FOXO3 Promotes Quiescence in Adult Muscle Stem Cells during the Process of Self-Renewal
Open accessAbstract
Skeletal muscle stem cells, or "satellite cells" (SCs), are required for the regeneration of damaged muscle tissue. Although SCs self-renew during regeneration, the mechanisms that govern SC re-entry into quiescence remain elusive. We show that FOXO3, a member of the forkhead family of transcription factors, is expressed in quiescent SCs (QSCs). Conditional deletion of Foxo3 in QSCs impairs self-renewal and increases the propensity of SCs to adopt a differentiated fate. Transcriptional analysis of SCs lacking FOXO3 revealed a downregulation of Notch signaling, a key regulator of SC quiescence. Conversely, overexpression of Notch intracellular domain (NICD) rescued the self-renewal deficit of FOXO3-deficient SCs. We show that FOXO3 regulates NOTCH1 and NOTCH3 receptor expression and that decreasing expression of NOTCH1 and NOTCH3 receptors phenocopies the effect of FOXO3 deficiency in SCs. We demonstrate that FOXO3, perhaps by activating Notch signaling, promotes the quiescent state during SC self-renewal in adult muscle regeneration.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Constitutive deletion of three of the FOXO genes (FOXO1, FOXO3 and FOXO4) in the MuSC lineage during development results in the impairment of postnatal establishment of the MuSC population and a more rapid MuSC depletion with age.
“Consistent with previous reports of the role of FOXO factors in HSC, MuSC and NSC quiescence85–90, constitutive deletion of three of the FOXO genes (FOXO1, FOXO3 and FOXO4) in the MuSC lineage during development results in the impairment of postnatal establishment of the MuSC population and a more rapid MuSC depletion with age32.”
From Ageing and rejuvenation of tissue stem cells and their niches (2023) · cites this paper as [86]
FOXO transcription factors integrate growth factors and stress signal transduction pathways, and may represent a hub for the action of various systemic factors in stem cells in ageing brain, muscle, blood and intestine.
“For example, FOXO transcription factors integrate growth factors and stress signal transduction pathways, and may represent a ‘hub’ for the action of various systemic factors in stem cells in ageing brain, muscle, blood and intestine32,85–90.”
From Ageing and rejuvenation of tissue stem cells and their niches (2023) · cites this paper as [86]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Akt Promotes Cell Survival by Phosphorylating and Inhibiting a Forkhead Transcription Factor
Brunet, A., Bonni, A., Zigmond, M. J., Lin, M. Z., Juo, P., Hu, L. S., Anderson, M. J., Arden, K. C., Blenis, J., & Greenberg, M. E. (1999) · Cell · doi:10.1016/s0092-8674(00)80595-4 · Cited by 6,535 · see citing works
Self-citationCre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121 · 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
Self-citationIncreased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis
Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C., & Rando, T. A. (2007) · Science · doi:10.1126/science.1144090 · Cited by 1,564 · see citing works
Self-citationFoxOs Are Critical Mediators of Hematopoietic Stem Cell Resistance to Physiologic Oxidative Stress
Tothova, Z., Kollipara, R., Huntly, B. J., Lee, B. H., Castrillon, D. H., Cullen, D. E., McDowell, E. P., Lazo-Kallanian, S., Williams, I. R., Sears, C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.01.003 · Cited by 1,562 · 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 · see citing works
FOXO transcription factors at the interface between longevity and tumor suppression
Greer, E. L., & Brunet, A. (2005) · Oncogene · doi:10.1038/sj.onc.1209086 · Cited by 1,306 · see citing works
