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
Items 301–400 of 480
Aging Larynx: Molecular and Cellular Aspect
Jung, S. Y. (2024) · Journal of The Korean Society of Laryngology Phoniatrics and Logopedics · doi:10.22469/jkslp.2024.35.1.6 · Cited by 2
Macrophage scavenger receptor A1 promotes skeletal muscle regeneration after hindlimb ischemia
Wang, S., Wang, S., Cai, W., Wang, J., Huang, J., Yang, Q. K., Bai, H., Jiang, B., Ben, J., Zhang, H., et al. (2024) · Journal of Biomedical Research · doi:10.7555/jbr.38.20240117 · Cited by 2
Isolation of a persistently quiescent muscle satellite cell population
Steele, A. P., Syroid, A. L., Mombo, C., Raveetharan, S., Rebalka, I. A., & Hawke, T. J. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00231.2024 · Cited by 2
Yozgatlı, T. K., Dolanbay, E. G., Cingoz, T., Paksoy, A. E., Uslu, Ü., Ovalı, E., & Kocaoğlu, B. (2024) · Journal of Experimental Orthopaedics · doi:10.1002/jeo2.12087 · Cited by 2
Overexpression of CPT1A disrupts the maintenance and regenerative function of muscle stem cells
Qiu, J., Yue, F., Kim, K. H., Chen, X., Khedr, M. A., Chen, J., Gu, L., Ren, J., Ferreira, C. R., Ellis, J. M., et al. (2024) · The FASEB Journal · doi:10.1096/fj.202400947r · Cited by 4
Zhang, J., Qu, S., Huang, Y., Zhang, X., Tong, X.-B., Fang, Y.-P., Rao, T., Liu, K., Jia, L., Lin, Y., et al. (2024) · Journal of Pain Research · doi:10.2147/jpr.s475942 · Cited by 2
An adult myogenic cell line of the Japanese fire-bellied newt Cynops pyrrhogaster
Shiga, S., Murakami, Y., Wang, Z., Andõ, R., Casco‐Robles, M. M., Maruo, F., Toyama, F., & Chiba, C. (2024) · Scientific Reports · doi:10.1038/s41598-024-81899-6 · Cited by 2
Arginase-II gene deficiency reduces skeletal muscle aging in mice
Caretti, M., Potenza, D. M., Ajalbert, G., Albrecht, U., Ming, X., Brenna, A., & Yang, Z. (2024) · Aging · doi:10.18632/aging.206173 · Cited by 2
PIEZO1 activation enhances myogenesis and mitigates muscle degeneration in rotator cuff tear
Wang, T., Feng, S., Zhou, H., Mao, W., Bai, R., Xia, Y., Huang, J., Zhang, R., & Lin, F. (2024) · Regenerative Therapy · doi:10.1016/j.reth.2024.12.002 · Cited by 3
The role of primary cilia in myoblast proliferation and cell cycle regulation during myogenesis
Wu, Z., Chen, N., & Takao, D. (2025) · Cell Structure and Function · doi:10.1247/csf.24067 · Cited by 2
Increased Matrix Stiffness Promotes Slow Muscle Fibre Regeneration After Skeletal Muscle Injury
Wang, D., Wu, J., Xu, Z., Jia, J.-N., Lai, Y., & He, Z. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70423 · Cited by 5
Matsuyama, T., PASANEN, S., FUTAMI, F., Ayari, K. A. T. O., Hirata, I., Yanamoto, S., & Kato, K. (2025) · Dental Materials Journal · doi:10.4012/dmj.2024-314 · Cited by 2
Shi, R., Chen, G., Zhang, Y., Zhang, J., Lu, Y., & Duan, Y. (2025) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-025-09694-y · Cited by 3
Kolonay, D., Grueter, C. E., & Baskin, K. K. (2025) · Journal of Molecular and Cellular Cardiology Plus · doi:10.1016/j.jmccpl.2025.100456 · Cited by 3
Apol9a regulates myogenic differentiation via the ERK1/2 pathway in C2C12 cells
