The ins and outs of muscle stem cell aging
Open accessAbstract
Skeletal muscle has a remarkable capacity to regenerate by virtue of its resident stem cells (satellite cells). This capacity declines with aging, although whether this is due to extrinsic changes in the environment and/or to cell-intrinsic mechanisms associated to aging has been a matter of intense debate. Furthermore, while some groups support that satellite cell aging is reversible by a youthful environment, others support cell-autonomous irreversible changes, even in the presence of youthful factors. Indeed, whereas the parabiosis paradigm has unveiled the environment as responsible for the satellite cell functional decline, satellite cell transplantation studies support cell-intrinsic deficits with aging. In this review, we try to shed light on the potential causes underlying these discrepancies. We propose that the experimental paradigm used to interrogate intrinsic and extrinsic regulation of stem cell function may be a part of the problem. The assays deployed are not equivalent and may overburden specific cellular regulatory processes and thus probe different aspects of satellite cell properties. Finally, distinct subsets of satellite cells may be under different modes of molecular control and mobilized preferentially in one paradigm than in the other. A better understanding of how satellite cells molecularly adapt during aging and their context-dependent deployment during injury and transplantation will lead to the development of efficacious compensating strategies that maintain stem cell fitness and tissue homeostasis throughout life.
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The regenerative capacity of SCs is influenced by both intrinsic modulators and the extrinsic microenvironment.
“The regenerative capacity of SCs is influenced by both intrinsic modulators and the extrinsic microenvironment13–15.”
From In vivo partial reprogramming of myofibers promotes muscle regeneration by remodeling the stem cell niche (2021) · cites this paper as [15]
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Inflamm‐aging: An Evolutionary Perspective on Immunosenescence
FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358 · see citing works
A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells1
Till, J. E., & McCulloch, E. A. (2010) · Radiation Research · doi:10.1667/rrxx28.1 · Cited by 4,036 · see citing works
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 · see citing works
A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells
Till, J. E., & McCulloch, E. A. (1961) · Radiation Research · doi:10.2307/3570892 · Cited by 3,770 · see citing works
Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders
Baker, D. J., Wijshake, T., Tchkonia, T., LeBrasseur, N. K., Childs, B. G., van de Sluis, B., Kirkland, J. L., & van Deursen, J. M. (2011) · Nature · doi:10.1038/nature10600 · Cited by 3,670 · see citing works
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 · see citing works
Asymmetric self-renewal and commitment of satellite stem cells in muscle
Kuang, S., Kuroda, K., Le Grand, F., & Rudnicki, M. A. (2007) · Cell · doi:10.1016/j.cell.2007.03.044 · Cited by 1,449 · cited 1× · see citing works
“The adult satellite cell pool is functionally heterogeneous, with subsets enriched for stem cell potential under transplantation conditions [13, 44, 45, 64].”
Molecular regulation of stem cell quiescence
Cheung, T. H., & Rando, T. A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3591 · Cited by 1,148 · cited 1× · see citing works
“They transit between quiescence and activation stages, their chromatin adopts bivalent states to facilitate rapid differentiation of selfrenewal, they are capable of undergoing symmetric and asymmetric divisions, their metabolism is specialized to adapt to their particular needs, and they are located within microenvir…”
Notch-Mediated Restoration of Regenerative Potential to Aged Muscle
Conboy, I. M., Conboy, M. J., Smythe, G. M., & Rando, T. A. (2003) · Science · doi:10.1126/science.1087573 · Cited by 1,121 · see citing works
Lepper, C., Partridge, T. A., & Fan, C.-M. (2011) · Development · doi:10.1242/dev.067595 · Cited by 1,105 · see citing works
Geriatric muscle stem cells switch reversible quiescence into senescence
Sousa-Victor, P., Gutarra, S., García-Prat, L., Rodriguez-Ubreva, J., Ortet, L., Ruiz-Bonilla, V., Jardí, M., Ballestar, E., González, S., Serrano, A. L., et al. (2014) · Nature · doi:10.1038/nature13013 · Cited by 1,010 · see citing works
Self-citationPax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration
Sambasivan, R., Yao, R., Kissenpfennig, A., Van Wittenberghe, L., Paldi, A., Gayraud-Morel, B., Guenou, H., Malissen, B., Tajbakhsh, S., & Galy, A. (2011) · Development · doi:10.1242/dev.067587 · Cited by 939 · see citing works
The aged niche disrupts muscle stem cell quiescence
Chakkalakal, J. V., Jones, K. M., Basson, M. A., & Brack, A. S. (2012) · Nature · doi:10.1038/nature11438 · Cited by 851 · see citing works
Self-citationRestoring systemic GDF11 levels reverses age-related dysfunction in mouse skeletal muscle
Sinha, M., Jang, Y. C., Oh, J., Khong, D., Wu, E. Y., Manohar, R., Miller, C., Regalado, S. G., Loffredo, F. S., Pancoast, J. R., et al. (2014) · Science · doi:10.1126/science.1251152 · Cited by 824 · see citing works
Clonal dynamics of native haematopoiesis
Sun, J., Ramos, A., Chapman, B., Johnnidis, J. B., Le, L., Ho, Y.-J., Klein, A. M., Hofmann, O., & Camargo, F. D. (2014) · Nature · doi:10.1038/nature13824 · Cited by 803 · see citing works
Stem cell aging: mechanisms, regulators and therapeutic opportunities
Oh, J., Lee, Y. D., & Wagers, A. J. (2014) · Nature Medicine · doi:10.1038/nm.3651 · Cited by 796 · see citing works