Self-citationMolecular 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 · see citing works
Self-citationFoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis
Paik, J.-H., Kollipara, R., Chu, G., Ji, H., Xiao, Y., Ding, Z., Miao, L., Tothova, Z., Horner, J. W., Carrasco, D. R., et al. (2007) · Cell · doi:10.1016/j.cell.2006.12.029 · Cited by 1,032 · see citing works
Suppression of Ovarian Follicle Activation in Mice by the Transcription Factor Foxo3a
Castrillón, D. H., Miao, L., Kollipara, R., Horner, J. W., & DePinho, R. A. (2003) · Science · doi:10.1126/science.1086336 · Cited by 956 · see citing works
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 · see citing works
Foxo3a is essential for maintenance of the hematopoietic stem cell pool
Miyamoto, K., Kazuhito, N., & Atsushi, H. (2009) · Kanazawa University Repository for Academic Resources (DSpace) (Kanazawa University) · Cited by 858 · see citing works
Groszer, M., Erickson, R., Scripture-Adams, D. D., Lesche, R., Trumpp, A., Zack, J. A., Kornblum, H. I., Liu, X., & Wu, H. (2001) · Science · doi:10.1126/science.1065518 · Cited by 798 · see citing works
Hosaka, T., Biggs, W., Tieu, D. D., Boyer, A. D., Varki, N. M., Cavenee, W. K., & Arden, K. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400093101 · Cited by 684 · see citing works
Furuyama, T., Nakazawa, T., Nakano, I., & Mori, N. (2000) · Biochemical Journal · doi:10.1042/0264-6021:3490629 · Cited by 672 · see citing works
Mechanisms of Stem Cell Self-Renewal
He, S., Nakada, D., & Morrison, S. J. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113248 · Cited by 607 · see citing works
Notch Signaling Is Necessary to Maintain Quiescence in Adult Muscle Stem Cells
Bjornson, C. R. R., Cheung, T. H., Liu, L., Tripathi, P. V., Steeper, K. M., & Rando, T. A. (2012) · Stem Cells · doi:10.1002/stem.773 · Cited by 598 · see citing works
Self-citationFoxO3 Regulates Neural Stem Cell Homeostasis
Renault, V. M., Rafalski, V. A., Morgan, A. A., Salih, D. A. M., Brett, J. O., Webb, A. E., Villeda, S. A., Thekkat, P. U., Guillerey, C., Denko, N. C., et al. (2009) · Cell Stem Cell · doi:10.1016/j.stem.2009.09.014 · Cited by 586 · see citing works
Self-citationDosage‐sensitive requirement for mouse Dll4 in artery development
Duarte, A., Hirashima, M., Benedito, R., Trindade, A., Diniz, P., Bekman, E., Costa, L., Henrique, D., & Rossant, J. (2004) · Genes & Development · doi:10.1101/gad.1239004 · Cited by 563 · see citing works
Allen, R. E., & Boxhorn, L. K. (1989) · Journal of Cellular Physiology · doi:10.1002/jcp.1041380213 · Cited by 554 · see citing works
Involvement of Foxo transcription factors in angiogenesis and postnatal neovascularization
Potente, M., Urbich, C., Sasaki, K., Hofmann, W. K., Heeschen, C., Aicher, A., Kollipara, R., DePinho, R. A., Zeiher, A. M., & Dimmeler, S. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23126 · Cited by 527 · see citing works
Mourikis, P., Sambasivan, R., Castel, D., Rocheteau, P., Bizzarro, V., & Tajbakhsh, S. (2012) · Stem Cells · doi:10.1002/stem.775 · Cited by 526 · see citing works
Maintenance of muscle stem-cell quiescence by microRNA-489
Cheung, T. H., Quach, N. L., Charville, G. W., Liu, L., Park, L., Edalati, A., Yoo, B., Hoang, P., & Rando, T. A. (2012) · Nature · doi:10.1038/nature10834 · Cited by 461 · see citing works
Self-citationYoshida, 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 · see citing works
Regulation of NF-κB, Th Activation, and Autoinflammation by the Forkhead Transcription Factor Foxo3a
Lin, L., Hron, J. D., & Peng, S. L. (2004) · Immunity · doi:10.1016/j.immuni.2004.06.016 · Cited by 420 · see citing works