Jiang, X. J., Ji, S., Cui, S., Wang, R., Wang, W., Chen, Y. Q., & Zhu, S. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.942061 · Cited by 2
Gerosa, L., Malvandi, A. M., Gomarasca, M., Verdelli, C., Sansoni, V., Faraldi, M., Ziemann, E., Olivieri, F., Banfi, G., & Lombardi, G. (2024) · The Journals of Gerontology Series A · doi:10.1093/gerona/glae022 · Cited by 2
mRNA transcription in skeletal muscle drives growth and determines nuclear accretionPreprint
Montecino, F., Calvo, C., Swoboda, C. O., Bruening, A. S., Cramer, A., Lin, X., Martin, J. L., Khairallah, R. J., Diao, Y., Prasad, V., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.29.696842 · Cited by 2
Ahmad, S. S., & Choi, I. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24942 · Cited by 1
Effect of NR1D1 on the proliferation and differentiation of yak skeletal muscle satellite cells
Zhe, Y., Wu, Z., Yasenjian, S., Zhong, J., Jiang, H., Zhang, M., Chai, Z., & Xin, J. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1428117 · Cited by 1
Lu, Y., Xu, K., Kong, J., & Liu, C. (2025) · Molecular & cellular biomechanics · doi:10.62617/mcb1298 · Cited by 1
Zuo, W., Peng, J., Guo, W., & Wu, J. (2025) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2025.105788 · Cited by 1
HDAC11 deficiency regulates age-related muscle decline and sarcopenia
Odria, R., Cardús, A., Gomis-Coloma, C., Balanyà-Segura, M., Mercado-Amarilla, A., Maestre-Mora, P., Sabuco, A. P., Domingo, J. C., Nogales‐Gadea, G., Gomez-Sanchez, J. A., et al. (2025) · GeroScience · doi:10.1007/s11357-025-01611-y · Cited by 1
Update on Treatment of Dystrophinopathy
Keselman, D. J., & Brandsema, J. F. (2025) · Current Treatment Options in Neurology · doi:10.1007/s11940-025-00841-x · Cited by 1
Cellular Senescence in Skeletal Muscle: Age, Sarcopenia, Therapy
Плехова, Н. Г., Андреевна, Н. П., Voro, A. N., Korolev, D. V., & Шуматов, В. Б. (2025) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093025030147 · Cited by 1
Wang, X., Wang, Q., Wang, Z., Zhou, Y., Jiang, X., & Li, Y. (2025) · Biological Research · doi:10.1186/s40659-025-00634-1 · Cited by 1
Evaluating the potential of graphene oxide to promote skeletal muscle complex regeneration
Chen, Y., Zhu, Z., Shen, Y., Liu, X., He, Y., Lyu, C., & Lu, J. (2025) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2025.1574145 · Cited by 1
Yimiletey, J., Li, Z., Wan, C., Velleman, S. G., & Yu, H. M. (2025) · Poultry Science · doi:10.1016/j.psj.2025.105735 · Cited by 1
Jacobsen, N. L., Nguyen, M., Morton, A. B., Cornelison, D., & Segal, S. S. (2025) · Microcirculation · doi:10.1111/micc.70024 · Cited by 1
Wang, D., Shan, D., Zhao, D., Dai, T., Liu, F., & Yan, C. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-07173-z · Cited by 1
Liao, Y., Fu, C., & Xing, S. (2025) · Scientific Reports · doi:10.1038/s41598-025-17688-6 · Cited by 1
Tan, Z., Pokhrel, B., & Jiang, H. (2025) · Cells · doi:10.3390/cells14221807 · Cited by 1
TBC1D1 functions as a negative regulator of satellite cells for muscle regeneration
Yang, X., Cao, Y., Mu, Y., Zhou, Y., Zhang, L., Ai, H., Zhu, D., Chen, S., & Wang, H. Y. (2025) · Nature Communications · doi:10.1038/s41467-025-65141-z · Cited by 1
