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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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]
Citations
Cites
Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors
Takahashi, K., Tanabe, K., Ohnuki, M., Narita, M., Ichisaka, T., Tomoda, K., & Yamanaka, S. (2007) · Cell · doi:10.1016/j.cell.2007.11.019 · Cited by 20,221
Embryonic Stem Cell Lines Derived from Human Blastocysts
Thomson, J. A., Itskovitz‐Eldor, J., Shapiro, S. S., Waknitz, M. A., Swiergiel, J. J., Marshall, V. S., & Jones, J. M. (1998) · Science · doi:10.1126/science.282.5391.1145 · Cited by 15,947
Matrix elasticity directs stem cell lineage specification
Engler, A. J., Sen, S., Sweeney, H. L., & Discher, D. E. (2006) · Cell · doi:10.1016/j.cell.2006.06.044 · Cited by 13,915
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766
SATELLITE CELL OF SKELETAL MUSCLE FIBERS
Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683
The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation
Chen, J., Mandel, E. M., Thomson, J. M., Wu, Q., Callis, T. E., Hammond, S. M., Conlon, F. L., & Wang, D.-Z. (2005) · Nature Genetics · doi:10.1038/ng1725 · Cited by 2,807
Rejuvenation of aged progenitor cells by exposure to a young systemic environment
Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287
Satellite Cells and the Muscle Stem Cell Niche
Yin, H., Price, F., & Rudnicki, M. A. (2013) · Physiological Reviews · doi:10.1152/physrev.00043.2011 · Cited by 2,166
Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., van Rooijen, N., Plonquet, A., Gherardi, R. K., & Chazaud, B. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070075 · Cited by 2,002
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
Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
de Morrée, A., & Rando, T. A. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00568-6 · Cited by 258
Multimodal cell atlas of the ageing human skeletal muscle
Lai, Y., Ramírez‐Pardo, I., Isern, J., An, J., Perdiguero, E., Serrano, A. L., Li, J., García-Domínguez, E., Segalés, J., Guo, P.-C., et al. (2024) · Nature · doi:10.1038/s41586-024-07348-6 · Cited by 247
Self-citationHong, X., Isern, J., Campanario, S., Perdiguero, E., Ramírez-Pardo, I., Segalés, J., Hernansanz-Agustín, P., Curtabbi, A., Deryagin, O., Pollán, A., et al. (2022) · Cell stem cell · doi:10.1016/j.stem.2022.07.009 · Cited by 213
Self-citationSarcopenic obesity: Emerging mechanisms and therapeutic potential
Axelrod, C. L., Dantas, W. S., & Kirwan, J. P. (2023) · Metabolism · doi:10.1016/j.metabol.2023.155639 · Cited by 204
Bioelectronics for electrical stimulation: materials, devices and biomedical applications
Huang, Y., Yao, K., Zhang, Q., Huang, X., Chen, Z., Zhou, Y., & Yu, X. (2024) · Chemical Society Reviews · doi:10.1039/d4cs00413b · Cited by 168
Gasdermin D-mediated metabolic crosstalk promotes tissue repair
Chi, Z., Chen, S., Yang, D., Cui, W., Lu, Y., Wang, Z., Li, M., Yu, W., Zhang, J., Jiang, Y., et al. (2024) · Nature · doi:10.1038/s41586-024-08022-7 · Cited by 116
Granic, A., Suetterlin, K., Shavlakadze, T., Grounds, M. D., & Sayer, A. A. (2023) · Clinical Science · doi:10.1042/cs20230319 · Cited by 124
Cellular Senescence and Ageing: Mechanisms and Interventions
Mylonas, A., & O’Loghlen, A. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.866718 · Cited by 114