Lemos, D. R., Babaeijandaghi, F., Low, M., Chang, C.-K., Lee, S. T., Fiore, D., Zhang, R.-H., Natarajan, A., Nedospasov, S. A., & Rossi, F. M. V. (2015) · Nature Medicine · doi:10.1038/nm.3869 · Cited by 740 · see citing works
Ras Proteins Induce Senescence by Altering the Intracellular Levels of Reactive Oxygen Species
Lee, A. C., Fenster, B. E., Ito, H., Takeda, K., Bae, N. S., Hirai, T., Yu, Z.-X., Ferrans, V. J., Howard, B. H., & Finkel, T. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.12.7936 · Cited by 691 · see citing works
Rejuvenation of the muscle stem cell population restores strength to injured aged muscles
Cosgrove, B. D., Gilbert, P. M., Porpiglia, E., Mourkioti, F., Lee, S. P., Corbel, S. Y., Llewellyn, M. E., Delp, S. L., & Blau, H. M. (2014) · Nature Medicine · doi:10.1038/nm.3464 · Cited by 677 · see citing works
Pax7 is critical for the normal function of satellite cells in adult skeletal muscle
von Maltzahn, J., Jones, A. E., Parks, R. J., & Rudnicki, M. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307680110 · Cited by 602 · see citing works
Bernet, J. D., Doles, J. D., Hall, J. K., Kelly Tanaka, K., Carter, T. A., & Olwin, B. B. (2014) · Nature Medicine · doi:10.1038/nm.3465 · Cited by 573 · see citing works
Chromatin modifications as determinants of muscle stem cell quiescence and chronological aging
Liu, L., Cheung, T. H., Charville, G. W., Hurgo, B. M. C., Leavitt, T., Shih, J., Brunet, A., & Rando, T. A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.05.043 · Cited by 544 · see citing works
GDF11 increases with age and inhibits skeletal muscle regeneration
Egerman, M. A., Cadena, S. M., Gilbert, J. A., Meyer, A., Nelson, H. N., Swalley, S. E., Mallozzi, C., Jacobi, C., Jennings, L. L., Clay, I., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.010 · Cited by 527 · see citing works
Self-citationInflammaging: disturbed interplay between autophagy and inflammasomes
Salminen, A., Kaarniranta, K., & Kauppinen, A. (2012) · Aging · doi:10.18632/aging.100444 · Cited by 511 · see citing works
Rocheteau, P., Gayraud-Morel, B., Siegl-Cachedenier, I., Blasco, M. A., & Tajbakhsh, S. (2012) · Cell · doi:10.1016/j.cell.2011.11.049 · Cited by 510 · see citing works
Imbalance between pSmad3 and Notch induces CDK inhibitors in old muscle stem cells
Carlson, M. E., Hsu, M., & Conboy, I. M. (2008) · Nature · doi:10.1038/nature07034 · Cited by 483 · see citing works
Endocytosis of Receptor Tyrosine KinasesPreprint
Goh, L. K., & Sorkin, A. D. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a017459 · Cited by 462 · see citing works
Inhibition of JAK-STAT signaling stimulates adult satellite cell function
Price, F. D., von Maltzahn, J., Bentzinger, C. F., Dumont, N. A., Yin, H., Chang, N. C., Wilson, D. H., Frenette, J., & Rudnicki, M. A. (2014) · Nature Medicine · doi:10.1038/nm.3655 · Cited by 433 · see citing works
Fry, C. S., Lee, J. D., Mula, J., Kirby, T. J., Jackson, J. R., Liu, F., Yang, L., Mendias, C. L., Dupont-Versteegden, E. E., McCarthy, J. J., et al. (2015) · Nature Medicine · doi:10.1038/nm.3710 · Cited by 432 · see citing works
The regeneration of skeletal muscle fibers following injury
Carlson, B. M., & Faulkner, J. A. (1983) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-198315030-00003 · Cited by 420 · see citing works
Muscle transplantation between young and old rats: age of host determines recovery
Carlson, B. M., & Faulkner, J. A. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.256.6.c1262 · Cited by 417 · see citing works
Elabd, C., Cousin, W., Upadhyayula, P., Chen, R. Y., Chooljian, M. S., Li, J., Kung, S., Jiang, K. P., & Conboy, I. M. (2014) · Nature Communications · doi:10.1038/ncomms5082 · Cited by 411 · see citing works
Tissue-specific stem cells: Lessons from the skeletal muscle satellite cell
Brack, A. S., & Rando, T. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.04.001 · Cited by 409 · see citing works
Self-citationSTAT3 signaling controls satellite cell expansion and skeletal muscle repair
Tierney, M. T., Aydogdu, T., Sala, D., Malecova, B., Gatto, S., Puri, P. L., Latella, L., & Sacco, A. (2014) · Nature Medicine · doi:10.1038/nm.3656 · Cited by 401 · see citing works
Short-Term Calorie Restriction Enhances Skeletal Muscle Stem Cell Function
Cerletti, M., Jang, Y. C., Finley, L. W. S., Haigis, M. C., & Wagers, A. J. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.04.002 · Cited by 397 · see citing works
Shea, K. L., Xiang, W., LaPorta, V. S., Licht, J. D., Keller, C., Basson, M. A., & Brack, A. S. (2010) · Cell stem cell · doi:10.1016/j.stem.2009.12.015 · Cited by 351 · see citing works
Self-citationMcCulloch, E. A., & Till, J. E. (1960) · Radiation Research · doi:10.2307/3570877 · Cited by 336 · see citing works
A Population of Myogenic Stem Cells That Survives Skeletal Muscle Aging
Collins, C. A., Zammit, P. S., Ruiz, A. P., Morgan, J. E., & Partridge, T. A. (2007) · Stem Cells · doi:10.1634/stemcells.2006-0372 · Cited by 320 · see citing works
Complement C1q Activates Canonical Wnt Signaling and Promotes Aging-Related Phenotypes
Naito, A. T., Sumida, T., Nomura, S., Liu, M.-L., Higo, T., Nakagawa, A., Okada, K., Sakai, T., Hashimoto, A., Hara, Y., et al. (2012) · Cell · doi:10.1016/j.cell.2012.03.047 · Cited by 320 · see citing works
Brack, A. S., Bildsoe, H., & Hughes, S. M. (2005) · Journal of Cell Science · doi:10.1242/jcs.02602 · Cited by 308 · see citing works
Self-citationConboy, M. J., Karasov, A. O., & Rando, T. A. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050102 · Cited by 287 · cited 1× · see citing works
“Over the past few years, it has become apparent that functional heterogeneity exists within the satellite cell pool [13, 44–46].”