European bilberry extract improved dietary advanced glycation end products-induced muscle damage
Liao, Y., Lin, S., Yang, N., Zhou, H., Mo, X., Wen, L., Liang, X., King, L., Zhou, S., Sun, Y., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157672 · Cited by 1
Zhang, L., Ye, X., Sun, S., Zhang, L., Gu, Y., Cao, S., Zhou, M., Sun, W., Fu, C., Zhang, Q., et al. (2025) · Veterinary Sciences · doi:10.3390/vetsci12121197 · Cited by 1
Thi, T. T. H., Griffin, K. H., Aragon, H., & Leach, J. K. (2025) · ACS Applied Bio Materials · doi:10.1021/acsabm.5c01833 · Cited by 1
Impact of exercise-induced DNA damage repair on age-related muscle weakness and sarcopenia
朱, 玲., Su, Y., & Su, Z. (2026) · Frontiers in Genetics · doi:10.3389/fgene.2025.1639224 · Cited by 2
Chen, Y., Gong, Y., Xu, X., Song, M., Sun, X., Luo, J., Guo, J., Li, L., & Zhang, H. (2026) · Cells · doi:10.3390/cells15020206 · Cited by 2
The role of dietary fat intake in muscle decline: a new perspective based on comprehensive evidence
Wu, T., Xia, J., Feng, Z., Wang, Y., Wang, J. P., Liao, W., & Sun, G. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108400 · Cited by 1
Zhiping, M., Liu, X., Liu, Y., Ma, H., & Yan, C. (2026) · Biology of Sex Differences · doi:10.1186/s13293-026-00851-7 · Cited by 1
Profiling the epigenomic landscape of late embryonic and adult mouse hind limb muscles
Queeno, S. R., Okamoto, A. S., Callahan, D. M., O’Neill, M. C., Capellini, T. D., & Sterner, K. N. (2026) · Scientific Reports · doi:10.1038/s41598-025-32705-4 · Cited by 1
A review of environmental, technological, and socio-economic aspects of cultured meat
Singh, R., Prasad, S., Younis, K., & Yousuf, O. (2026) · Discover Biotechnology · doi:10.1007/s44340-026-00052-3 · Cited by 2
Role and mechanism of SUCNR1 <?A3B2 pi129?>in muscle pathophysiology
Yan, X., Yang, Y., Zi-Qiang, D. U. A. N., Gen-Meng, W. A. N., Bao-Kai, T. I. A. N., Jiao, L. I. U., Chang, B., & Xue-Jie, Y. I. (2026) · Shengming kexue · doi:10.3724/cbls.2026013 · Cited by 1
Ekumi, K. M., Johnston, M. J., Murphy, M. P., Rakoczy, S. G., Painter, T., & Brown‐Borg, H. M. (2026) · NAR Molecular Medicine · doi:10.1093/narmme/ugag018 · 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
Wu, L., Zhang, Y., Zhang, G., Feng, X., Zhu, W., Yang, H., Ji, X., Yin, M., Li, S., Li, Y., et al. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-08087-0 · Cited by 1
Senescence dynamics define therapeutic windows for Duchenne muscular dystrophy in DBA/2-mdx mice
Calls, A., Tàrrega, A. B., Cisneros, A., Rommelfanger, M., Campanario, S., Grima-Terrén, M., Ramírez‐Pardo, I., Moiseeva, V., Lukesova, V., Andrés, E., et al. (2026) · Skeletal Muscle · doi:10.1186/s13395-026-00426-5 · Cited by 1
Self-citationMacrophage regulation of extracellular matrix remodeling in aging skeletal muscle
Cui, C., Nazario, J. C., Stephen, I. A., Baranzini, M., Zhang, Y., De, S., Sen, P., Ferrucci, L., & Gorospe, M. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103208 · Cited by 1
Single-cell resolution of skeletal muscle aging: Current paradigms and perspectives
