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Molecular Signature of Quiescent Satellite Cells in Adult Skeletal Muscle
Abstract
Skeletal muscle satellite cells play key roles in postnatal muscle growth and regeneration. To study molecular regulation of satellite cells, we directly prepared satellite cells from 8- to 12-week-old C57BL/6 mice and performed genome-wide gene expression analysis. Compared with activated/cycling satellite cells, 507 genes were highly upregulated in quiescent satellite cells. These included negative regulators of cell cycle and myogenic inhibitors. Gene set enrichment analysis revealed that quiescent satellite cells preferentially express the genes involved in cell-cell adhesion, regulation of cell growth, formation of extracellular matrix, copper and iron homeostasis, and lipid transportation. Furthermore, reverse transcription-polymerase chain reaction on differentially expressed genes confirmed that calcitonin receptor (CTR) was exclusively expressed in dormant satellite cells but not in activated satellite cells. In addition, CTR mRNA is hardly detected in nonmyogenic cells. Therefore, we next examined the expression of CTR in vivo. CTR was specifically expressed on quiescent satellite cells, but the expression was not found on activated/proliferating satellite cells during muscle regeneration. CTR-positive cells reappeared at the rim of regenerating myofibers in later stages of muscle regeneration. Calcitonin stimulation delayed the activation of quiescent satellite cells. Our data provide roles of CTR in quiescent satellite cells and a solid scaffold to further dissect molecular regulation of satellite cells. Disclosure of potential conflicts of interest is found at the end of this article.
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“the signature reveals the downregulation of genes that are involved in DNA replication and cell cycle progression.”
From Molecular regulation of stem cell quiescence (2013) · cites this paper as [15]
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“Examples of genes that are downregulated in all three quiescent cell types (HSCs, MuSCs and HFSCs) include genes encoding cyclin A2, cyclin B1, cyclin E2 and survivin”
From Molecular regulation of stem cell quiescence (2013) · cites this paper as [15]
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“a comparison of gene expression profiles of different types of quiescent stem cells, including HSCs45, MuSCs15 and HFSCs43, reveals a gene signature that is common to these quiescent stem cells (TABLE 1).”
From Molecular regulation of stem cell quiescence (2013) · cites this paper as [15]
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Cites
Gene Ontology: tool for the unification of biology
Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., Davis, A. P., Dolinski, K., Dwight, S. S., Eppig, J. T., et al. (2000) · Nature Genetics · doi:10.1038/75556 · Cited by 43,206
Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197
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
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
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
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
Myostatin, a Negative Regulator of Muscle Growth, Functions by Inhibiting Myoblast Proliferation
Thomas, M., Langley, B., Berry, C., Sharma, M., Kirk, S., Bass, J., & Kambadur, R. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m004356200 · Cited by 1,014
Cornelison, D., & Wold, B. J. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8721 · Cited by 934
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
Flagged first, then by citations
Research works printed but not linked: 1
- Bischoff, 2004, Myology, 66
Cited by
Sorted by citations
Items 201–300 of 508
Histone H3.3 sub-variant H3mm7 is required for normal skeletal muscle regeneration