A stem cell aging framework, from mechanisms to interventions
Liu, B., Qu, J. T., Zhang, W., Belmonte, J. C. I., & Liu, G. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111451 · Cited by 110
Huang, Y., Li, H., Hu, T., Li, J., Yiu, C. K., Zhou, J., Li, J., Huang, X., Yao, K., Qiu, X., et al. (2022) · Nano Letters · doi:10.1021/acs.nanolett.2c01997 · Cited by 102
Liu, Y., Wang, R., Ding, S., Deng, L., Zhang, Y., Li, J., Shi, Z., Wu, Z., Liang, K., Yan, X., et al. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121615 · Cited by 101
Energy metabolism as therapeutic target for aged wound repair by engineered extracellular vesicle
Zhuang, Y., Jiang, S., Deng, X., Lao, A., Hua, X., Xie, Y., Jiang, L., Wang, X., & Lin, K. (2024) · Science Advances · doi:10.1126/sciadv.adl0372 · Cited by 91
A neuromuscular perspective of sarcopenia pathogenesis: deciphering the signaling pathways involved
Moreira-Pais, A., Ferreira, R., Oliveira, P. A., & Duarte, J. A. (2022) · GeroScience · doi:10.1007/s11357-021-00510-2 · Cited by 74
Pathological and Inflammatory Consequences of Aging
García‐Domínguez, M. (2025) · Biomolecules · doi:10.3390/biom15030404 · Cited by 78
The association of lipid metabolism and sarcopenia among older patients: a cross-sectional study
Jiang, Y., Xu, B., Zhang, K., Zhu, W., Lian, X., Xu, Y., Chen, Z., Liu, L., & Guo, Z. (2023) · Scientific Reports · doi:10.1038/s41598-023-44704-4 · Cited by 74
Stem cell aging in the skeletal muscle: The importance of communication
Hong, X., Campanario, S., Ramírez‐Pardo, I., Grima-Terrén, M., Isern, J., & Muñoz‐Cánoves, P. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101528 · Cited by 73
Self-citationEmerging Targets and Treatments for Sarcopenia: A Narrative Review
Cacciatore, S., Calvani, R., Esposito, I., Massaro, C., Gava, G., Picca, A., Tosato, M., Marzetti, E., & Landi, F. (2024) · Nutrients · doi:10.3390/nu16193271 · Cited by 75
Lloyd, E. M., Pinniger, G. J., Murphy, R. M., & Grounds, M. D. (2023) · Acta Physiologica · doi:10.1111/apha.14012 · Cited by 67
Hou, Y., Xiang, J., Wang, B., Duan, S., Song, R., Zhou, W., Tan, S., & He, B. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1263650 · Cited by 72
Ma, L., Meng, Y., An, Y., Han, P., Zhang, C., Yue, Y., Wen, C., Shi, X., Jin, J., Yang, G., et al. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13484 · Cited by 66
Mechanisms of muscle cells alterations and regeneration decline during aging
Chinvattanachot, G., Rivas, D., & Duque, G. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102589 · Cited by 61
Post‐translational regulation of muscle growth, muscle aging and sarcopenia
Zhong, Q., Zheng, K., Li, W., An, K., Liu, Y., Xiao, X., Hai, S., Dong, B., Li, S., An, Z., et al. (2023) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13241 · Cited by 59
Southerland, K. W., Xu, Y., Peters, D., Wei, X., Lin, X., Xiang, Y., Fei, K., Olivere, L. A., Morowitz, J. M., Otto, J. C., et al. (2023) · Genome Medicine · doi:10.1186/s13073-023-01250-y · Cited by 56
Wireless Battery-free and Fully Implantable Organ Interfaces
Bhatia, A., Hanna, J., Stuart, T., Kasper, K. A., Clausen, D. M., & Gutruf, P. (2024) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00425 · Cited by 50
MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury
Jiang, H., Liu, B., Lin, J., Xue, T., Han, Y., Lu, C., Zhou, S., Gu, Y., Xu, F., Shen, Y., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05096-w · Cited by 53