Wang, Y., Yang, Y., Guan, W., Yu, W., Li, N., & Wang, D. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103272 · Cited by 1
An, J., Lai, G., Zuo, J., Yuan, J., Fu, L., Zhang, B., Zhang, X., Lv, Y., Guo, P., Qin, D., et al. (2026) · FEBS Journal · doi:10.1111/febs.70659 · Cited by 1
Chen, D., Gan, M., Lei, Y., Wang, X., Zan, J., Ye, Q., Zhou, X., Chen, L., Wang, Y., Zhao, Y., et al. (2026) · Molecules · doi:10.3390/molecules31162797 · Cited by 1
Preserved satellite cell pool in a laminin-α2-deficient model of congenital muscular dystrophy
Coelho, L. A., Ribeiro, A. F., Nogueira, L., de Vasconcelos, F. T. G. R., Bezerra, J. C., & Vainzof, M. (2026) · Disease Models & Mechanisms · doi:10.1242/dmm.052782 · Cited by 1
Franchi-Mendes, T., Silva, M., Cartaxo, A. L., Fernandes‐Platzgummer, A., Cabral, J. M. S., & da Silva, C. L. (2023) · Bioengineering · doi:10.3390/bioengineering10091067 · Cited by 1
Kametaka, S., Isobe, M., 古俣, 謙., MORINAGA, M., NAGAHATA, K., Lee, S., UCHIYAMA, Y., Shibata, M., & Sugiura, H. (2023) · Biomedical Research · doi:10.2220/biomedres.44.199 · Cited by 1
Qu, Z., Shi, L., Wu, Z., Lin, P., Zhang, G., Cong, X., Zhao, X., Ge, H., Yan, S., Jiang, L., et al. (2024) · The FASEB Journal · doi:10.1096/fj.202201065rr · Cited by 1
Inhibition of skeletal muscle differentiation by calciprotein particles in human primary myoblasts
Kohno, S., Eisuke, U. N. O., Goishi, K., Kharaghani, D., Uchibe, K., & Terayama, R. (2024) · Biomedical Research · doi:10.2220/biomedres.45.173 · Cited by 1
Regulation of intramuscular fat deposition by intestinal microbes in pigs
ZHENG, W., MengKuan, L. I. U., XinYu, L. V., Xiong, W. A. N. G., JinBao, B. A. I., Yin, J., & Ma, J. (2024) · Scientia Sinica Vitae · doi:10.1360/ssv-2024-0119 · Cited by 1
Wang, B. H., Yang, X., Li, C., Yang, R., Sun, T., & Yin, Y. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1373605 · Cited by 1
An aged-related structural study of DHPR tetrads in peripheral couplings of human skeletal muscle
Pietrangelo, L., Mancinelli, R., Fulle, S., & Boncompagni, S. (2024) · European Journal of Translational Myology · doi:10.4081/ejtm.2024.13273 · Cited by 1
Deletion of RBM20 exon 9 impairs skeletal muscle growth and satellite cell function in pigs
Zhang, L., Fu, C., Zhou, M., Miao, W., Sun, W., Xu, J., Cao, S., & Zhu, S. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.151076 · Cited by 1
He, J., Wan, Q., Du, L., Qin, Q., Zhao, L., & Dong, Q. (2025) · Neurogastroenterology & Motility · doi:10.1111/nmo.70138 · Cited by 1
Nuclear entry of AS160 as a transcriptional regulator of satellite cells for muscle regeneration
Yang, X., Cao, Y., Zhou, Y., Yao, Q., Rong, P., Wang, X., Chen, Q., Feng, W., Zhang, L., Ai, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64220-5 · Cited by 2
Ageing Skeletal Muscle: The Ubiquitous Muscle Stem Cell
Stewart, C. E. (2023) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-21410-3_14 · Cited by 1
Perdiguero, E., García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00138-3 · Cited by 1