Conboy, M. J., Conboy, I. M., & Rando, T. A. (2013) · Aging Cell · doi:10.1111/acel.12065 · Cited by 265 · see citing works
Age‐associated Changes in the Response of Skeletal Muscle Cells to Exercise and Regenerationa
Grounds, M. D. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09894.x · Cited by 264 · see citing works
Day, K., Shefer, G., Shearer, A., & Yablonka-Reuveni, Z. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.01.006 · Cited by 254 · see citing works
Understanding the Process of Fibrosis in Duchenne Muscular Dystrophy
Kharraz, Y., Guerra, J., Pessina, P., Serrano, A. L., & Muñoz‐Cánoves, P. (2014) · BioMed Research International · doi:10.1155/2014/965631 · Cited by 251 · see citing works
Self-citationIntrinsic Changes and Extrinsic Influences of Myogenic Stem Cell Function During Aging
Brack, A. S., & Rando, T. A. (2007) · Stem Cell Reviews · doi:10.1007/s12015-007-9000-2 · Cited by 238 · see citing works
Self-citationRamsey, M. R., & Sharpless, N. E. (2006) · Nature Cell Biology · doi:10.1038/ncb1106-1213 · Cited by 237 · see citing works
Juan, A. H., Derfoul, A., Feng, X., Ryall, J. G., Dell’Orso, S., Pasut, A., Zare, H., Simone, J. M., Rudnicki, M. A., & Sartorelli, V. (2011) · Genes & Development · doi:10.1101/gad.2027911 · Cited by 218 · see citing works
Reactive oxygen species and hematopoietic stem cell senescence
Shao, L., Li, H., Pazhanisamy, S. K., Meng, A., Wang, Y., & Zhou, D. (2011) · International Journal of Hematology · doi:10.1007/s12185-011-0872-1 · Cited by 198 · see citing works
Ex Vivo Expansion and In Vivo Self-Renewal of Human Muscle Stem Cells
Charville, G. W., Cheung, T. H., Yoo, B., Santos, P. J. F., Lee, G., Shrager, J. B., & Rando, T. A. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.08.004 · Cited by 196 · see citing works
DNA damage response in adult stem cells: pathways and consequences
Mandal, P. K., Blanpain, C., & Rossi, D. J. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3060 · Cited by 195 · see citing works
Muscle stem cell aging: regulation and rejuvenation
Sousa-Victor, P., García-Prat, L., Serrano, A. L., Perdiguero, E., & Muñoz-Cánoves, P. (2015) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2015.03.006 · Cited by 163 · see citing works
Self-citationFunctional dysregulation of stem cells during aging: a focus on skeletal muscle stem cells
García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2013) · The FEBS Journal · doi:10.1111/febs.12221 · Cited by 152 · see citing works
Self-citationChakkalakal, J. V., Christensen, J., Xiang, W., Tierney, M. T., Boscolo, F. S., Sacco, A., & Brack, A. S. (2014) · Development · doi:10.1242/dev.100842 · Cited by 148 · see citing works
Self-citationAge-dependent imbalance of the antioxidative system in human satellite cells
Fulle, S., Donna, S. D., Puglielli, C., Pietrangelo, T., Beccafico, S., Bellomo, R. G., Protasi, F., & Fanò, G. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.11.006 · Cited by 143 · see citing works
Delayed but excellent myogenic stem cell response of regenerating geriatric skeletal muscles in mice
Shavlakadze, T., McGeachie, J. K., & Grounds, M. D. (2009) · Biogerontology · doi:10.1007/s10522-009-9260-0 · Cited by 135 · see citing works
Shared signaling systems in myeloid cell-mediated muscle regeneration
Tidball, J. G., Dorshkind, K. A., & Wehling‐Henricks, M. (2014) · Development · doi:10.1242/dev.098285 · Cited by 134 · see citing works
Bigot, A., Duddy, W. J., Ouandaogo, Z. G., Négroni, E., Mariot, V., Ghimbovschi, S. D., Harmon, B. T., Wielgosik, A., Loiseau, C., Devaney, J., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.067 · Cited by 125 · see citing works
Prevention of Muscle Aging by Myofiber-Associated Satellite Cell Transplantation
Hall, J. K., Banks, G., Chamberlain, J., & Olwin, B. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3001081 · Cited by 124 · see citing works
Long-term erythropoietic repopulating ability of old, young, and fetal stem cells.
