Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/19559
DC FieldValueLanguage
dc.contributor.authorMytidou, Chrystalla-
dc.contributor.authorKoutsoulidou, Andrie-
dc.contributor.authorKatsioloudi, Anna-
dc.contributor.authorProkopi, Marianna-
dc.contributor.authorKapnisis, Konstantinos-
dc.contributor.authorMichailidou, Kyriaki-
dc.contributor.authorAnayiotos, Andreas-
dc.contributor.authorPhylactou, Leonidas-
dc.date.accessioned2021-02-09T10:03:50Z-
dc.date.available2021-02-09T10:03:50Z-
dc.date.issued2021-01-23-
dc.identifier.citationThe FASEB Journal, 2021, vol. 35, no. 2, articl. no, e21279en_US
dc.identifier.issn15306860-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/19559-
dc.description.abstractExosomes 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.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofThe FASEB Journalen_US
dc.rights© The Authorsen_US
dc.subjectExosomal cross talken_US
dc.subjectExosomesen_US
dc.subjectMyomiRsen_US
dc.subjectSkeletal muscleen_US
dc.titleMuscle‐derived exosomes encapsulate myomiRs and are involved in local skeletal muscle tissue communicationen_US
dc.typeArticleen_US
dc.collaborationCyprus Institute of Neurology and Geneticsen_US
dc.collaborationTheramir Ltden_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationGerman Oncology Centeren_US
dc.subject.categoryMechanical Engineeringen_US
dc.journalsOpen Accessen_US
dc.countryCyprusen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1096/fj.201902468RRen_US
dc.relation.issue2en_US
dc.relation.volume35en_US
cut.common.academicyear2020-2021en_US
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.author.deptDepartment of Mechanical Engineering and Materials Science and Engineering-
crisitem.author.deptDepartment of Mechanical Engineering and Materials Science and Engineering-
crisitem.author.deptDepartment of Mechanical Engineering and Materials Science and Engineering-
crisitem.author.facultyFaculty of Engineering and Technology-
crisitem.author.facultyFaculty of Engineering and Technology-
crisitem.author.facultyFaculty of Engineering and Technology-
crisitem.author.orcid0000-0003-4123-3065-
crisitem.author.orcid0000-0002-4999-0231-
crisitem.author.orcid0000-0003-4471-7604-
crisitem.author.parentorgFaculty of Engineering and Technology-
crisitem.author.parentorgFaculty of Engineering and Technology-
crisitem.author.parentorgFaculty of Engineering and Technology-
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