Harada, A., Maehara, K., Ono, Y., Taguchi, H., Yoshioka, K., Kitajima, Y., Xie, Y., Sato, Y., Iwasaki, T., Nogami, J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03845-1 · Cited by 38
Dormancy and Quiescence of Skeletal Muscle Stem Cells
Rocheteau, P., Vinet, M., & Chrétien, F. C. (2014) · Results and problems in cell differentiation · doi:10.1007/978-3-662-44608-9_10 · Cited by 35
Sphingosine-1-phosphate receptor 3 influences cell cycle progression in muscle satellite cells
Fortier, M., Figeac, N., White, R. B., Knopp, P., & Zammit, P. S. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.07.006 · Cited by 34
Human satellite cells: identification on human muscle fibres
Boldrin, L., & Morgan, J. E. (2012) · PLoS Currents · doi:10.1371/currents.rrn1294 · Cited by 33
Ferrer‐Lorente, R., Béjar, M. T., & Badimón, L. (2014) · Stem Cells and Development · doi:10.1089/scd.2014.0070 · Cited by 35
Fujimaki, S., Machida, M., Hidaka, R., Asashima, M., Takemasa, T., & Kuwabara, T. (2013) · Stem Cells International · doi:10.1155/2013/420164 · Cited by 35
Choo, H. J., Canner, J. P., Vest, K. E., Thompson, Z., & Pavlath, G. K. (2017) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00119.2017 · Cited by 33
Visualization of PAX7 protein dynamics in muscle satellite cells in a YFP knock-in-mouse line
Kitajima, Y., & Ono, Y. (2018) · Skeletal Muscle · doi:10.1186/s13395-018-0174-x · Cited by 33
Price, F. D., Matyas, M. N., Gehrke, A. R., Chen, W., Wolin, E., Holton, K. M., Gibbs, R. M., Lee, A. E., Singu, P. S., Sakakeeny, J. S., et al. (2024) · Nature Biotechnology · doi:10.1038/s41587-024-02344-7 · Cited by 29
Wookey, P. J., McLean, C., Hwang, P. Y. K., Furness, S. G. B., Nguyen, S., Kourakis, A., Hare, D. L., & Rosenfeld, J. V. (2012) · Histopathology · doi:10.1111/j.1365-2559.2011.04146.x · Cited by 30
From cyclins to CDKIs: Cell cycle regulation of skeletal muscle stem cell quiescence and activation
Mademtzoglou, D., & Relaix, F. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2022.113275 · Cited by 32
Nicoletti, C., Wei, X., Etxaniz, U., D’Ercole, C., Madaro, L., Perera, R. J., & Puri, P. (2023) · iScience · doi:10.1016/j.isci.2023.107114 · Cited by 31
Lowering circulating apolipoprotein E levels improves aged bone fracture healing
Rong, H., Zong, X., Nadesan, P., Huebner, J. L., Kraus, V. B., White, J. P., White, P. J., & Baht, G. S. (2019) · JCI Insight · doi:10.1172/jci.insight.129144 · Cited by 29
Granet, J. A., Robertson, R., Cusmano, A. A., Filippelli, R. L., Lorenz, T. O., Li, S., Yaqubi, M., Stratton, J. A., & Chang, N. C. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07755-1 · Cited by 28
Transcriptional networks that regulate muscle stem cell function
Punch, V. G., Jones, A., & Rudnicki, M. A. (2009) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.11 · Cited by 29
Regulation of myoblast differentiation by metabolic perturbations induced by metformin
Pavlidou, T., Rosina, M., Fuoco, C., Gerini, G., Gargioli, C., Castagnoli, L., & Cesareni, G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182475 · Cited by 29
Core Transcription Factors Promote Induction of PAX3-Positive Skeletal Muscle Stem Cells
Sato, T., Higashioka, K., Sakurai, H., Yamamoto, T., Goshima, N., Ueno, M., & Sotozono, C. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.06.006 · Cited by 31
Sun, C., Kannan, S., Choi, I. Y., Lim, H., Zhang, H., Chen, G. S., Zhang, N., Park, S., Serra, C., Iyer, S. R., et al. (2022) · Cell stem cell · doi:10.1016/j.stem.2022.03.004 · Cited by 28
High‐wire act: the poised genome and cellular memory
Puri, D., Gala, H., Mishra, R. K., & Dhawan, J. (2014) · FEBS Journal · doi:10.1111/febs.13165 · Cited by 26
Mimicking Muscle Stem Cell Quiescence in Culture: Methods for Synchronization in Reversible Arrest
Arora, R., Rumman, M., Venugopal, N., Gala, H., & Dhawan, J. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_15 · Cited by 28