Harrison, D. E. (1983) · The Journal of Experimental Medicine · doi:10.1084/jem.157.5.1496 · Cited by 123 · see citing works
Yousef, H., Conboy, M. J., Morgenthaler, A., Schlesinger, C., Bugaj, L. J., Paliwal, P., Greer, C. D., Conboy, I. M., & Schaffer, D. V. (2015) · Oncotarget · doi:10.18632/oncotarget.3851 · Cited by 115 · see citing works
ROS ‐generating oxidases N ox1 and N ox4 contribute to oncogenic R as‐induced premature senescence
Kodama, R., Kato, M., Furuta, S., Ueno, S., Zhang, Y., Matsuno, K., Yabe‐Nishimura, C., Tanaka, E., & Kamata, T. (2012) · Genes to Cells · doi:10.1111/gtc.12015 · Cited by 107 · see citing works
Pietrangelo, T., Puglielli, C., Mancinelli, R., Beccafico, S., Fanò, G., & Fulle, S. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2009.05.002 · Cited by 98 · see citing works
Age dependent increase in the levels of osteopontin inhibits skeletal muscle regeneration
Paliwal, P., Pishesha, N., Wijaya, D., & Conboy, I. M. (2012) · Aging · doi:10.18632/aging.100477 · Cited by 89 · see citing works
CHARGÉ, S. B. P., Brack, A. S., & Hughes, S. M. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00206.2002 · Cited by 84 · see citing works
Self-citationNumb is required to prevent p53-dependent senescence following skeletal muscle injury
Le Roux, I., Konge, J., Le Cam, L., Flamant, P., & Tajbakhsh, S. (2015) · Nature Communications · doi:10.1038/ncomms9528 · Cited by 81 · see citing works
Ferdousi, L. V., Rocheteau, P., Chayot, R., Montagne, B., Chaker, Z., Flamant, P., Tajbakhsh, S., & Ricchetti, M. (2014) · Stem Cell Research · doi:10.1016/j.scr.2014.08.005 · Cited by 77 · see citing works
Geroconversion of aged muscle stem cells under regenerative pressure
Sousa-Victor, P., Perdiguero, E., & Muñoz-Cánoves, P. (2014) · Cell Cycle · doi:10.4161/15384101.2014.965072 · Cited by 68 · see citing works
Self-citationCellular Mechanisms of Somatic Stem Cell Aging
Jung, Y., & Brack, A. S. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00014-7 · Cited by 60 · see citing works
Self-citationAged skeletal muscle retains the ability to fully regenerate functional architecture
Lee, A. S. J., Anderson, J. E., Joya, J. E., Head, S. I., Pather, N., Kee, A. J., Gunning, P. W., & Hardeman, E. C. (2013) · BioArchitecture · doi:10.4161/bioa.24966 · Cited by 59 · see citing works
Smythe, G. M., Shavlakadze, T., Roberts, P., Davies, M. J., McGeachie, J. K., & Grounds, M. D. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.02.005 · Cited by 57 · see citing works
GDF11 and the Mythical Fountain of Youth
Brun, C. E., & Rudnicki, M. A. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.009 · Cited by 56 · see citing works
Gene expression profiling of human satellite cells during muscular aging using cDNA arrays
Bortoli, S., Renault, V. M., Eveno, E., Auffray, C., Butler-Browne, G. S., & Piétu, G. (2003) · Gene · doi:10.1016/j.gene.2003.08.025 · Cited by 53 · see citing works
Baj, A., Bettaccini, A. A., Casalone, R., Sala, A., Cherubino, P., & Toniolo, A. (2005) · Journal of Translational Medicine · doi:10.1186/1479-5876-3-21 · Cited by 41 · see citing works
Didier, N., Hourdé, C., Amthor, H., Marazzi, G., & Sassoon, D. A. (2012) · EMBO Molecular Medicine · doi:10.1002/emmm.201101075 · Cited by 40 · see citing works
Reanalysis of parabiosis of obesity mutants in the age of leptin
Zeng, W., Lu, Y.-H., Lee, J., & Friedman, J. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510378112 · Cited by 14 · see citing works
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Sarcopenia: Aging-Related Loss of Muscle Mass and Function
Larsson, L., Degens, H., Li, M., Salviati, L., Lee, Y. I., Thompson, W., Kirkland, J. L., & Sandri, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00061.2017 · Cited by 1,797 · see citing works
Skeletal muscle: A review of molecular structure and function, in health and disease
Mukund, K., & Subramaniam, S. (2019) · Wiley Interdisciplinary Reviews: Systems Biology and Medicine · doi:10.1002/wsbm.1462 · Cited by 601 · see citing works
Csapo, R., Gumpenberger, M., & Wessner, B. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00253 · Cited by 432 · see citing works
Lukjanenko, L., Karaz, S., Stuelsatz, P., Gurriaran-Rodriguez, U., Michaud, J., Dammone, G., Sizzano, F., Mashinchian, O., Ancel, S., Migliavacca, E., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2018.12.014 · Cited by 374 · see citing works
Stout, A. J., Mirliani, A. B., Rittenberg, M. L., Shub, M., White, E. C., Yuen, J. S. K., & Kaplan, D. L. (2022) · Communications Biology · doi:10.1038/s42003-022-03423-8 · Cited by 313 · see citing works
Effects of Aging on Fracture Healing
Clark, D. R., Nakamura, M. C., Miclau, T., & Marcucio, R. (2017) · Current Osteoporosis Reports · doi:10.1007/s11914-017-0413-9 · Cited by 293 · see citing works
Skeletal Muscle Wasting and Renewal: A Pivotal Role of Myokine IL-6
Belizário, J. E., Fontes-Oliveira, C. C., Borges, J. P., Kashiabara, J. A., & Vannier, E. (2016) · SpringerPlus · doi:10.1186/s40064-016-2197-2 · Cited by 244 · see citing works
Hernando-Herraez, I., Evano, B., Stubbs, T., Commere, P.-H., Jan Bonder, M., Clark, S., Andrews, S., Tajbakhsh, S., & Reik, W. (2019) · Nature Communications · doi:10.1038/s41467-019-12293-4 · Cited by 236 · see citing works