Self-citationThe Immune Landscape of Murine Skeletal Muscle Regeneration and AgingPreprint
Sousa, N. S., Bica, M., Brás, M. F., Antunes, I. B., Encarnação, I. A., Costa, T., Martins, I. B., Barbosa‐Morais, N. L., Sousa‐Victor, P., & Neves, J. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4663954 · Cited by 1
Self-citationGong, Z., zhang, X., Cui, J., Chen, W., Huang, X., Yang, Q., Li, T., & Zhang, W. (2024) · Research Square · doi:10.21203/rs.3.rs-4300013/v1 · Cited by 1
Jacques, E., Garcia, P., Mercier, O., Hu, Y., Dégletagne, C., Ravent, J., Fall, S., Almeida, M. P., Wheeler, A. R., Angers, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.22.604619 · Cited by 1
Lovell, C. D., Sierra, I., Welter, E. M., Sandoval-Heglund, D., Li, N., Vanderbeck, A., Lengner, C. J., Lepper, C., & Anguera, M. C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.30.673230 · Cited by 1
Brown, A. D., Scaramozza, A., Zhang, H., Mahin, S., Suresh, N., Tsusaka, T., Eliazer, S., Liu, X., Feeley, B. T., & Brack, A. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.26.678822 · Cited by 1
Strzyz, P. J. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00443-w
Jia, Y., Wang, A., Wang, C., Zhai, J., Zhao, B., Liao, T., Cao, N., Su, R., He, L., Li, Y., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1369361/v1
Recapitulating human skeletal muscle in vitro
Urciuolo, A., Easler, M., & Elvassore, N. (2022) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2021.10.003
Buffalo long non-coding RNA gene11007 promotes myoblasts proliferation
Zhang, N., Xu, G., Sun, P., Wang, S., Zhu, Y., Duan, S., Jiang, M., Li, H., Wei, X., & Ma, Y. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.857044
From Barbells to Brawns: The Physiology of Resistance Exercise and Skeletal Muscle Growth
Park, J., Mcllvain, V., Rosenberg, J., Donovan, L., Desai, P., & Kim, J. Y. (2022) · The Korean Journal of Sports Medicine · doi:10.5763/kjsm.2022.40.3.151
Dey, P., Rajalaxmi, S., Thakur, P. S., Hashmi, M. A., Lal, H., Saini, N., Muralidharan, S., Math, R. G. H., Saha, P., Pundlik, S. S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.05.539524
Compromiso miogénico de las células satélites en las distrofias musculares
Vélez-Caballero, S. H., Cano-Martínez, L. J., & Coral‐Vázquez, R. M. (2023) · Investigación en Discapacidad · doi:10.35366/113830
Duran, P., Yang, B. A., Plaster, E. M., Eiken, M. K., Loebel, C., & Aguilar, C. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.20.576326
Immune privileges as a result of mutual regulation of the immune and stem systems
Karpenko, D. V. (2023) · Biochemistry (Moscow) · doi:10.31857/s0320972523110131
Hepatic stellate cells and their role in the formation of the progenitor cell niche
Жданов, В. В., Chaikovskii, A. V., & Pan, E. S. (2024) · Bulletin of Siberian Medicine · doi:10.20538/1682-0363-2024-1-126-133
Bizieff, A., Cheng, M., Chang, K., Mohammed, H., Ziari, N., Nyangau, E., Fitch, M. D., & Hellerstein, M. K. (2024) · The Journal of Physiology · doi:10.1113/jp286307
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