McCright, B., Gao, X., Shen, L., Lozier, J., Lan, Y., Maguire, M., Herzlinger, D., Weinmaster, G., Jiang, R., & Gridley, T. (2001) · Development · doi:10.1242/dev.128.4.491 · Cited by 366 · 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
FoxO6, a Novel Member of the FoxO Class of Transcription Factors with Distinct Shuttling Dynamics
Jacobs, F. M. J., van der Heide, L. P., Wijchers, P. J., Burbach, J. P. H., Hoekman, M. F. M., & Smidt, M. P. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302804200 · Cited by 341 · see citing works
Acetylcholine receptors and myasthenia
Lindstrom, J. M. (2000) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(200004)23:4 · Cited by 277 · see citing works
Wen, Y., Bi, P., Liu, W., Asakura, A., Keller, C., & Kuang, S. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.06753-11 · Cited by 271 · see citing works
Troy, A., Cadwallader, A. B., Fedorov, Y., Tyner, K., Tanaka, K. K., & Olwin, B. B. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.05.025 · Cited by 268 · see citing works
Autocrine and Paracrine Angiopoietin 1/Tie-2 Signaling Promotes Muscle Satellite Cell Self-Renewal
Abou-Khalil, R., Grand, F. L., Pallafacchina, G., Valable, S., Authier, F., Rudnicki, M. A., Gherardi, R. K., Germain, S., Chrétien, F. C., Sotiropoulos, A., et al. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.06.001 · Cited by 236 · see citing works
Regulation of FOXO protein stability via ubiquitination and proteasome degradation
Huang, H., & Tindall, D. J. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.01.007 · Cited by 227 · see citing works
FOXO transcription factors: key regulators of cell fate
Lam, E. W. ‐., Francis, R. E., & Petković, M. (2006) · Biochemical Society Transactions · doi:10.1042/bst0340722 · Cited by 214 · see citing works
Inflammatory arthritis requires Foxo3a to prevent Fas ligand–induced neutrophil apoptosis
Jonsson, A. H., Allen, P. M., & Peng, S. L. (2005) · Nature Medicine · doi:10.1038/nm1248 · Cited by 214 · see citing works
Prospective Isolation of Skeletal Muscle Stem Cells with a Pax7 Reporter
Bosnakovski, D., Xu, Z., Li, W., Thet, S., Cleaver, O., Perlingeiro, R. C. R., & Kyba, M. (2008) · Stem Cells · doi:10.1634/stemcells.2007-1017 · Cited by 187 · see citing works
FOXO3 shares common targets with ASCL1 genome-wide and inhibits ASCL1-dependent neurogenesis
Webb, A. E., Pollina, E. A., Vierbuchen, T., Urbán, N., Ucar, D., Leeman, D. S., Martynoga, B., Sewak, M., Rando, T. A., Guillemot, F., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.06.035 · Cited by 164 · see citing works
Self-citationCodependent Activators Direct Myoblast-Specific MyoD Transcription
Hu, P., Geles, K. G., Paik, J.-H., DePinho, R. A., & Tjian, R. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.08.018 · Cited by 155 · see citing works
Regenerating skeletal muscle cells express insulin‐like growth factor I
Jennische, E., & Hansson, H. (1987) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1987.tb08144.x · Cited by 140 · see citing works
Biomarker system for studying muscle, stem cells, and cancer in vivo
Nishijo, K., Hosoyama, T., Bjornson, C. R. R., Schaffer, B. S., Prajapati, S. I., Bahadur, A. N., Hansen, M. S. T., Blandford, M. C., McCleish, A. T., Rubin, B. P., et al. (2009) · The FASEB Journal · doi:10.1096/fj.08-128116 · Cited by 132 · see citing works
Self-citationRole of the basement membrane in the regeneration of skeletal muscle
Caldwell, C., Mattey, D. L., & Weller, R. (1990) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1990.tb01159.x · Cited by 115 · see citing works
Six1 regulates stem cell repair potential and self-renewal during skeletal muscle regeneration