Fernández‐Lázaro, D., Garrosa, E., Seco‐Calvo, J., & Garrosa, M. (2022) · Proteomes · doi:10.3390/proteomes10030029 · Cited by 49
Advances in sarcopenia: mechanisms, therapeutic targets, and intervention strategies
Zheng, Y., Feng, J., Yu, Y., Ling, M., & Wang, X. (2024) · Archives of Pharmacal Research · doi:10.1007/s12272-024-01493-2 · Cited by 46
Huang, Y., Wang, C., Cui, H., Sun, G., Qi, X., & Yao, X. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1590524 · Cited by 54
Immunometabolism of macrophages regulates skeletal muscle regeneration
Chen, Y.-F., Lee, C., Wu, H.-H., Lin, W., & Lee, O. K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.948819 · Cited by 46
The multifaceted role of macrophages in homeostatic and injured skeletal muscle
Wang, X., & Zhou, L. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1274816 · Cited by 45
Zhou, S., Li, Z., Li, X., Ye, Y., Wang, M., Jiang, J., Tao, L., Wang, Y., Tung, C.-T., ., Y. C., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.05.006 · Cited by 50
Glutamine Metabolism Is Required for Alveolar Regeneration during Lung Injury
Wang, S., Li, X., Ma, Q., Wang, Q., Wu, J., Yu, H., Li, K., Li, Y., Wang, J., Zhang, Q., et al. (2022) · Biomolecules · doi:10.3390/biom12050728 · Cited by 40
Endo, T. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.09.048 · Cited by 44
Aging disrupts MANF-mediated immune modulation during skeletal muscle regeneration
Sousa, N. S., Brás, M. F., Antunes, I. B., Lindholm, P., Neves, J., & Sousa‐Victor, P. (2023) · Nature Aging · doi:10.1038/s43587-023-00382-5 · Cited by 40
Self-citationRegenerating Myofibers after an Acute Muscle Injury: What Do We Really Know about Them?
Pizza, F. X., & Buckley, K. H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612545 · Cited by 37
Zhang, S., Yang, F., Huang, Y., He, L., Li, Y., Wan, Y. C. E., Ding, Y., Chan, K. M., Xie, T., Sun, H., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40465-w · Cited by 36
Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD
Mázala, D. A. G., Hindupur, R., Moon, Y. J., Shaikh, F., Gamu, I. H., Alladi, D., Panci, G., Weiss‐Gayet, M., Chazaud, B., Partridge, T. A., et al. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01503-0 · Cited by 34
The muscle stem cell niche at a glance
Hung, M., Lo, H.-F., Jones, G. E. L., & Krauss, R. S. (2023) · Journal of Cell Science · doi:10.1242/jcs.261200 · Cited by 38
Transplanting rejuvenated blood stem cells extends lifespan of aged immunocompromised mice
Montserrat‐Vazquez, S., Ali, N., Matteini, F., Lozano-Bartolomé, J., Tu, Z., Mejía-Ramírez, E., Marka, G., Vollmer, A., Soller, K., Saçma, M., et al. (2022) · npj Regenerative Medicine · doi:10.1038/s41536-022-00275-y · Cited by 38
Wang, C., Zhao, B., Zhai, J., Wang, A., Cao, N., Liao, T., Su, R., He, L., Li, Y., Pei, X., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05843-8 · Cited by 35
Psat1-generated α-ketoglutarate and glutamine promote muscle stem cell activation and regenerationPreprint
Ciuffoli, V., Feng, X., Jiang, K., Acevedo-Luna, N., Ko, K. D., Wang, A. H. J., Riparini, G., Khateb, M., Glancy, B. C., Dell’Orso, S., et al. (2024) · Genes & Development · doi:10.1101/gad.351428.123 · Cited by 38
Exploring cellular senescence in the musculoskeletal system: Any insights for biomarkers discovery?
