Cited by 466Muscle Physiology and DisordersCongenital heart defects researchDevelopmental Biology and Gene Regulation

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Stem cells in postnatal myogenesis: molecular mechanisms of satellite cell quiescence, activation and replenishment

Dhawan, Jyotsna, Rando, Thomas A.·2005·Trends in Cell Biology

DOI 10.1016/j.tcb.2005.10.007

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Abstract

Satellite cells are the primary stem cells in adult skeletal muscle, and are responsible for postnatal muscle growth, hypertrophy and regeneration. In mature muscle, most satellite cells are in a quiescent state, but they activate and begin proliferating in response to extrinsic signals. Following activation, a subset of satellite cell progeny returns to the quiescent state during the process of self-renewal. Here, we review recent studies of satellite cell biology and focus on the key transitions from the quiescent state to the state of proliferative activation and myogenic lineage progression and back to the quiescent state. The molecular mechanisms of these transitions are considered in the context of the biology of the satellite cell niche, changes with age, and interactions with established pathways of myogenic commitment and differentiation.

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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
Muscle Regeneration by Bone Marrow-Derived Myogenic Progenitors
Ferrari, G., Cusella, G., Angelis, D., Coletta, M., Paolucci, E., Stornaiuolo, A., Cossu, G., & Mavilio, F. (1998) · Science · doi:10.1126/science.279.5356.1528 · Cited by 2,721
Cellular and Molecular Regulation of Muscle Regeneration
CHARGÉ, S. B. P., & Rudnicki, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00019.2003 · Cited by 2,691
Pax7 Is Required for the Specification of Myogenic Satellite Cells
Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345
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
Self-citation
Stem Cells
Weissman, I. L. (2000) · Cell · doi:10.1016/s0092-8674(00)81692-x · Cited by 1,827
Myogenic satellite cells: physiology to molecular biology
Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646
Little Evidence for Developmental Plasticity of Adult Hematopoietic Stem Cells
Wagers, A. J., Sherwood, R. I., Christensen, J. L., & Weissman, I. L. (2002) · Science · doi:10.1126/science.1074807 · Cited by 1,460
Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche
Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445
The E2F transcription factor is a cellular target for the RB protein
Chellappan, S., Hiebert, S. W., Mudryj, M. M., Horowitz, J. M., & Nevins, J. R. (1991) · Cell · doi:10.1016/0092-8674(91)90557-f · Cited by 1,415
A Pax3/Pax7-dependent population of skeletal muscle progenitor cells
Relaix, F., Rocancourt, D., Mansouri, A., & BUCKINGHAM, M. E. (2005) · Nature · doi:10.1038/nature03594 · Cited by 1,167
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
Self-citation
The MyoD family and myogenesis: Redundancy, networks, and thresholds
Weintraub, H. (1993) · Cell · doi:10.1016/0092-8674(93)90610-3 · Cited by 1,057
Single-Cell Analysis of Regulatory Gene Expression in Quiescent and Activated Mouse Skeletal Muscle Satellite Cells
Cornelison, D., & Wold, B. J. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8721 · Cited by 934
Muscle satellite cells adopt divergent fates
Zammit, P. S., Golding, J. P., Nagata, Y., Hudon, V., Partridge, T. A., & Beauchamp, J. R. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200312007 · Cited by 924
The formation of skeletal muscle: from somite to limb
BUCKINGHAM, M. E., Bajard, L., Chang, T. H., Daubas, P., Hadchouel, J., Meilhac, S. M., Montarras, D., Rocancourt, D., & Relaix, F. (2003) · Journal of Anatomy · doi:10.1046/j.1469-7580.2003.00139.x · Cited by 918
Expression of Cd34 and Myf5 Defines the Majority of Quiescent Adult Skeletal Muscle Satellite Cells
Beauchamp, J. R., Heslop, L., Yu, D. S., Tajbakhsh, S., Kelly, R. G., Wernig, A., BUCKINGHAM, M. E., Partridge, T. A., & Zammit, P. S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.6.1221 · Cited by 917
