{"title":"Non-Invasive Ultrasound Treatment Enhances the Release of Skeletal Muscle-Derived Extracellular Vesicles in Mice","authors":"Atomu Yamaguchi, Xiaoqi Ma, Mikiko Uemura, Kento Tanida, Nozomi Nishimura, Jiaqi Tan, Gojiro Nakagami, Hiromi Sanada, Dongming Su, Kristopher Sarosiek, Hidemi Fujino, Noriaki Maeshige","doi":"10.1096/fj.202501797R","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Skeletal muscle, the largest secretory organ, regulates distant organs through the secretion of various factors. Among these are extracellular vesicles (EVs), which play a significant role in mediating communication between muscle and other tissues and hold therapeutic potential due to their target specificity and anti-inflammatory properties. Enhancing the release of EVs from skeletal muscle into the circulation is crucial for eliciting their diverse effects, including anti-inflammatory actions; however, effective strategies to increase the levels of muscle-derived EVs in the bloodstream have not yet been developed. While exercise is the most studied method to increase blood EV levels, its efficacy in enhancing skeletal muscle-derived EVs remains unclear. This study reveals that a brief, 5-min ultrasound (US) treatment of skeletal muscle robustly elevates circulating levels of muscle-derived EVs, introducing a novel, non-invasive stategy to modulate EV release. US-induced EVs showed altered miRNA profiles enriched with anti-inflammatory miRNAs that target pathways involved in inflammatory responses. Additionally, transient upregulation of reactive oxygen species and activation of the endoplasmic reticulum stress pathway were observed in US-treated muscle, suggesting a mechanism for enhanced EV release. Our findings establish US as the first non-invasive and rapid method to selectively enhance skeletal muscle-derived EV release into the circulation, highlighting its potential for therapeutic applications through its anti-inflammatory effect.</p>\n </div>","PeriodicalId":50455,"journal":{"name":"The FASEB Journal","volume":"39 13","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The FASEB Journal","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1096/fj.202501797R","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Skeletal muscle, the largest secretory organ, regulates distant organs through the secretion of various factors. Among these are extracellular vesicles (EVs), which play a significant role in mediating communication between muscle and other tissues and hold therapeutic potential due to their target specificity and anti-inflammatory properties. Enhancing the release of EVs from skeletal muscle into the circulation is crucial for eliciting their diverse effects, including anti-inflammatory actions; however, effective strategies to increase the levels of muscle-derived EVs in the bloodstream have not yet been developed. While exercise is the most studied method to increase blood EV levels, its efficacy in enhancing skeletal muscle-derived EVs remains unclear. This study reveals that a brief, 5-min ultrasound (US) treatment of skeletal muscle robustly elevates circulating levels of muscle-derived EVs, introducing a novel, non-invasive stategy to modulate EV release. US-induced EVs showed altered miRNA profiles enriched with anti-inflammatory miRNAs that target pathways involved in inflammatory responses. Additionally, transient upregulation of reactive oxygen species and activation of the endoplasmic reticulum stress pathway were observed in US-treated muscle, suggesting a mechanism for enhanced EV release. Our findings establish US as the first non-invasive and rapid method to selectively enhance skeletal muscle-derived EV release into the circulation, highlighting its potential for therapeutic applications through its anti-inflammatory effect.
期刊介绍:
The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.