Gerosa, L., Malvandi, A. M., Malavolta, M., Provinciali, M., & Lombardi, G. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101943 · Cited by 33
Cellular interactions and microenvironment dynamics in skeletal muscle regeneration and disease
Rodríguez, C., Timóteo-Ferreira, F., Minchiotti, G., Brunelli, S., & Guardiola, O. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1385399 · Cited by 36
Adult stem cell sources for skeletal and smooth muscle tissue engineering
Salemi, S., Prange, J. A., Baumgartner, V., Haralampieva, D., & Eberli, D. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02835-x · Cited by 32
Guo, Q., Luo, Q., & Song, G. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13440 · Cited by 35
Chen, S., Huang, L., Liu, B., Duan, H., Li, Z., Liu, Y., Li, H., Fu, X., Lin, J., Xu, Y., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2400-3 · Cited by 36
Wang, J., Li, D., Zheng, L.-F., Ren, S., Huang, Z.-Q., Tao, Y., Liu, Z., Shang, Y., Pang, D., Guo, H., et al. (2024) · Developmental Cell · doi:10.1016/j.devcel.2023.12.005 · Cited by 31
Sarcopenia: how to determine and manage
Chung, J. Y., Kim, S., Kim, S. H., & Park, C. H. (2025) · Knee Surgery and Related Research · doi:10.1186/s43019-025-00265-6 · Cited by 32
Li, F., Zhang, F., Shi, H., Xia, H., Wei, X., Liu, S., Wu, T., Li, Y., Feng, S., Chen, M., et al. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13526 · Cited by 28
Three‐dimensional chromatin re‐organization during muscle stem cell aging
Yang, B. A., Larouche, J. A., Sabin, K., Fraczek, P. M., Parker, S. C. J., & Aguilar, C. A. (2023) · Aging Cell · doi:10.1111/acel.13789 · Cited by 27
Nolt, G. L., Keeble, A. R., Wen, Y., Strong, A. C., Thomas, N. T., Valentino, T. R., Brightwell, C. R., Murach, K. A., Patrizia, S., Weinstabl, H., et al. (2023) · GeroScience · doi:10.1007/s11357-023-00976-2 · Cited by 27
Gli1 marks a sentinel muscle stem cell population for muscle regeneration
Peng, J., Han, L., Liu, B., Song, J., Wang, Y., Wang, K., Guo, Q., Liu, X., Li, Y., Zhang, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42837-8 · Cited by 28
The immune landscape of murine skeletal muscle regeneration and aging
Sousa, N. S., Bica, M., Brás, M. F., Sousa, A. C., Antunes, I. B., Encarnação, I. A., Costa, T. M., Martins, I. B., Barbosa‐Morais, N. L., Sousa‐Victor, P., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114975 · Cited by 30
Self-citationLicochalcone A and B enhance muscle proliferation and differentiation by regulating Myostatin
Ahmad, K., Lee, E. J., Ali, S. M., Han, K. S., Hur, S. J., Lim, J. H., & Choi, I. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155350 · Cited by 26
From molecular to physical function: The aging trajectory
Janssen, T., Lowisz, C. V., & Phillips, S. M. (2024) · Current Research in Physiology · doi:10.1016/j.crphys.2024.100138 · Cited by 31
Perspectives on mitochondrial dysfunction in the regeneration of aging skeletal muscle
Wang, K., Gan, M., Lei, Y., Liao, T., Li, J., Niu, L., Zhao, Y., Chen, L., Wang, Y., Zhu, L., et al. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00771-1 · Cited by 34
Ancel, S., Michaud, J., Migliavacca, E., Jomard, C., Fessard, A., Garcia, P., Karaz, S., Raja, S., Jacot, G. E., Desgeorges, T., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci163648 · Cited by 25
Zhang, Z., Lin, S., Luo, W., Ren, T., Huang, X., Li, W., & Zhang, X. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911327 · Cited by 25
