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Fusion and beyond: Satellite cell contributions to loading-induced skeletal muscle adaptation
Open accessAbstract
Satellite cells support adult skeletal muscle fiber adaptations to loading in numerous ways. The fusion of satellite cells, driven by cell-autonomous and/or extrinsic factors, contributes new myonuclei to muscle fibers, associates with load-induced hypertrophy, and may support focal membrane damage repair and long-term myonuclear transcriptional output. Recent studies have also revealed that satellite cells communicate within their niche to mediate muscle remodeling in response to resistance exercise, regulating the activity of numerous cell types through various mechanisms such as secretory signaling and cell-cell contact. Muscular adaptation to resistance and endurance activity can be initiated and sustained for a period of time in the absence of satellite cells, but satellite cell participation is ultimately required to achieve full adaptive potential, be it growth, function, or proprioceptive coordination. While significant progress has been made in understanding the roles of satellite cells in adult muscle over the last few decades, many conclusions have been extrapolated from regeneration studies. This review highlights our current understanding of satellite cell behavior and contributions to adaptation outside of regeneration in adult muscle, as well as the roles of satellite cells beyond fusion and myonuclear accretion, which are gaining broader recognition.
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“Rather than acting as an obligatory requirement at all stages of hypertrophy, satellite cell fusion is better interpreted as a mechanism that becomes increasingly relevant when sustained loading pushes existing myonuclei toward their functional limits [22,68].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [68]
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“Once the initial gains supported by existing myonuclei have been largely realized, further adaptation may require a slower phase of structural remodeling involving satellite cell participation and myonuclear expansion [66,68].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [68]
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“Alternatively, emerging isolated single-fiber transcriptomics, which report absolute RNA content per isolated myofiber segment, entirely bypasses the tissue-denominator problem [68].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [68]
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“RNA:DNA is therefore not a universally superior method but a useful adjunct whose interpretation depends on the experimental question and timeframe [37,68].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [68]
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1 retracted
Pisconti, A., Brunelli, S., Padova, M. D., Palma, C. D., Deponti, D., Baesso, S., Sartorelli, V., Cossu, G., & Clementi, E. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200507083 · Cited by 107
RetractedSATELLITE CELL OF SKELETAL MUSCLE FIBERS
Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683
Pax7 Is Required for the Specification of Myogenic Satellite Cells
Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345
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Joe, A. W. B., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A., & Rossi, F. M. V. (2010) · Nature Cell Biology · doi:10.1038/ncb2015 · Cited by 1,690
Uezumi, A., Fukada, S., Yamamoto, N., Takeda, S., & Tsuchida, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2014 · Cited by 1,315
Murphy, M. M., Lawson, J. A., Mathew, S. J., Hutcheson, D. A., & Kardon, G. (2011) · Development · doi:10.1242/dev.064162 · Cited by 1,249
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Januel, L., Merlet, A. N., Hé, Z., Hourdé, C., Bartolucci, P., Gellen, B., Galactéros, F., Messonnier, L. A., & Féasson, L. (2022) · Journal of Histochemistry & Cytochemistry · doi:10.1369/00221554221103905 · Cited by 2
Muñoz López, M., López-Gil, J. F., Ramírez de la piscina Viúdez, X., Baz-Valle, E., & Tornero Aguilera, J. F. (2026) · Cells · doi:10.3390/cells15111041 · Cited by 1
“Rather than acting as an obligatory requirement at all stages of hypertrophy, satellite cell fusion is better interpreted as a mechanism that becomes increasingly relevant when sustained loading pushes existing myonuclei toward their functional limits [22,68].”
InfluentialADAPTIVE CHANGES OF THE CIRCULATORY SYSTEM IN STRENGTH SPORTS ATHLETES
Lyzohub, V., Rozova, K. V., Bakunovsky, O. M., Oliinyk, T. M., & Dubynska, S. M. (2023) · Bulletin of Problems Biology and Medicine · doi:10.29254/2077-4214-2023-3-170-56-64 · Cited by 1
Kim, B., Kim, D., Choi, Y., Kim, J., Heo, S.-H., & Park, S. (2024) · Food Science of Animal Resources · doi:10.5851/kosfa.2024.e82 · Cited by 1
Seldeen, K., Wang, N., Muthaiah, R., Treanor, O. P., Davis, A. L., Chaves, L., Thiyagarajan, R., Marzullo, B. J., Yergeau, D., & Troen, B. (2025) · Nutrients · doi:10.3390/nu17233733 · Cited by 1
GABA promotes myoblast fusion and prevents TNF-α-induced muscle protein degradation in C2C12 cells
Kusano, Y., Bando, H., Uyama, M., Miyamura, K., Miyake, T., & Shibata, T. (2025) · Food Science and Technology Research · doi:10.3136/fstr.fstr-d-25-00063 · Cited by 1