Wang, H., Guo, M., Lu, J.-Q., Chen, L.-Y., Liang, F., Huang, P., & Song, K.-Y. (2024) · Current Stem Cell Research & Therapy · doi:10.2174/011574888x360503241214045130
Elkordy, E. A. (2025) · Journal of Microscopy and Ultrastructure · doi:10.4103/jmau.jmau_133_24 · Cited by 1
Kolonay, D., Grueter, C. E., & Baskin, K. K. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5158818
Laksono, B. M., Bergsma, A. J., Iuliano, A., Veldhoen, D. Y., van Nieuwkoop, S., Boter, M., Leijten, L. M. E., Bauer, L., Munnink, B. B. O., Pijnappel, W. W. M. P., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.07.647509
Azad, T. D., Li, M., Chiu, P.-Y., Jones, K. E., Lord, E. L., Molina, C. A., Walker, C. T., Osorio, J. A., Pizones, J., Theologis, A. A., et al. (2025) · Spine Deformity · doi:10.1007/s43390-025-01124-w · Cited by 1
Kang, J., Zeng, Y., Li, N., He, L., Wang, H., Sun, K., & Zhao, Y. F. (2025) · STAR Protocols · doi:10.1016/j.xpro.2025.103962
Gong, W., Ding, W., Bou, T., Shi, L., Lin, Y., Shi, X., Li, Z., Wu, H.-R., Dugarjaviin, M., & Bai, D. (2025) · Frontiers in Genetics · doi:10.3389/fgene.2025.1630614
Kaura, V., Chang, L., Hopkins, P. M., & Shaw, M. (2025) · British Journal of Anaesthesia · doi:10.1016/j.bja.2025.05.060
Endothelial Piezo1 regulates muscle AKT abundance and mechanically induced muscle hypertrophyPreprint
Bartoli, F., Tickle, P. G., Gallagher, H., Debant, M., Cheng, C. W., Futers, T. S., Daou, H. N., Yuldasheva, N. Y., Beech, D. J., & Bowen, T. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.02.673617
Tumors mimic the niche to inhibit neighboring stem cell differentiation
Zhang, Y., Wang, Y., Song, J. H., Yan, L., Wang, Z., Song, D., Wang, H., Yang, S., Niu, L., Sun, C., et al. (2026) · eLife · doi:10.7554/elife.108910.4
Li, Y., Li, K., He, M., Liang, C., Wang, X., Qi, S., Zhang, R., Jiang, M., Zheng, Z., Wei, Z., et al. (2025) · PhotoniX · doi:10.1186/s43074-025-00191-6 · Cited by 1
Tumors mimic the niche to inhibit neighboring stem cell differentiationPreprint
Zhang, Y., Wang, Y., Song, J. H., Yan, L., Wang, Z., Song, D., Zhao, Y., & Zhao, S. (2025) · eLife · doi:10.7554/elife.108910.1
Tumors mimic the niche to inhibit neighboring stem cell differentiationPreprint
Zhang, Y., Wang, Y., Song, J. H., Yan, L., Wang, Z., Song, D., Wang, H., Yang, S., Niu, L., Sun, C., et al. (2025) · eLife · doi:10.7554/elife.108910
Zhang, Z., & Yang, X. (2025) · Archives of Medical Science · doi:10.5114/aoms/214480
A dedicated recycling bin keeps muscle healthy
Sartorelli, V. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01418-3
Southerland, K. W., Xu, Y., Peters, D. T., Lin, X., Wei, X., Xiang, Y., Fei, K., Olivere, L. A., Morowitz, J. M., Otto, J. C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26638317
Florczyk, U., Polak, K., Jelínková, Š., Bronisz-Budzyńska, I., Sabo, R., Bolisetty, S., Agarwal, A., Werner, E., Józkowicz, A., Stępniewski, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26027579
Southerland, K. W., Xu, Y., Peters, D., Lin, X., Wei, X., Xiang, Y., Fei, K., Olivere, L. A., Morowitz, J. M., Otto, J. C., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24546901
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