Yin, P., Chen, M., Rao, M., Lin, Y., Zhang, M., Xu, R., Hu, X., Chen, R., Chai, W., Huang, X., et al. (2023) · Advanced Science · doi:10.1002/advs.202304084 · Cited by 29
Zhang, L., Ge, Y., Zhao, W., Shu, X., Kang, L., Wang, Q., & Liu, Y. (2025) · Journal of Medical Internet Research · doi:10.2196/67846 · Cited by 29
Riparini, G., Mackenzie, M. E., Naz, F., Brooks, S. R., Jiang, K., Deewan, A., Dulek, B., Islam, S., Ko, K. D., Tsai, W. L., et al. (2025) · Nature Aging · doi:10.1038/s43587-025-01002-0 · Cited by 27
Decline of regenerative potential of old muscle stem cells: contribution to muscle aging
Sahinyan, K., Lazure, F., Blackburn, D. M., & Soleimani, V. D. (2022) · FEBS Journal · doi:10.1111/febs.16352 · Cited by 25
Muscle is a stage, and cells and factors are merely players
Roman, W., & Muñoz‐Cánoves, P. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.03.001 · Cited by 25
Self-citationWang, T., Xu, H. Y., Wu, S., Guo, Y., Zhao, G., & Wang, D. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c02023 · Cited by 28
Skrivergaard, S., Rasmussen, M. K., Sahebekhtiari, N., Young, J. F., & Therkildsen, M. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113217 · Cited by 24
Mechanisms of the NAD+ salvage pathway in enhancing skeletal muscle function
Su, M., Qiu, F., Li, Y., Che, T., Li, N., & Zhang, S. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1464815 · Cited by 27
Huang, N., Ge, M., Liu, X., Tian, X., Yin, P., Bao, Z., Cao, F., Shyh‐Chang, N., Dong, B., Dai, L., et al. (2024) · Life Medicine · doi:10.1093/lifemedi/lnaf001 · Cited by 27
Li, N., Chen, Y., Wang, Q., Liu, X., Han, C., Qu, C., Guan, X., Zou, W., Wang, X., Li, A., et al. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04481-5 · Cited by 26
Lipocalin 2—A bone‐derived anorexigenic and β‐cell promoting signal: From mice to humans
Yang, Y., Liu, J., & Kousteni, S. (2023) · Journal of Diabetes · doi:10.1111/1753-0407.13504 · Cited by 22
The roles of media ingredients in muscle cell culture for cultured meat production—A mini-review
Lee, D.-Y., Yun, S. H., Lee, J., Mariano, E., Choi, Y., Han, D., Park, J., Kim, J. S., Lee, S.-Y., & Hur, S. (2024) · Future Foods · doi:10.1016/j.fufo.2024.100403 · Cited by 25
FAPs orchestrate homeostasis of muscle physiology and pathophysiology
Yin, K., Zhang, C., Deng, Z., Wei, X., Xiang, T., Yang, C. H., Chen, C., Chen, Y., & Luo, F. (2024) · The FASEB Journal · doi:10.1096/fj.202400381r · Cited by 22
Jacques, E., Kuang, Y., Kann, A. P., Grand, F. L., Krauss, R. S., & Gilbert, P. M. (2022) · eLife · doi:10.7554/elife.81738 · Cited by 22
Hao, J., Zhuang, Z., Hu, S.-Y., Zhang, Y., Zhang, J.-W., He, F.-J., Wang, R., Zhuang, W., & Wang, M. (2024) · Lipids in Health and Disease · doi:10.1186/s12944-024-02243-5 · Cited by 22
The role of AGEs in muscle ageing and sarcopenia
Guo, Z.-J., Li, H., Jiang, S., Rahmati, M., Su, J., Yang, S., Wu, Y., Li, Y., & Deng, Z. (2025) · Bone and Joint Research · doi:10.1302/2046-3758.143.bjr-2024-0252.r1 · Cited by 21
Gold nanoparticles modulate macrophage polarization to promote skeletal muscle regeneration
Xu, L., Qiu, J., Ren, Q., Wang, D., Guo, A., Wang, L., Hou, K., Wang, R., & Liu, Y. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.101653 · Cited by 21
Skeletal Muscle Complications in Chronic Kidney Disease
Troutman, A. D., Arroyo, E., Lim, K. J., Moorthi, R. N., & Avin, K. G. (2022) · Current Osteoporosis Reports · doi:10.1007/s11914-022-00751-w · Cited by 22
Muscle stem cells get a new look: Dynamic cellular projections as sensors of the stem cell niche
Krauss, R. S., & Kann, A. P. (2023) · BioEssays · doi:10.1002/bies.202200249 · Cited by 20
