The DOI matches its Crossref record; 297 of the 299 references it cites were found in a registry or an index.
Control of satellite cell function in muscle regeneration and its disruption in ageing
Abstract
Skeletal muscle contains a designated population of adult stem cells, called satellite cells, which are generally quiescent. In homeostasis, satellite cells proliferate only sporadically and usually by asymmetric cell division to replace myofibres damaged by daily activity and maintain the stem cell pool. However, satellite cells can also be robustly activated upon tissue injury, after which they undergo symmetric divisions to generate new stem cells and numerous proliferating myoblasts that later differentiate to muscle cells (myocytes) to rebuild the muscle fibre, thereby supporting skeletal muscle regeneration. Recent discoveries show that satellite cells have a great degree of population heterogeneity, and that their cell fate choices during the regeneration process are dictated by both intrinsic and extrinsic mechanisms. Extrinsic cues come largely from communication with the numerous distinct stromal cell types in their niche, creating a dynamically interactive microenvironment. This Review discusses the role and regulation of satellite cells in skeletal muscle homeostasis and regeneration. In particular, we highlight the cell-intrinsic control of quiescence versus activation, the importance of satellite cell-niche communication, and deregulation of these mechanisms associated with ageing. The increasing understanding of how satellite cells are regulated will help to advance muscle regeneration and rejuvenation therapies.
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“Tissue regeneration requires coordination between resident stem cells and local niche cells1,2.”
From Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration (2023) · cites this paper as [2]
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Cites
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Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
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SATELLITE CELL OF SKELETAL MUSCLE FIBERS
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The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation
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Cited by
Sorted by citations
Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration
Moiseeva, V., Cisneros, A., Sica, V., Deryagin, O., Lai, Y., Jung, S., Andrés, E., An, J., Segalés, J., Ortet, L., et al. (2023) · Nature · doi:10.1038/s41586-022-05535-x · Cited by 423
Self-citationCai, Y., Song, W., Li, J., Jing, Y., Liang, C., Zhang, L., Zhang, X., Zhang, W., Liu, B., An, Y., et al. (2022) · Science China Life Sciences · doi:10.1007/s11427-022-2161-3 · Cited by 450
Bao, H., Cao, J., Chen, M., Min, C., Chen, W., Chen, X., Chen, Y., Chen, Y., Chen, Y., Chen, Z., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2305-0 · Cited by 402
Healthcare on the brink: navigating the challenges of an aging society in the United States
Jones, C. H., & Dolsten, M. (2024) · npj Aging · doi:10.1038/s41514-024-00148-2 · Cited by 439
Bilski, J., Pierzchalski, P., Szczepanik, M., Bonior, J., & Zoladz, J. A. (2022) · Cells · doi:10.3390/cells11010160 · Cited by 271
Metadata
- Authors
- Sousa-Victor, P., García-Prat, L., & Muñoz-Cánoves, P.
- ORCID
- Muñoz-Cánoves, Pura
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2021-10-18
- Volume
- 23
- Issue
- 3
- Pages
- 204-226
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- OpenAlex
- W3205354997
- Cited by
- 476
- References
- 299
- Citations by year
- 2026: 107 · 2025: 126 · 2024: 118 · 2023: 78 · 2022: 45 · 2021: 2
- FWCI
- 6.48
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion)
- Funders
- Canadian Institutes of Health Research (201910MFE-430959-284655)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- satellite cells, skeletal muscle regeneration, muscle aging, muscle stem cells, quiescence, cell activation, asymmetric cell division, symmetric cell division, myogenesis, stem cell niche, niche microenvironment, stromal cells, muscle homeostasis, cell-intrinsic regulation
- MeSH terms
- Cell Differentiation, Stem Cells, Muscle, Skeletal, Satellite Cells, Skeletal Muscle
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