Meng, J., Zou, X., Wu, R., Zhong, R., Zhu, D., & Zhang, Y. (2014) · Protein & Cell · doi:10.1007/s13238-014-0025-4 · Cited by 28
Matos, A. M., Gomes‐Duarte, A., Faria, M., Barros, P., Jordan, P., Amaral, M. D., & Matos, P. (2018) · Scientific Reports · doi:10.1038/s41598-018-31514-2 · Cited by 29
The satellite cell in skeletal muscle: A story of heterogeneity
Guilhot, C., Catenacci, M., Lofaro, S., & Rudnicki, M. A. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.01.018 · Cited by 27
“Ins” and “Outs” of mesenchymal stem cell osteogenesis in regenerative medicine
Yamaguchi, D. T. (2014) · World Journal of Stem Cells · doi:10.4252/wjsc.v6.i2.94 · Cited by 29
Wang, J., Broer, T., Chavez, T., Zhou, C. J., Tran, S., Xiang, Y., Khodabukus, A., Diao, Y., & Bursac, N. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121508 · Cited by 28
Regulation of Cell Cycle Entry and Exit: A Single Cell Perspective
Coller, H. A. (2019) · Comprehensive physiology · doi:10.1002/cphy.c190014 · Cited by 33
Recruiting endogenous stem cells: a novel therapeutic approach for erectile dysfunction
Xin, Z., Xu, Y., Lin, G., Lue, T., & Guo, Y. (2015) · Asian Journal of Andrology · doi:10.4103/1008-682x.150040 · Cited by 27
Arpke, R. W., & Kyba, M. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3810-0_12 · Cited by 25
Arjona, M., Goshayeshi, A., Rodríguez-Mateo, C., Brett, J. O., Both, P., Ishak, H. D., & Rando, T. A. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.11.012 · Cited by 25
Quiescence of human muscle stem cells is favored by culture on natural biopolymeric films
Monge, C., Distasio, N., Rossi, T., Sébastien, M., Sakai, H., Kalman, B., Boudou, T., Tajbakhsh, S., Marty, I., Bigot, A., et al. (2017) · Stem Cell Research & Therapy · doi:10.1186/s13287-017-0556-8 · Cited by 25
Heterocellular molecular contacts in the mammalian stem cell niche
Ceafalan, L. C., Enciu, A., Fertig, T. E., Popescu, B. O., Gherghiceanu, M., Hinescu, M. E., & Radu, E. (2018) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2018.07.001 · Cited by 27
Siegel, A. L., Gurevich, D., & Currie, P. D. (2013) · FEBS Journal · doi:10.1111/febs.12300 · Cited by 24
Isolation of Muscle Stem Cells from Mouse Skeletal Muscle
Gayraud-Morel, B., Pala, F., Sakai, H., & Tajbakhsh, S. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_2 · Cited by 24
Sepsis-Induced Myopathy and Gut Microbiome Dysbiosis: Mechanistic Links and Therapeutic Targets
Mankowski, R. T., Laitano, O., Darden, D. B., Kelly, L. S., Munley, J. A., Loftus, T. J., Mohr, A. M., Efron, P. A., & Thomas, R. M. (2021) · Shock · doi:10.1097/shk.0000000000001843 · Cited by 25
Arpke, R. W., Shams, A. S., Collins, B. C., Larson, A. A., Lu, N., Lowe, D. A., & Kyba, M. (2021) · Skeletal Muscle · doi:10.1186/s13395-021-00277-2 · Cited by 25
Specific pattern of cell cycle during limb fetal myogenesis
de Lima, J. E., Bonnin, M.-A., Bourgeois, A., Parisi, A., Grand, F. L., & Duprez, D. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.05.015 · Cited by 24
Detection of Quiescent Radioresistant Epithelial Progenitors in the Adult Thymus
Dumont-Lagacé, M., Gerbe, H., Daouda, T., Laverdure, J., Brochu, S., Lemieux, S., Gagnon, É., & Perreault, C. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01717 · Cited by 22
Cadherin-dependent adhesion is required for muscle stem cell niche anchorage and maintenance
Hung, M., Lo, H.-F., Beckmann, A. G., Demircioğlu, D., Damle, G., Hasson, D., Radice, G. L., & Krauss, R. S. (2024) · Development · doi:10.1242/dev.202387 · Cited by 23
Lactate Metabolism and Satellite Cell Fate
Nalbandian, M., Radak, Z. O., & Takeda, M. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.610983 · Cited by 27
Molecular regulation of satellite cells via intercellular signaling
Yeh, C.-J., Sattler, K. M., & Lepper, C. (2023) · Gene · doi:10.1016/j.gene.2023.147172 · Cited by 26
The avian embryo as a model system for skeletal myogenesis.