Bedi, A., Bishop, J. Y., Keener, J. D., Lansdown, D. A., Levy, O., MacDonald, P. B., Maffulli, N., Oh, J. H., Sabesan, V. J., Sánchez‐Sotelo, J., et al. (2024) · Nature Reviews Disease Primers · doi:10.1038/s41572-024-00492-3 · Cited by 212 · see citing works
Murine single-cell RNA-seq reveals cell-identity- and tissue-specific trajectories of aging
Kimmel, J. C., Penland, L., Rubinstein, N. D., Hendrickson, D. G., Kelley, D. R., & Rosenthal, A. Z. (2019) · Genome Research · doi:10.1101/gr.253880.119 · Cited by 184 · see citing works
Regulation of Muscle Stem Cell Functions: A Focus on the p38 MAPK Signaling Pathway
Segalés, J., Perdiguero, E., & Muñoz‐Cánoves, P. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00091 · Cited by 209 · see citing works
Self-citationAhmed, A. S. I., Sheng, M. H. ‐., Wasnik, S., Baylink, D. J., & Lau, K. ‐. W. (2017) · World Journal of Experimental Medicine · doi:10.5493/wjem.v7.i1.1 · Cited by 202 · see citing works
Sarcopenic 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 · see citing works
Wnt4 from the Niche Controls the Mechano-Properties and Quiescent State of Muscle Stem Cells
Eliazer, S., Muncie, J. M., Christensen, J., Sun, X., D’Urso, R. S., Weaver, V. M., & Brack, A. S. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.08.007 · Cited by 171 · see citing works
“In contexts of increased SC turnover such as in muscular dystrophy, aging, or in transgenic mice harboring cell cycle mutations, SC function is impaired (Brack and Munoz-Canoves, 2016; Brack and Rando, 2007; Chakkalakal et al., 2014) For many years, SC quiescence has been considered to be a reversible but homogenous s…”
BackgroundSelf-citationStem Cell Aging in Skeletal Muscle Regeneration and Disease
Yamakawa, H., Kusumoto, D., Hashimoto, H., & Yuasa, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051830 · Cited by 156 · see citing works
Regulatory T cells and skeletal muscle regeneration
Schiaffino, S., Pereira, M. G., Ciciliot, S., & Rovere-Querini, P. (2017) · The FEBS Journal · doi:10.1111/febs.13827 · Cited by 136 · see citing works
Subramanian, A., Kanzaki, L. F., Galloway, J. L., & Schilling, T. F. (2018) · eLife · doi:10.7554/elife.38069 · Cited by 140 · see citing works
Muscle wasting and aging: Experimental models, fatty infiltrations, and prevention
Brioche, T., Pagano, A. F., Py, G., & Chopard, A. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.04.006 · Cited by 129 · see citing works
Regenerative function of immune system: Modulation of muscle stem cells
Saini, J., McPhee, J. S., Al-Dabbagh, S., Stewart, C. E., & Al‐Shanti, N. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.03.006 · Cited by 129 · see citing works
Proteostatic and Metabolic Control of Stemness
García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.04.011 · Cited by 123 · see citing works
Self-citationJoanisse, S., Nederveen, J. P., Snijders, T., McKay, B. R., & Parise, G. (2016) · Gerontology · doi:10.1159/000450922 · Cited by 124 · see citing works
Pten is necessary for the quiescence and maintenance of adult muscle stem cells
Yue, F., Bi, P., Wang, C., Shan, T., Nie, Y., Ratliff, T. L., Gavin, T. P., & Kuang, S. (2017) · Nature Communications · doi:10.1038/ncomms14328 · Cited by 120 · see citing works
Wang, C., Rabadan Ros, R., Martinez-Redondo, P., Ma, Z., Shi, L., Xue, Y., Guillen-Guillen, I., Huang, L., Hishida, T., Liao, H.-K., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23353-z · Cited by 119 · see citing works
An epigenetic clock for human skeletal muscle
Voisin, S. A. C., Harvey, N. R., Haupt, L. M., Griffiths, L. R., Ashton, K. J., Coffey, V. G., Doering, T. M., Thompson, J. M., Benedict, C., Cedernaes, J., et al. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12556 · Cited by 111 · see citing works
Muñoz‐Cánoves, P., Neves, J., & Sousa‐Victor, P. (2019) · FEBS Journal · doi:10.1111/febs.15182 · Cited by 111 · see citing works
Self-citationThe Role of Innate and Adaptive Immune Cells in Skeletal Muscle Regeneration
Ziemkiewicz, N., Hilliard, G. M., Pullen, N. A., & Garg, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063265 · Cited by 100 · see citing works
Schüler, S. C., Kirkpatrick, J. M., Schmidt, M., Santinha, D., Koch, P., Di Sanzo, S., Cirri, E., Hemberg, M., Ori, A., & von Maltzahn, J. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109223 · Cited by 106 · see citing works
Loreti, M., & Sacco, A. (2022) · npj Regenerative Medicine · doi:10.1038/s41536-022-00204-z · Cited by 94 · see citing works
Exploring the Impact of Obesity on Skeletal Muscle Function in Older Age
Morgan, P. T., Smeuninx, B., & Breen, L. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.569904 · Cited by 99 · see citing works
Aging induces aberrant state transition kinetics in murine muscle stem cells
Kimmel, J. C., Hwang, A. B., Scaramozza, A., Marshall, W. F., & Brack, A. S. (2020) · Development · doi:10.1242/dev.183855 · Cited by 95 · see citing works
Self-citationDecoding the relationship between ageing and amyotrophic lateral sclerosis: a cellular perspective
Pandya, V. A., & Patani, R. (2019) · Brain · doi:10.1093/brain/awz360 · Cited by 85 · see citing works
Meta‐analysis of genome‐wide DNA methylation and integrative omics of age in human skeletal muscle