The Regulation of Notch Signaling Controls Satellite Cell Activation and Cell Fate Determination in Postnatal Myogenesis
Conboy, I. M., & Rando, T. A. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00254-x · Cited by 905
Self-citation
Biological Progression from Adult Bone Marrow to Mononucleate Muscle Stem Cell to Multinucleate Muscle Fiber in Response to Injury
LaBarge, M. A., & Blau, H. M. (2002) · Cell · doi:10.1016/s0092-8674(02)01078-4 · Cited by 798
Early stages of chick somite development
Christ, B., & Ordahl, C. P. (1995) · Anatomy and Embryology · doi:10.1007/bf00304424 · Cited by 795
Myostatin negatively regulates satellite cell activation and self-renewal
McCroskery, S., Thomas, M., Maxwell, L., Sharma, M., & Kambadur, R. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200207056 · Cited by 784
HGF/SF Is Present in Normal Adult Skeletal Muscle and Is Capable of Activating Satellite Cells
Tatsumi, R., Anderson, J. E., Nevoret, C. J., Halevy, O., & Allen, R. E. (1998) · Developmental Biology · doi:10.1006/dbio.1997.8803 · Cited by 685
A common somitic origin for embryonic muscle progenitors and satellite cells
Gros, J., Manceau, M., Thomé, V., & Marcelle, C. (2005) · Nature · doi:10.1038/nature03572 · Cited by 596
“Sleeping Beauty”: Quiescence in Saccharomyces cerevisiae
Gray, J. V., Petsko, G. A., Johnston, G. C., Ringe, D., Singer, R. A., & Werner‐Washburne, M. (2004) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.68.2.187-206.2004 · Cited by 573
SIGNALING PATHWAYS IN INTESTINAL DEVELOPMENT AND CANCER
Sancho, E., Batlle, E., & Clevers, H. C. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.092805 · Cited by 560
Pax7 directs postnatal renewal and propagation of myogenic satellite cells but not their specification
Oustanina, S., Hause, G., & Braun, T. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600346 · Cited by 531
Skeletal muscle satellite cells
Schultz, E., & McCormick, K. M. (1994) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/bfb0030904 · Cited by 526
Wnt Signaling Induces the Myogenic Specification of Resident CD45+ Adult Stem Cells during Muscle Regeneration
Polesskaya, A., Seale, P., & Rudnicki, M. A. (2003) · Cell · doi:10.1016/s0092-8674(03)00437-9 · Cited by 515
Isolation of Adult Mouse Myogenic Progenitors
Sherwood, R. I., Christensen, J. L., Conboy, I. M., Conboy, M. J., Rando, T. A., Weissman, I. L., & Wagers, A. J. (2004) · Cell · doi:10.1016/j.cell.2004.10.021 · Cited by 491
Self-citation
Cell heterogeneity upon myogenic differentiation: down-regulation of MyoD and Myf-5 generates ‘reserve cells
Yoshida, N., Yoshida, S., Koishi, K., Masuda, K., & Nabeshima, Y.-I. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.6.769 · Cited by 425
Skeletal Myogenic Progenitors Originating from Embryonic Dorsal Aorta Coexpress Endothelial and Myogenic Markers and Contribute to Postnatal Muscle Growth and Regeneration
Angelis, L. D., Berghella, L., Coletta, M., Lattanzi, L., Zanchi, M., Gabriella, M., Ponzetto, C., & Cossu, G. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.4.869 · Cited by 421
Epidermal stem cells: markers, patterning and the control of stem cell fate
Watt, F. M. (1998) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1998.0247 · Cited by 400
Syndecan-3 and Syndecan-4 Specifically Mark Skeletal Muscle Satellite Cells and Are Implicated in Satellite Cell Maintenance and Muscle Regeneration
Cornelison, D., Filla, M. S., Stanley, H. M., Rapraeger, A. C., & Olwin, B. B. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0416 · Cited by 399
Satellite Cell Proliferative Compartments in Growing Skeletal Muscles
Schultz, E. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0097 · Cited by 394
Reversible Expression of CD34 by Murine Hematopoietic Stem Cells
Sato, T., Laver, J. H., & Ogawa, M. (1999) · Blood · doi:10.1182/blood.v94.8.2548.420k38_2548_2554 · Cited by 393
Expression pattern of M‐cadherin in normal, denervated, and regenerating mouse muscles
Irintchev, A., Zeschnigk, M., Starzinski‐Powitz, A., & Wernig, A. (1994) · Developmental Dynamics · doi:10.1002/aja.1001990407 · Cited by 368
Asymmetric Numb distribution is critical for asymmetric cell division of mouse cerebral cortical stem cells and neuroblasts