Hirst, C., & Marcelle, C. (2015) · Results and problems in cell differentiation · doi:10.1007/978-3-662-44608-9_5 · Cited by 25
Group I Paks support muscle regeneration and counteract cancer‐associated muscle atrophy
Perpetuini, A. C., Cecconi, A. D. R., Chiappa, M., Martinelli, G. B., Fuoco, C., Desiderio, G., Castagnoli, L., Gargioli, C., Piccirillo, R., & Cesareni, G. (2018) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12303 · Cited by 24
Developmental Origins of Fusion-Negative Rhabdomyosarcomas
Kikuchi, K., Rubin, B. P., & Keller, C. (2011) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385940-2.00002-4 · Cited by 24
Yamaguchi, M., Ogawa, R., Watanabe, Y., Uezumi, A., Miyagoe‐Suzuki, Y., Tsujikawa, K., Yamamoto, H., Takeda, S., & Fukada, S. (2012) · Journal of Molecular Histology · doi:10.1007/s10735-012-9421-3 · Cited by 22
Self-citationFrailty and Rejuvenation with Stem Cells: Therapeutic Opportunities and Clinical Challenges
Sun, X., Hao, Q., Tang, R.-J., Xiao, C., Ge, M., & Dong, B. (2019) · Rejuvenation Research · doi:10.1089/rej.2017.2048 · Cited by 22
Reed, K. M., Mendoza, K. M., Abrahante, J. E., Barnes, N., Velleman, S. G., & Strasburg, G. M. (2017) · BMC Genomics · doi:10.1186/s12864-017-3740-4 · Cited by 22
Sfyri, P. P., Yuldasheva, N. Y., Tzimou, A., Giallourou, N., Crispi, V., Aburima, A. A., Beltrán-Álvarez, P., Patel, K., Mougios, V., Swann, J. R., et al. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.10.422 · Cited by 22
Παπανικολάου, Κ., Veskoukis, A. S., Draganidis, D., Baloyiannis, I., Deli, C. K., Poulios, A., Jamurtas, A. Z., & Fatouros, I. G. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.001 · Cited by 22
Muscle injury causes long-term changes in stem-cell DNA methylation
Michaeli, T. F., Sabag, O., Fok, R., Azria, B., Monin, J., Nevo, Y., Gielchinsky, Y., Berman, B. P., Cedar, H., & Bergman, Y. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2212306119 · Cited by 23
He, Y., Heng, Y., Qin, Z., Wei, X., Wu, Z., & Qu, J. Y. (2023) · Science Advances · doi:10.1126/sciadv.adi1891 · Cited by 21
Genome Editing and Muscle Stem Cells as a Therapeutic Tool for Muscular Dystrophies
Pini, V., Morgan, J. E., Francesco Muntoni, A., & O’Neill, H. C. (2017) · Current Stem Cell Reports · doi:10.1007/s40778-017-0076-6 · Cited by 20
TMEM8C-mediated fusion is regionalized and regulated by NOTCH signalling during foetal myogenesis
de Lima, J. E., Blavet, C., Bonnin, M.-A., Hirsinger, E., Havis, E., Relaix, F., & Duprez, D. (2022) · Development · doi:10.1242/dev.199928 · Cited by 20
Swiderski, K., Thakur, S. S., Naim, T., Trieu, J., Chee, A., Stapleton, D., Koopman, R., & Lynch, G. S. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0108-4 · Cited by 21
A Three-Dimensional Culture Model of Reversibly Quiescent Myogenic Cells
Aguanno, S., Petrelli, C., Siena, S. D., Angelis, L. D., Pellegrini, M., & Naro, F. (2019) · Stem Cells International · doi:10.1155/2019/7548160 · Cited by 19
Southard, S. M., Kim, J.-R., Low, S., Tsika, R. W., & Lepper, C. (2016) · eLife · doi:10.7554/elife.15461 · Cited by 20
Induction of Skeletal Muscle Progenitors and Stem Cells from human induced Pluripotent Stem Cells
Sato, T. (2020) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-200497 · Cited by 19
Jang, Y., Kang, S., Han, H. H., Kim, B. G., & Cho, N. H. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-01858-y · Cited by 19
Applications of skeletal muscle progenitor cells for neuromuscular diseases.
