Abstract
Background Skeletal muscle (SkM) is a large, secretory organ that produces and releases myokines that can have autocrine, paracrine, and endocrine effects. Whether extracellular vesicles (EVs) also play a role in the SkM adaptive response and ability to communicate with other tissues is not well understood. The purpose of this study was to investigate EV biogenesis factors, marker expression, and localization across cell types in the skeletal muscle. We also aimed to investigate whether EV concentrations are altered by disuse atrophy.
Methods To identify the potential markers of SkM‑derived EVs, EVs were isolated from rat serum using density gradient ultracentrifugation, followed by fluorescence correlation spectroscopy measurements or qPCR. Single‑cell RNA sequencing (scRNA‑seq) data from rat SkM were analyzed to assess the EV biogenesis factor expression, and cellular localization of tetraspanins was investigated by immunohistochemistry. Finally, to assess the effects of mechanical unloading on EV expression in vivo, EV concentrations were measured in the serum by nanoparticle tracking analysis in both a rat and human model of disuse.
Results In this study, we show that the widely used markers of SkM‑derived EVs, α‑sarcoglycan and miR‑1, are undetectable in serum EVs. We also found that EV biogenesis factors, including the tetraspanins CD63, CD9, and CD81, are expressed by a variety of cell types in SkM. SkM sections showed very low detection of CD63, CD9, and CD81 in myofibers and instead accumulation within the interstitial space. Furthermore, although there were no differences in serum EV concentrations following hindlimb suspension in rats, serum EV concentrations were elevated in human subjects after bed rest.
Conclusions Our findings provide insight into the distribution and localization of EVs in SkM and demonstrate the importance of methodological guidelines in SkM EV research.
Document Type
Article
Publication Date
2023
Digital Object Identifier (DOI)
https://doi.org/10.1186/s13395-023-00315-1
Funding Information
This work was supported by the National Center for Complementary and Integrative Health, National Institutes of Health grant R01AT009268 (EED, TAB); National Institute on Aging, National Institutes of Health grant R01AG050781 (MJD); and National Institute on Aging, National Institutes of Health grant F99AG073493 (JJP). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Repository Citation
Ismaeel, Ahmed; Van Pelt, Douglas W.; Hettinger, Zachary; Fu, Xu; Richards, Christopher I.; Butterfield, Timothy A.; Petrocelli, Jonathan J.; Vechetti, Ivan J. Jr.; Confides, Amy L.; Drummond, Micah J.; and Dupont-Versteegden, Esther E., "Extracellular vesicle distribution and localization in skeletal muscle at rest and following disuse atrophy" (2023). Markey Cancer Center Faculty Publications. 336.
https://uknowledge.uky.edu/markey_facpub/336
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Notes/Citation Information
© The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.