Zuo, M., Fang, J., Huang, P., Liu, S., Hou, P., Wang, S., Liu, Z., Feng, C., Cao, L., Li, P., et al. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01568-x · Cited by 22
The roles of miRNAs in adult skeletal muscle satellite cells
Koopmans, P. J., Ismaeel, A., Goljanek‐Whysall, K., & Murach, K. A. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.10.403 · Cited by 22
Chen, J., Chen, H., Dong, X., Hui, T., Yan, M., Ren, D., Zou, S., Wang, S., Fei, E., Zhang, W., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06581-1 · Cited by 24
Borba, V. Z. C., & Costa, T. M. D. R. L. (2024) · Archives of Endocrinology and Metabolism · doi:10.20945/2359-4292-2024-0084 · Cited by 21
Duan, H., Chen, S., Mai, X., Fu, L., Huang, L., Xiao, L., Liao, M., Chen, H., Liu, G., & Xie, L. (2024) · Cellular Signalling · doi:10.1016/j.cellsig.2024.111097 · Cited by 20
Koike, H., Sugimura, M., Ouchi, R., Yoshimoto, Y., Manabe, I., & Oishi, Y. (2025) · Aging Cell · doi:10.1111/acel.70042 · Cited by 22
Immune aging impairs muscle regeneration via macrophage-derived anti-oxidant selenoprotein P
Hoang, D.-H., Bouvière, J., Galvis, J., Moullé, P., Mercier, O., Migliavacca, E., Ghosh, A., Juban, G., Liot, S., Stuelsatz, P., et al. (2025) · EMBO Reports · doi:10.1038/s44319-025-00516-3 · Cited by 21
Anti-inflammatory therapy enables robot-actuated regeneration of aged muscle
McNamara, S. L., Seo, B. R., Freedman, B. R., Roloson, E. B., Alvarez, J. T., O’Neill, C., Vandenburgh, H. H., Walsh, C. J., & Mooney, D. J. (2023) · Science Robotics · doi:10.1126/scirobotics.add9369 · Cited by 22
He, P., Du, G., Qin, X., & Li, Z. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121619 · Cited by 21
VEGFA Promotes Skeletal Muscle Regeneration in Aging
Endo, Y., Hwang, C. D., Zhang, Y., Olumi, S., Koh, D. J., Zhu, C., Neppl, R. L., Agarwal, S., & Sinha, I. (2023) · Advanced Biology · doi:10.1002/adbi.202200320 · Cited by 20
Zhang, Y., Wang, L., Kang, H., Lin, C.-Y. J., & Fan, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076551 · Cited by 21
Polyamines and Physical Activity in Musculoskeletal Diseases: A Potential Therapeutic Challenge
Galasso, L., Cappella, A., Mulè, A., Castelli, L., Ciorciari, A. M., Stacchiotti, A., & Montaruli, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129798 · Cited by 25
Alternations of NF-κB Signaling by Natural Compounds in Muscle-Derived Cancers
Radzka, J., Łapińska, Z., Szwedowicz, U., Gajewska-Naryniecka, A., Gizak, A., & Kulbacka, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241511900 · Cited by 20
Extra-osseous Roles of the RANK-RANKL-OPG Axis with a Focus on Skeletal Muscle
Gostage, J., Kostenuik, P. J., Goljanek‐Whysall, K., Bellantuono, I., McCloskey, E. V., & Bonnet, N. (2024) · Current Osteoporosis Reports · doi:10.1007/s11914-024-00890-2 · Cited by 21
NAD+: An old but promising therapeutic agent for skeletal muscle ageing
Xu, Y., & Xiao, W. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102106 · Cited by 20
Abdalla, B. A., Xiong, X., Chai, X., Xu, Q., Gong, J., & Xu, J. (2024) · International Journal of Biological Sciences · doi:10.7150/ijbs.96885 · Cited by 20
A Long Journey before Cycling: Regulation of Quiescence Exit in Adult Muscle Satellite Cells
Zhou, S., Han, L., & Wu, Z. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031748 · Cited by 21
Dowling, P., Swandulla, D., & Ohlendieck, K. (2023) · European Journal of Translational Myology · doi:10.4081/ejtm.2023.11856 · Cited by 18
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review