Hosoyama, T., Dyke, J. V., & Suzuki, M. (2012) · Europe PMC (PubMed Central) · Cited by 19
Simultaneous Measurement of Mitochondrial and Glycolytic Activity in Quiescent Muscle Stem Cells
Ryall, J. G. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_13 · Cited by 19
Byun, W. S., Lee, J., & Baek, J.-H. (2024) · Inflammation and Regeneration · doi:10.1186/s41232-024-00354-1 · Cited by 20
Exercise/Resistance Training and Muscle Stem Cells
Fukada, S., & Nakamura, A. (2021) · Endocrinology and Metabolism · doi:10.3803/enm.2021.401 · Cited by 20
Self-citationA 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
Feedbacks between size and density determine rapid eco‐phenotypic dynamics
Gibert, J. P., Han, Z., Wieczynski, D. J., Votzke, S., & Yammine, A. (2022) · Functional Ecology · doi:10.1111/1365-2435.14070 · Cited by 18
Mavrommatis, L., Jeong, H., Kindler, U., Gomez-Giro, G., Kienitz, M., Stehling, M., Psathaki, O. E., Zeuschner, D., Bixel, M. G., Han, D., et al. (2020) · bioRxiv · doi:10.1101/2020.09.14.295832 · Cited by 48
Liu, L. A., Rodríguez-Mateo, C., Huang, P., Huang, A., Lieu, A. C., Mao, M., Chung, M., Yang, S., Yu, K., Charville, G. W., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2025281118 · Cited by 21
Ahmad, S. S., Ahmad, K., Lim, J. H., Shaikh, S., Lee, E. J., & Choi, I. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.131411 · Cited by 17
Muscle Satellite Cell Protein Teneurin-4 Regulates Differentiation During Muscle Regeneration
Ishii, K., Suzuki, N., Mabuchi, Y., Ito, N., Kikura, N., Fukada, S., Okano, H., Takeda, S., & Akazawa, C. (2015) · Stem Cells · doi:10.1002/stem.2058 · Cited by 17
Self-citationCCAAT/enhancer binding protein β is required for satellite cell self-renewal
Lala-Tabbert, N., AlSudais, H., Marchildon, F., Fu, D., & Wiper‐Bergeron, N. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0112-8 · Cited by 17
Dong, C., Wang, X., Sun, L., Zhu, L., Yang, D., Gao, S., Zhang, W., Ling, B., Liang, A., Gao, Z., et al. (2022) · Stem Cell Research · doi:10.1016/j.scr.2021.102618 · Cited by 16
Ancel, S., Michaud, J., Sizzano, F., Tauzin, L., Oliveira, M., Migliavacca, E., Schüler, S. C., Raja, S., Dammone, G., Karaz, S., et al. (2024) · Stem Cell Reports · doi:10.1016/j.stemcr.2024.05.005 · Cited by 16
Bioenergetics mechanisms regulating muscle stem cell self-renewal commitment and function
Abreu, P. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.04.036 · Cited by 19
Metabolic regulation in adult and aging skeletal muscle stem cellsPreprint
Sartorelli, V., & Ciuffoli, V. (2024) · Genes & Development · doi:10.1101/gad.352277.124 · Cited by 19
Sex Hormones and Satellite Cell Regulation in Women
Oxfeldt, M., Dalgaard, L. B., Farup, J., & Hansen, M. (2022) · Translational Sports Medicine · doi:10.1155/2022/9065923 · Cited by 17
Budsuren, U., Ulaangerel, T., Shen, Y., Liu, G., Davshilt, T., Yi, M., Bold, D., Zhang, X., Bai, D., Dorjgotov, D., et al. (2022) · Genes · doi:10.3390/genes13101836 · Cited by 16
Feng, X., Wang, A. H., Juan, A. H., Ko, K. D., Jiang, K., Riparini, G., Ciuffoli, V., Kaba, A., Lopez, C., Naz, F., et al. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.04.005 · Cited by 16
Zfp423 Regulates Skeletal Muscle Regeneration and Proliferation
Addison, W. N., Hall, K. C., Kokabu, S., Matsubara, T., Fu, M. M.-J., Gori, F., & Baron, R. (2019) · Molecular and Cellular Biology · doi:10.1128/mcb.00447-18 · Cited by 15
Feige, P., & Rudnicki, M. A. (2018) · Current Biology · doi:10.1016/j.cub.2018.02.064 · Cited by 15