Shen, Q., Zhong, W., Jan, Y. N., & Temple, S. (2002) · Development · doi:10.1242/dev.129.20.4843 · Cited by 361
Identification of myogenic-endothelial progenitor cells in the interstitial spaces of skeletal muscle
Tamaki, T., Akatsuka, A., Ando, K., Nakamura, Y., Matsuzawa, H., Hotta, T., Roy, R. R., & Edgerton, V. R. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200112106 · Cited by 351
Skeletal muscle satellite cells: Changes in proliferation potential as a function of age
Schultz, E., & Lipton, B. H. (1982) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(82)90105-1 · Cited by 335
Haematopoietic cell-fate decisions, chromatin regulation and ikaros
Georgopoulos, K. (2002) · Nature reviews. Immunology · doi:10.1038/nri747 · Cited by 324
The Muscle Regulatory Factors MyoD and Myf-5 Undergo Distinct Cell Cycle–specific Expression in Muscle Cells
Kitzmann, M., Carnac, G., Vandromme, M., Primig, M., Lamb, N. J. C., & Fernandez, A. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.6.1447 · Cited by 323
Essential and separable roles for Syndecan-3 and Syndecan-4 in skeletal muscle development and regeneration
Cornelison, D. D. W., Wilcox-Adelman, S. A., Goetinck, P. F., Rauvala, H., Rapraeger, A. C., & Olwin, B. B. (2004) · Genes & Development · doi:10.1101/gad.1214204 · Cited by 317
MyoD−/− Satellite Cells in Single-Fiber Culture Are Differentiation Defective and MRF4 Deficient
Cornelison, D., Olwin, B. B., Rudnicki, M. A., & Wold, B. J. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9682 · Cited by 314
Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes
Grounds, M. D., Garrett, K. L., Lai, M. C., Wright, W. E., & Beilharz, M. W. (1992) · Cell & Tissue Research · doi:10.1007/bf00318695 · Cited by 313
E2F4 and E2F5 Play an Essential Role in Pocket Protein–Mediated G1 Control
Gaubatz, S., Lindeman, G. J., Ishida, S., Jakoi, L., Nevins, J. R., Livingston, D. M., & Rempel, R. E. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00071-x · Cited by 302
Temporal expression of myogenic regulatory genes during activation, proliferation, and differentiation of rat skeletal muscle satellite cells
Smith, C. K., Janney, M. J., & Allen, R. E. (1994) · Journal of Cellular Physiology · doi:10.1002/jcp.1041590222 · Cited by 290
Stem cell plasticity
Lakshmipathy, U., & Verfaillie, C. M. (2004) · Blood Reviews · doi:10.1016/j.blre.2004.03.001 · Cited by 264
How is myogenesis initiated in the embryo?
Cossu, G., Tajbakhsh, S., & BUCKINGHAM, M. E. (1996) · Trends in Genetics · doi:10.1016/0168-9525(96)10025-1 · Cited by 234
Crosstalk between cell cycle regulators and the myogenic factor MyoD in skeletal myoblasts
Kitzmann, M., & Fernandez, A. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000882 · Cited by 226
Satellite cell proliferation and the expression of myogenin and desmin in regenerating skeletal muscle: evidence for two different populations of satellite cells.
Rantanen, J., Hurme, T., Lukka, R., Heino, J., & Kalimo, H. (1995) · PubMed · Cited by 223
Regulation of quiescence in lymphocytes
Yusuf, I., & Fruman, D. A. (2003) · Trends in Immunology · doi:10.1016/s1471-4906(03)00141-8 · Cited by 217
Fibroblast Growth Factor Promotes Recruitment of Skeletal Muscle Satellite Cells in Young and Old Rats
Yablonka‐Reuveni, Z., Seger, R., & Rivera, A. J. (1999) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215549904700104 · Cited by 215
Gene Expression Patterns of the Fibroblast Growth Factors and Their Receptors During Myogenesis of Rat Satellite Cells
Kästner, S., Elias, M. C., Rivera, A. J., & Yablonka‐Reuveni, Z. (2000) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540004800805 · Cited by 214
Molecular and cell biology of skeletal muscle regeneration
Grounds, M. D., & Yablonka‐Reuveni, Z. (1993) · Springer eBooks · doi:10.1007/978-94-011-1528-5_9 · Cited by 196
Asymmetric segregation of Numb: a mechanism for neural specification from Drosophila to mammals
Cayouette, M., & RAFF, M. C. (2002) · Nature Neuroscience · doi:10.1038/nn1202-1265 · Cited by 195
Purification and cell-surface marker characterization of quiescent satellite cells from murine skeletal muscle by a novel monoclonal antibody
