAs, myomiRs, are se-creted from skeletal muscle cells in vitro and are elevated in the blood of muscle disease patients. The aim of this study was to investigate the secretion of exosomes encapsulating the four myomiRs from skeletal muscle tissues and to assess their role in inter-tissue communication between neighboring skeletal muscles in vivo. We demonstrate, for the first time, that isolated, intact skeletal muscle tissues secrete exosomes encapsulating the four myomiRs, miR-1, miR-133a, miR-133b, and miR-206. Notably, we show that the sorting of the four myomiRs within exosomes var-ies between skeletal muscles of different muscle fiber-type composition. miR-133a and miR-133b downregulation in TA muscles caused a reduction of their levels in neighboring skeletal muscles and in serum exosomes. In conclusion, our results re-veal that skeletal muscle-derived exosomes encapsulate the four myomiRs, some of which enter the blood, while a portion is used for the local communication between proximal muscle tissues. These findings provide important evidence regarding novel pathways implicated in skeletal muscle function.
URI: https://hdl.handle.net/20.500.14279/19559
ISSN: 15306860
DOI: 10.1096/fj.201902468RR
Rights: © The Authors
Type: Article
Affiliation : Cyprus Institute of Neurology and Genetics 
Theramir Ltd 
Cyprus University of Technology 
German Oncology Center 
Appears in Collections:Άρθρα/Articles

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