Voisin, S. A. C., Jacques, M., Landen, S., Harvey, N. R., Haupt, L. M., Griffiths, L. R., Gancheva, S., Ouni, M., Jähnert, M., Ashton, K. J., et al. (2021) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12741 · Cited by 84 · see citing works
Exercise promotes satellite cell contribution to myofibers in a load-dependent manner
Masschelein, E., D’Hulst, G., Zvick, J., Hinte, L. C., Soro-Arnáiz, I., Gorski, T., von Meyenn, F., Bar‐Nur, O., & Bock, K. D. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-00237-2 · Cited by 82 · see citing works
Obesity as a premature aging phenotype — implications for sarcopenic obesity
Nunan, E. L., Wright, C. L., Semola, O. A., Subramanian, M., Balasubramanian, P., Lovern, P. C., Fancher, I. S., & Butcher, J. T. (2022) · GeroScience · doi:10.1007/s11357-022-00567-7 · Cited by 83 · see citing works
Yue, F., Bi, P., Wang, C., Li, J., Liu, X., & Kuang, S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.11.002 · Cited by 81 · see citing works
Hwang, A. B., & Brack, A. S. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.008 · Cited by 80 · see citing works
Self-citationGarg, K., & Boppart, M. D. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00594.2016 · Cited by 77 · see citing works
Reidy, P., McKenzie, A. I., Mahmassani, Z., Petrocelli, J. J., Nelson, D. B., Lindsay, C. C., Gardner, J. E., Morrow, V. R., Keefe, A., Huffaker, T., et al. (2019) · American Journal of Physiology. Endocrinology and Metabolism · doi:10.1152/ajpendo.00422.2018 · Cited by 67 · see citing works
Multiomics reveals glutathione metabolism as a driver of bimodality during stem cell aging
Benjamin, D. I., Brett, J. O., Both, P., Benjamin, J. S., Ishak, H. D., Kang, J., Kim, S., Chung, M., Arjona, M., Nutter, C. W., et al. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.02.001 · Cited by 79 · see citing works
De Gasperi, R., Hamidi, S., Harlow, L. M., Ksiezak-Reding, H., Bauman, W. A., & Cardozo, C. P. (2017) · Scientific Reports · doi:10.1038/s41598-017-13105-9 · Cited by 75 · see citing works
Harper (2016) · doi:10.1161/circresaha.116.307962 · Cited by 74 · see citing works
Self-citationXiong, G., Hindi, S. M., Mann, A. K., Gallot, Y. S., Bohnert, K. R., Cavener, D. R., Whittemore, S. R., & Kumar, A. (2017) · eLife · doi:10.7554/elife.22871 · Cited by 74 · see citing works
Scalable 3D Printed Molds for Human Tissue Engineered Skeletal Muscle
Capel, A. J., Rimington, R. P., Fleming, J. W., Player, D. J., Baker, L. A., Turner, M. C., Jones, J. M., Martin, N. R. W., Ferguson, R. A., Mudera, V., et al. (2019) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2019.00020 · Cited by 75 · see citing works
Graça, F. A., Stephan, A., Minden‐Birkenmaier, B. A., Shirinifard, A., Wang, Y., Demontis, F., & Labelle, M. (2023) · Nature Communications · doi:10.1038/s41467-023-38624-0 · Cited by 73 · see citing works
Muscular Atrophy and Sarcopenia in the Elderly: Is There a Role for Creatine Supplementation?
Dolan, E., Artioli, G. G., Pereira, R. M. R., & Gualano, B. (2019) · Biomolecules · doi:10.3390/biom9110642 · Cited by 72 · see citing works
Schätzl, T., Kaiser, L., & Deigner, H. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01760-1 · Cited by 69 · see citing works
Zullo, A., Fleckenstein, J., Schleip, R., Hoppe, K., Wearing, S. C., & Klingler, W. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00592 · Cited by 70 · see citing works
Influence of physical exercise on microRNAs in skeletal muscle regeneration, aging and diseases
Ultimo, S., Zauli, G., Martelli, A. M., Vitale, M., McCubrey, J. A., Capitani, S., & Neri, L. M. (2018) · Oncotarget · doi:10.18632/oncotarget.24991 · Cited by 62 · see citing works
Facioscapulohumeral Muscular Dystrophy
DeSimone, A. M., Pakuła, A., Lek, A., & Emerson, C. P. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160039 · Cited by 62 · see citing works
Ageing of skeletal muscle extracellular matrix and mitochondria: finding a potential link
Cai, L., Shi, L., Peng, Z., Sun, Y., & Chen, J. (2023) · Annals of Medicine · doi:10.1080/07853890.2023.2240707 · Cited by 60 · see citing works
Sarcopenic Obesity and Cardiovascular Disease: An Overlooked but High-Risk Syndrome
Mirzai, S., Carbone, S., Batsis, J. A., Kritchevsky, S. B., Kitzman, D. W., & Shapiro, M. D. (2024) · Current Obesity Reports · doi:10.1007/s13679-024-00571-2 · Cited by 65 · see citing works
Stem Cell Aging in Lifespan and Disease: A State-of-the-Art Review
Sameri, S., Samadi, P., Dehghan, R., Salem, E., Hosseini, N. F., & Amini, R. (2020) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x15666200213105155 · Cited by 55 · see citing works
Ebrahimi, M., Lad, H., Fusto, A., Tiper, Y., Datye, A., Nguyen, C. T., Jacques, E., Moyle, L. A., Nguyen, T. M., Musgrave, B., et al. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.05.020 · Cited by 55 · see citing works
Serum Response Factor in muscle tissues: from development to ageing
Coletti, D., Daou, N., Hassani, M., Li, Z., & Parlakian, A. (2016) · European Journal of Translational Myology · doi:10.4081/ejtm.2016.6008 · Cited by 53 · see citing works
The biphasic and age-dependent impact of klotho on hallmarks of aging and skeletal muscle function
Clemens, Z. J., Sivakumar, S., Pius, A., Sahu, A., Shinde, S. S., Mamiya, H., Luketich, N., Cui, J., Dixit, P. D., Hoeck, J. D., et al. (2021) · eLife · doi:10.7554/elife.61138 · Cited by 51 · see citing works