Grand, F. L., Grifone, R., Mourikis, P., Houbron, C., Gigaud, C., Pujol, J., Maillet, M., Pagès, G., Rudnicki, M. A., Tajbakhsh, S., et al. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201201050 · Cited by 113 · see citing works
van der Heide, L. P., Jacobs, F. M. J., Burbach, J. P. H., Hoekman, M. F. M., & Smidt, M. P. (2005) · Biochemical Journal · doi:10.1042/bj20050525 · Cited by 110 · see citing works
Lee, H.-Y., Chung, J.-W., Youn, S.-W., Kim, J.-Y., Park, K.-W., Koo, B.-K., Oh, B.-H., Park, Y.-B., Chaqour, B., Walsh, K., et al. (2007) · Circulation Research · doi:10.1161/01.res.0000257945.97958.77 · Cited by 107 · see citing works
Heslop, L., Beauchamp, J. R., Tajbakhsh, S., BUCKINGHAM, M. E., Partridge, T. A., & Zammit, P. S. (2001) · Gene Therapy · doi:10.1038/sj.gt.3301463 · Cited by 100 · see citing works
Notch Signaling Suppresses p38 MAPK Activity via Induction of MKP-1 in Myogenesis
Kondoh, K., Sunadome, K., & Nishida, E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607630200 · Cited by 91 · see citing works
Foxo3a is essential for maintenance of the hematopoietic stem cell pool.
Miyamoto, K., Araki, K. Y., Naka, K., Arai, F., Takubo, K., Yamazaki, S., Matsuoka, S., Miyamoto, T., Ito, K., Ohmura, M., et al. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.02.001 · Cited by 41 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
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
Satellite Cells and Skeletal Muscle Regeneration
Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive Physiology · doi:10.1002/cphy.c140068 · Cited by 719 · see citing works
Skeletal muscle: A review of molecular structure and function, in health and disease
Mukund, K., & Subramaniam, S. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1462 · Cited by 680 · see citing works
AMPK in skeletal muscle function and metabolism
Kjøbsted, R., Hingst, J. R., Fentz, J., Foretz, M., Sanz, M.-N., Pehmøller, C. K., Shum, M., Marette, A., Mounier, R., Treebak, J. T., et al. (2017) · The FASEB Journal · doi:10.1096/fj.201700442r · Cited by 496 · see citing works
Intrinsic and extrinsic mechanisms regulating satellite cell function
Dumont, N. A., Wang, Y. X., & Rudnicki, M. A. (2015) · Development · doi:10.1242/dev.114223 · Cited by 491 · see citing works
Mitochondria as Signaling Organelles Control Mammalian Stem Cell Fate
Chakrabarty, R. P., & Chandel, N. S. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.02.011 · Cited by 490 · see citing works
Control of satellite cell function in muscle regeneration and its disruption in ageing
Sousa-Victor, P., García-Prat, L., & Muñoz-Cánoves, P. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00421-2 · Cited by 476 · see citing works
The central role of muscle stem cells in regenerative failure with aging
Blau, H. M., Cosgrove, B. D., & Ho, A. T. V. (2015) · Nature Medicine · doi:10.1038/nm.3918 · Cited by 437 · see citing works
Ageing and rejuvenation of tissue stem cells and their niches
Brunet, A., Goodell, M. A., & Rando, T. A. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00510-w · Cited by 407 · see citing works
Self-citation<b><i>FOXO3:</i></b> A Major Gene for Human Longevity - A Mini-Review
Morris, B. J., Willcox, D. C., Donlon, T. A., & Willcox, B. J. (2015) · Gerontology · doi:10.1159/000375235 · Cited by 353 · see citing works
Molecular circuitry of stem cell fate in skeletal muscle regeneration, ageing and disease
Almada, A. E., & Wagers, A. J. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.7 · Cited by 314 · see citing works
Regulation of Stem Cell Aging by Metabolism and Epigenetics
Ren, R., Ocampo, A., Liu, G., & Belmonte, J. C. I. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.07.019 · Cited by 269 · see citing works