Tsai, C.-T., Hsu, C.-F., Murakami, R., Takagaki, Y., Uchibori, H., Kaneko, M., Hata, K., Kano, Y., & Osana, S. (2026) · Experimental Cell Research · doi:10.1016/j.yexcr.2026.115005 · Cited by 1
Jing, R., Pang, X., Zhu, X., Huang, S., & Gao, X. (2026) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2026.1863985 · Cited by 1
The Health Benefits of Exercise: Molecular and Cellular Mechanisms
Ying, P., Wang, H., Lu, X., Zhang, W., Lin, Z., Wang, K., Li, S., Chen, L., Jiang, M., Hamad, S., et al. (2026) · MedComm · doi:10.1002/mco2.70926 · Cited by 1
Scientific meeting report: International Biochemistry of Exercise 2022
Vainshtein, A., Slavin, M. B., Cheng, A. J., Memme, J. M., Oliveira, A. N., Perry, C. G. R., Sater, A. A. A., BELCASTRO, A. N., Riddell, M. C., Triolo, M., et al. (2022) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00475.2022 · Cited by 3
Bolado‐Carrancio, A., Tapia, O., & Rodríguez-Rey, J. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168800 · Cited by 2
Saugues, A., Kneppers, A. E. M., & Mounier, R. (2024) · médecine/sciences · doi:10.1051/medsci/2024133 · Cited by 1
Cumming, K. T., Elvatun, I. C., Kalenius, R., Divljak, G., Raastad, T., Psilander, N., & Horwath, O. (2025) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00353.2025 · Cited by 1
Transient MYC Mimicking the Exercise Response Orchestrates Multifaceted Skeletal Muscle AdaptationsPreprint
Jones, R. G., Koopmans, P. J., Serrano, N., Cabrera, A. R., Morena, F., Chambers, T. L., Walters, R., Borowik, A., Taylor, M. E., Wohlgemuth, R. P., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.29.735332 · Cited by 1
Self-citationGLUD1 dictates muscle stem cell differentiation by controlling mitochondrial glutamate levelsPreprint
Soro-Arnáiz, I., Cherkaoui, S., Fitzgerald, G., Zhang, J., Gilardoni, P. A., Ghosh, A., Bar‐Nur, O., Masschelein, E., Maechler, P., Zamboni, N., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.04.560525
Kim, B., Kim, D., Jo, Y., Choi, Y., Kim, J., Heo, S., & Park, S. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4669567
Alterations in Satellite Cell Differentiation from Young Patients with Cerebral Palsy
Stem Cell and Developmental Biology, D. O. D. A. R., Corvelyn, M., Costamagna, D., Stem Cell and Developmental Biology, D. O. D. A. R., Meirlevede, J., Stem Cell and Developmental Biology, D. O. D. A. R., Duelen, R., Stem Cell and Developmental Biology, D. O. D. A. R., Deschrevel, J., Gayan‐Ramirez, G., et al. (2023) · Physical Medicine and Rehabilitation - International · doi:10.26420/physmedrehabilint.2023.1217
The role of satellite cell-derived TRIM28 in mechanical load- and injury-induced myogenesisPreprint
Lin, K., Hibbert, J. E., Lemens, J. L., Torbey, M. M., Steinert, N. D., Flejsierowicz, P. M., Melka, K. M., Lares, M., Setaluri, V., & Hornberger, T. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.20.572566
MuSK-BMP signaling in adult muscle stem cells maintains quiescence and regulates myofiber sizePreprint
Madigan, L. A., Jaime, D., Chen, I., & Fallon, J. R. (2024) · eLife · doi:10.7554/elife.101078.1
MuSK-BMP signaling in adult muscle stem cells maintains quiescence and regulates myofiber sizePreprint
Madigan, L. A., Jaime, D., Chen, I., & Fallon, J. R. (2024) · eLife · doi:10.7554/elife.101078
Cumming, K. T., Elvatun, I. C., Kalenius, R., Divljak, G., Raastad, T., Psilander, N., & Horwath, O. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.28.650925
Park, J., Shim, S., & Hwang, N. (2025) · Gerodontology · doi:10.1111/ger.70024
Cabezas, F., Cabello‐Verrugio, C., González, N., Salas, J., Ramírez, M. J., de la Vega, E., & Olguín, H. C. (2024) · Figshare · doi:10.6084/m9.figshare.26587236
Cabezas, F., Cabello‐Verrugio, C., González, N., Salas, J., Ramírez, M. J., de la Vega, E., & Olguín, H. C. (2024) · Figshare · doi:10.6084/m9.figshare.26587227
Cabezas, F., Cabello‐Verrugio, C., González, N., Salas, J., Ramírez, M. J., de la Vega, E., & Olguín, H. C. (2024) · Figshare · doi:10.6084/m9.figshare.26587233
Metadata
- Authors
- Murach, K. A., Fry, C. S., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A.
- Affiliations
- University of Kentucky (US)
- Corresponding author
- Murach, Kevin A.
- Peterson, Charlotte A.
- ORCID
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 2021-09-04
- Volume
- 35
- Issue
- 10
- Pages
- e21893-e21893
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- PMC
- PMC9293230
- OpenAlex
- W3197320781
- Cited by
- 120
- References
- 234
- Citations by year
- 2026: 22 · 2025: 22 · 2024: 25 · 2023: 26 · 2022: 21 · 2021: 4
- FWCI
- 1.99
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- The FASEB Journal (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Journal of the Arkansas Academy of Science (submittedVersion, cc-by-nc)
- UKnowledge (University of Kentucky) (submittedVersion, cc-by-nc)
- Funders
- National Institutes of Health
- National Institute on Aging (AG049086, AG063994)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Health Sciences › Medicine › Physiology (medical) › Exercise and Physiological Responses
- Keywords
- satellite cells, skeletal muscle adaptation, myonuclear accretion, muscle hypertrophy, resistance training, endurance exercise, muscle remodeling, extrinsic signaling, cell-cell contact, proprioception, muscle regeneration
- MeSH terms
- Adaptation, Physiological, Animals, Humans, Signal Transduction, Muscle Fibers, Skeletal, Satellite Cells, Skeletal Muscle
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