Sphingolipids accumulate in aged muscle, and their reduction counteracts sarcopenia
Laurila, P., Wohlwend, M., de Lima, T. I., Luan, P., Herzig, S., Zanou, N., Crisol, B., Sleiman, M. S. B., Porcu, E., Gallart‐Ayala, H., et al. (2022) · Nature Aging · doi:10.1038/s43587-022-00309-6 · Cited by 53 · see citing works
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 46 · see citing works
Skeletal muscle as an experimental model of choice to study tissue aging and rejuvenation
Etienne, J., Liu, C., Skinner, C. M., Conboy, M. J., & Conboy, I. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-0222-1 · Cited by 43 · see citing works
McKenna, C. F., & Fry, C. S. (2017) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000409 · Cited by 45 · see citing works
MicroRNA regulatory networks in the pathogenesis of sarcopenia
Yin, J., Qian, Z., Chen, Y., Li, Y., & Zhou, X. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15197 · Cited by 45 · see citing works
Liu, Y., Wang, Q., Zhang, Z., Fu, R., Zhou, T., Long, C., He, T., Yang, D., Li, Z., & Peng, S. (2021) · Bone · doi:10.1016/j.bone.2021.115886 · Cited by 44 · see citing works
The Effects of Muscle Cell Aging on Myogenesis
Moustogiannis, A., Philippou, Α., Taso, O. S., Zevolis, E., Pappa, M. B., Chatzigeorgiou, A., & Koutsilieris, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073721 · Cited by 44 · see citing works
Transcriptome and epigenome diversity and plasticity of muscle stem cells following transplantation
Evano, B., Gill, D., Hernando-Herraez, I., Comai, G., Stubbs, T. M., Commere, P.-H., Reik, W., & Tajbakhsh, S. (2020) · PLOS Genetics · doi:10.1371/journal.pgen.1009022 · Cited by 40 · see citing works
Rufenach, B., & Petegem, F. V. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100874 · Cited by 40 · see citing works
LncRNAs regulating stemness in aging
Sousa‐Franco, A., Rebelo, K., da Rocha, S. T., & de Jesus, B. B. (2018) · Aging Cell · doi:10.1111/acel.12870 · Cited by 38 · see citing works
Muscle stem cell renewal suppressed by GAS1 can be reversed by GDNF in mice
Li, L., Rozo, M., Yue, S., Zheng, X., Tan, F. J., Lepper, C., & Fan, C. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0110-3 · Cited by 40 · see citing works
Olthoff, J. T., Lindsay, A., Abo‐Zahrah, R., Baltgalvis, K. A., Patrinostro, X., Belanto, J. J., Yu, D., Perrin, B. J., Garry, D. J., Rodney, G. G., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07639-3 · Cited by 38 · see citing works
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 · see citing works
Delineating the relationship between immune system aging and myogenesis in muscle repair
Tobin, S. W., Alibhai, F. J., Wlodarek, L., Yeganeh, A., Millar, S., Wu, J., Li, S., Weisel, R. D., & Li, R. (2021) · Aging Cell · doi:10.1111/acel.13312 · Cited by 36 · see citing works
Fracture repair in the elderly: Clinical and experimental considerations
Meinberg, E., Clark, D. R., Miclau, K. R., Marcucio, R., & Miclau, T. (2019) · Injury · doi:10.1016/j.injury.2019.05.005 · Cited by 36 · see citing works
Aging, metabolism and stem cells: Spotlight on muscle stem cells
García-Prat, L., & Muñoz-Cánoves, P. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.08.021 · Cited by 34 · see citing works
Self-citationThe Role of p53 in Determining Mitochondrial Adaptations to Endurance Training in Skeletal Muscle
Beyfuss, K. A., Erlich, A. T., Triolo, M., & Hood, D. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-32887-0 · Cited by 34 · see citing works
Giza, S., Mojica-Santiago, J., Parafati, M., Malany, L. K., Platt, D., Schmidt, C. E., Coen, P. M., & Malany, S. (2022) · Aging Cell · doi:10.1111/acel.13650 · Cited by 32 · see citing works
Restoration of CPEB4 prevents muscle stem cell senescence during aging
Zeng, W., Zhang, W., Tse, E. H. Y., Liu, J., Dong, A., Lam, K. S. W., Luan, S., Küng, W., Chan, T. C., & Cheung, T. H. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.05.012 · Cited by 34 · see citing works
Effect of source animal age upon macrophage response to extracellular matrix biomaterials
LoPresti, S. T., & Brown, B. N. (2018) · Journal of Immunology and Regenerative Medicine · doi:10.1016/j.regen.2018.03.004 · Cited by 33 · see citing works
Dong, W.-X., Chen, W., Zou, H., Shen, Z.-L., Yu, D., Chen, W., Jiang, H., Yan, X., & Yu, Z. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/9159101 · Cited by 31 · see citing works
Skeletal muscle aging – Stem cells in the spotlight
Henze, H., Jung, M. J., Ahrens, H. E., Steiner, S., & von Maltzahn, J. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111283 · Cited by 28 · see citing works
Robinson, D. C. L., Ritso, M., Nelson, G. M., Mokhtari, Z., Nakka, K. K., Bandukwala, H., Goldman, S. R., Park, P. J., Mounier, R., Chazaud, B., et al. (2020) · Developmental Cell · doi:10.1016/j.devcel.2021.02.025 · Cited by 29 · see citing works
Moraes, M. N., Mezzalira, N., de Assis, L. V. M., Menaker, M., Güler, A. D., & Castrucci, A. M. D. L. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.11.010 · Cited by 28 · see citing works
Circadian Clock-Controlled Checkpoints in the Pathogenesis of Complex Disease
Li, M., Xin, H., Yuan, Y., Yang, X., Li, H., Tian, D., Zhang, H., Zhang, Z., Han, T.-L., Chen, Q., et al. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.721231 · Cited by 29 · see citing works