Fujita, R., & Crist, C. G. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.004 · Cited by 16
Dynamic transcriptome profiles of postnatal porcine skeletal muscle growth and development
Wang, Y., Wang, J., Hu, H., Wang, H., Wang, C., Lin, H., & Zhao, X. (2021) · BMC Genomic Data · doi:10.1186/s12863-021-00984-1 · Cited by 17
Wookey, P. J., Turner, K. N., & Furness, J. B. (2012) · Cell and Tissue Research · doi:10.1007/s00441-011-1303-6 · Cited by 15
Satellite Cells: Regenerative Mechanisms and Applicability in Muscular Dystrophy
de Souza, G. T., Zanette, R. D. S. S., do Amaral, D. L. A. S., da Guia, F. C., Maranduba, C. P., de Souza, C. M., Guimarães, E. D. S. G., Rettore, J. V. P., Rabelo, N. C., do Carmo, A. M. R., et al. (2015) · Stem Cells International · doi:10.1155/2015/487467 · Cited by 14
Berg, Z., Beffa, L. R., Cook, D. P., & Cornelison, D. (2011) · Neuromuscular Disorders · doi:10.1016/j.nmd.2010.12.009 · Cited by 14
Transplantation of Skeletal Muscle Stem Cells
Hall, M. N., Hall, J. K., Cadwallader, A. B., Pawlikowski, B. T., Doles, J. D., Elston, T. L., & Olwin, B. B. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_12 · Cited by 14
Myogenic Satellite Cells: Biological Milieu and Possible Clinical Applications
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Gala, H., Saha, D., Venugopal, N., Aloysius, A., Purohit, G., & Dhawan, J. (2022) · Journal of Cell Science · doi:10.1242/jcs.259789 · Cited by 17
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Self-citationShelton, M., Ritso, M., Liu, J., O’Neil, D., Kocharyan, A., Rudnicki, M. A., Stanford, W. L., Skerjanc, I. S., & Blais, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0222946 · Cited by 12
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Metadata
- Authors
- Fukada, S.-I., Uezumi, A., Ikemoto, M., Masuda, S., Segawa, M., Tanimura, N., Yamamoto, H., Miyagoe-Suzuki, Y., & Takeda, S.
- Affiliations
- National Center of Neurology and Psychiatry (JP)
- Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan
- The University of Osaka (JP)
- Mizuho Research & Technologies, Ltd. (Japan) (JP)
- Venue
- Stem Cells
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-06-28
- Volume
- 25
- Issue
- 10
- Pages
- 2448-2459
- ISSN
- 1066-5099 (ISSN-L)
- 1549-4918
- OpenAlex
- W2122795085
- Cited by
- 506
- References
- 45
- Citations by year
- 2026: 14 · 2025: 20 · 2024: 34 · 2023: 26 · 2022: 35 · 2021: 32 · 2020: 37 · 2019: 36 · 2018: 31 · 2017: 35 · 2016: 31 · 2015: 32 · 2014: 23 · 2013: 27 · 2012: 33
- FWCI
- 5.16
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Stem Cells (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Society for the Promotion of Science (14657158)
- 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, calcitonin receptor, skeletal muscle regeneration, satellite cell activation, gene expression profiling, cell cycle regulation, cell-cell adhesion, extracellular matrix, lipid transport
- MeSH terms
- Animals, Calcitonin, Cell Differentiation, Cell Division, Female, Mice, Inbred C57BL, Muscle Proteins, Regeneration, RNA, Messenger, Biomarkers, Cell Adhesion Molecules, Receptors, Calcitonin, Myogenic Regulatory Factors, Muscle, Skeletal, Gene Expression Regulation, Developmental, Cell Cycle Proteins, Gene Expression Profiling, Muscle Development, Satellite Cells, Skeletal Muscle, Apoptosis Regulatory Proteins, Mice
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