Fukada, S., Higuchi, S., Segawa, M., Koda, K.-I., Yamamoto, Y., Tsujikawa, K., Kohama, Y., Uezumi, A., Imamura, M., Miyagoe‐Suzuki, Y., et al. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.02.018 · Cited by 190
Myogenic stem cell function is impaired in mice lacking the forkhead /winged helix protein MNF
Garry, D. J., Meeson, A. P., Elterman, J. B., Zhao, Y., Yang, P., Bassel‐Duby, R., & Williams, R. S. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.100501197 · Cited by 165
Persistent Expression of MNF Identifies Myogenic Stem Cells in Postnatal Muscles
Garry, D. J., Yang, Q., Bassel‐Duby, R., & Williams, R. S. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8657 · Cited by 145
Skeletal muscle satellite cells appear during late chicken embryogenesis
Hartley, R. S., Bandman, E., & Yablonka‐Reuveni, Z. (1992) · Developmental Biology · doi:10.1016/0012-1606(92)90106-q · Cited by 133
Regulation of MyoD function in the dividing myoblast
Wei, Q., & Paterson, B. M. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)02120-2 · Cited by 113
p21 is essential for normal myogenic progenitor cell function in regenerating skeletal muscle
Hawke, T. J., Meeson, A. P., Jiang, N., Graham, S. M., Hutcheson, K. A., DiMaio, J. M., & Garry, D. J. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00055.2003 · Cited by 110
Direct inhibition of G1 cdk kinase activity by MyoD promotes myoblast cell cycle withdrawal and terminal differentiation
Zhang, J., Zhao, X., Wei, Q., & Paterson, B. M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.24.6983 · Cited by 104
Activation of Skeletal Muscle Satellite Cells and the Role of Fibroblast Growth Factor Receptors
Johnson, S., & Allen, R. E. (1995) · Experimental Cell Research · doi:10.1006/excr.1995.1251 · Cited by 103
Temporal appearance of satellite cells during myogenesis
Feldman, J. L., & Stockdale, F. E. (1992) · Developmental Biology · doi:10.1016/0012-1606(92)90107-r · Cited by 87
Cell Fusion in Skeletal Muscle: Central Role of NFATC2 in Regulating Muscle Cell Size
Pavlath, G. K., & Horsley, V. (2003) · Cell Cycle · doi:10.4161/cc.2.5.497 · Cited by 81
Modulation of acto-myosin contractility in skeletal muscle myoblasts uncouples growth arrest from differentiation
Dhawan, J., & Helfman, D. M. (2004) · Journal of Cell Science · doi:10.1242/jcs.01197 · Cited by 80
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Anchorage-dependent control of muscle-specific gene expression in C2C12 mouse myoblasts
Milasincic, D. J., Dhawan, J., & Farmer, S. R. (1996) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/bf02723040 · Cited by 74
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Tajbakhsh, S. (2005) · Experimental Cell Research · doi:10.1016/j.yexcr.2005.03.033 · Cited by 70
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Authors: Dhawan, J., & Rando, T. A.
Affiliations: Centre for Cellular and Molecular Biology (IN)
VA Palo Alto Health Care System (US)
Corresponding author: Rando, Thomas A.
ORCID: Dhawan, Jyotsna
Rando, Thomas A.
Venue: Trends in Cell Biology
Publisher: Elsevier BV
Published: 2005-12
Volume: 15
Issue: 12
Pages: 666-673
ISSN: 0962-8924 (ISSN-L)
DOI: 10.1016/j.tcb.2005.10.007
OpenAlex: W2054692433
Cited by: 466
References: 78
Citations by year: 2026: 7 · 2025: 10 · 2024: 6 · 2023: 18 · 2022: 16 · 2021: 22 · 2020: 18 · 2019: 18 · 2018: 11 · 2017: 26 · 2016: 18 · 2015: 25 · 2014: 27 · 2013: 34 · 2012: 40
FWCI: 2.18
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Trends in Cell Biology (publishedVersion)
PubMed (publishedVersion)
Funders: Wellcome Trust
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 › Molecular Biology › Developmental Biology and Gene Regulation
Keywords: satellite cells, skeletal muscle stem cells, quiescence, cell activation, self-renewal, muscle regeneration, muscle hypertrophy, aging, myogenesis
MeSH terms: Animals, Cell Cycle, Cell Differentiation, Humans, Stem Cells, Gene Expression Regulation, Developmental, Muscle Development, Satellite Cells, Skeletal Muscle, Cell Proliferation

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Stem cells in postnatal myogenesis: molecular mechanisms of satellite cell quiescence, activation and replenishment

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