Epigenetic erosion of H4K20me1 induced by inflammation drives aged stem cell ferroptosis
Blanc, R. S., Shah, N., Hachmer, S., Salama, N., Meng, F. W., Mousaei, A., Puri, G., Hwang, J. H., Wacker, E. E., Yang, B. A., et al. (2025) · Nature Aging · doi:10.1038/s43587-025-00902-5 · Cited by 31 · see citing works
Goichberg, P. (2016) · Stem Cell Reviews and Reports · doi:10.1007/s12015-016-9663-7 · Cited by 26 · see citing works
Hippo pathway effectors YAP and TAZ and their association with skeletal muscle ageing
Setiawan, I., Sanjaya, A., Lesmana, R., Yen, P. M., & Goenawan, H. (2021) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-021-00787-z · Cited by 24 · see citing works
Tokarz, J., Möller, G., Artati, A., Huber, S., Zeigerer, A., Blaauw, B., Adamski, J., & Dyar, K. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22157958 · Cited by 23 · see citing works
Roy, A., da Silva, M. T., Bhat, R., Bohnert, K. R., Iwawaki, T., & Kumar, A. (2021) · eLife · doi:10.7554/elife.73215 · Cited by 22 · see citing works
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 21 · see citing works
Reduced growth rate of aged muscle stem cells is associated with impaired mechanosensitivity
Haroon, M. F., Boers, H. E., Bakker, A. D., Bloks, N. G. C., Hoogaars, W. M. H., Giordani, L., Musters, R. J. P., Deldicque, L., Koppo, K., Grand, F. L., et al. (2022) · Aging · doi:10.18632/aging.203830 · Cited by 21 · see citing works
Stocks, B., Dent, J. R., Joanisse, S., McCurdy, C. E., & Philp, A. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00941 · Cited by 21 · see citing works
mTORC2 affects the maintenance of the muscle stem cell pool
Rion, N., Castets, P., Lin, S., Enderle, L., Reinhard, J. R., & Rüegg, M. A. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0217-y · Cited by 21 · see citing works
Cormerais, Y., Lapp, S. C., Kalafut, K. C., Cissé, M. Y., Shin, J., Stefadu, B., Personnaz, J., Schrotter, S., Freed, J., D’Amore, A., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.05.008 · Cited by 15 · see citing works
Muscle stem cell adaptations to cellular and environmental stress
Gugliuzza, M. V., & Crist, C. G. (2022) · Skeletal Muscle · doi:10.1186/s13395-022-00289-6 · Cited by 20 · see citing works
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 20 · see citing works
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 · see citing works
Southard, S. M., Kim, J.-R., Low, S., Tsika, R. W., & Lepper, C. (2016) · eLife · doi:10.7554/elife.15461 · Cited by 20 · see citing works
Understanding the development of sarcopenic obesity
Gross, D. C., Cheever, C. R., & Batsis, J. A. (2023) · Expert Review of Endocrinology & Metabolism · doi:10.1080/17446651.2023.2267672 · Cited by 19 · see citing works
Microphysiological systems for human aging research
Park, S., Laskow, T. C., Chen, J., Guha, P., Dawn, B., & Kim, D. (2024) · Aging Cell · doi:10.1111/acel.14070 · Cited by 20 · see citing works
Kim, J., Park, I., Shin, H. R., Rhee, J., Seo, J., Jo, Y., Yoo, K., Hann, S., Kang, J., Park, J., et al. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12653 · Cited by 18 · see citing works
Control of topoisomerase II activity and chemotherapeutic inhibition by TCA cycle metabolites
Lee, J. H., Mosher, E. P., Lee, Y., Bumpus, N. N., & Berger, J. M. (2021) · Cell chemical biology · doi:10.1016/j.chembiol.2021.08.014 · Cited by 18 · see citing works
Targeting PKCθ Promotes Satellite Cell Self-Renewal
Benedetti, A., Fiore, P. F., Madaro, L., Lozanoska‐Ochser, B., & Bouché, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072419 · Cited by 17 · see citing works
Scaling of nuclear numbers and their spatial arrangement in skeletal muscle cell size regulation
Hansson, K., & Eftestøl, E. (2023) · Molecular Biology of the Cell · doi:10.1091/mbc.e22-09-0424 · Cited by 17 · see citing works
- Authors
- Brack, A. S., & Muñoz-Cánoves, P.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Brack, Andrew S.
- ORCID
- Brack, Andrew S.
- Venue
- Skeletal Muscle
- Published
- 2015-12
- Volume
- 6
- Issue
- 1
- Pages
- 1-1
- ISSN
- 2044-5040 (ISSN-L)
- PMC
- PMC4716636
- OpenAlex
- W2271088568
- Cited by
- 166
- References
- 76
- Citations by year
- 2026: 12 · 2025: 11 · 2024: 8 · 2023: 18 · 2022: 17 · 2021: 22 · 2020: 19 · 2019: 19 · 2018: 13 · 2017: 11 · 2016: 16
- FWCI
- 1.28
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Skeletal Muscle (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RECERCAT (Consorci de Serveis Universitaris de Catalunya) (publishedVersion, other-oa)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Repositori digital de la UPF (Universitat Pompeu Fabra) (submittedVersion, cc-by)
- Funders
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (RO1AR060868, R01AR061002)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Keywords
- muscle stem cells, satellite cells, aging, skeletal muscle regeneration, parabiosis, stem cell transplantation, extrinsic aging, intrinsic aging, tissue homeostasis, stem cell mobilization
- MeSH terms
- Animals, Cell Differentiation, Humans, Phenotype, Signal Transduction, Cellular Senescence, Muscle, Skeletal, Satellite Cells, Skeletal Muscle, Cell Proliferation, Stem Cell Niche
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 ›
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