Molecular Biomarkers for Embryonic and Adult Neural Stem Cell and Neurogenesis
Zhang, J., & Jiao, J. (2015) · BioMed Research International · doi:10.1155/2015/727542 · Cited by 270 · see citing works
Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
de Morrée, A., & Rando, T. A. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00568-6 · Cited by 243 · see citing works
Self-citationFOXO transcription factors as mediators of stress adaptation
Colman, M. J. R., Dansen, T. B., & Burgering, B. M. T. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00649-0 · Cited by 225 · see citing works
Vieira, M. S., Santos, A. K., Vasconcellos, R., Goulart, V. A. M., Parreira, R. C., Kihara, A. H., Ulrich, H., & Resende, R. R. (2018) · Biotechnology Advances · doi:10.1016/j.biotechadv.2018.08.002 · Cited by 191 · see citing works
Characterization of the direct targets of<scp>FOXO</scp>transcription factors throughout evolution
Webb, A. E., Kundaje, A., & Brunet, A. (2016) · Aging Cell · doi:10.1111/acel.12479 · Cited by 182 · see citing works
Self-citationThe Signaling Pathways Involved in Ovarian Follicle Development
Li, L., Shi, X., Shi, Y., & Wang, Z. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.730196 · Cited by 202 · see citing works
FOXO Transcriptional Factors and Long‐Term Living
Murtaza, G., Khan, A. K., Rashid, R., Muneer, S., Hasan, S. M. F., & Chen, J. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3494289 · Cited by 178 · see citing works
Divergent Roles of Inflammation in Skeletal Muscle Recovery From Injury
Howard, E. E., Pasiakos, S. M., Blesso, C. N., Fussell, M. A., & Rodriguez, N. R. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00087 · Cited by 176 · see citing works
Stem 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 178 · see citing works
Mitochondria Define Intestinal Stem Cell Differentiation Downstream of a FOXO/Notch Axis
Ludikhuize, M. C., Meerlo, M., Pagès-Gallego, M., Xanthakis, D., Julià, M. B., Nguyen, N. B., Brombacher, E. C., Liv, N., Maurice, M. M., Paik, J., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.10.005 · Cited by 169 · see citing works
Damodaran, K., Venkatachalapathy, S., Alisafaei, F., Radhakrishnan, A., Jokhun, D. S., Shenoy, V. B., & Shivashankar, G. V. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-04-0256 · Cited by 164 · 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
Xi, H., Langerman, J., Sabri, S., Chien, P., Young, C. S., Younesi, S., Hicks, M. R., Gonzalez, K. M., Fujiwara, W., Marzi, J., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.04.017 · Cited by 156 · see citing works
FoxO maintains a genuine muscle stem-cell quiescent state until geriatric age
García-Prat, L., Perdiguero, E., Alonso-Martín, S., Dell’Orso, S., Ravichandran, S., Brooks, S. R., Juan, A. H., Campanario, S., Jiang, K., Hong, X., et al. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-00593-7 · Cited by 161 · see citing works
Boonsanay, V., Zhang, T., Georgieva, A. M., Sawa Kostin, D., Qi, H., Yuan, X., Zhou, Y., & Braun, T. W. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.11.002 · Cited by 159 · see citing works
Potential energy landscapes identify the information-theoretic nature of the epigenome
Jenkinson, G., Pujadas, E., Goutsias, J. I., & Feinberg, A. P. (2017) · Nature Genetics · doi:10.1038/ng.3811 · Cited by 152 · see citing works
Autophagy regulates satellite cell ability to regenerate normal and dystrophic muscles
Fiacco, E., Castagnetti, F., Bianconi, V., Madaro, L., Bardi, M. D., Nazio, F., D’Amico, A., Bertini, E., Cecconi, F., Puri, P., et al. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.70 · Cited by 147 · see citing works
Niche Cadherins Control the Quiescence-to-Activation Transition in Muscle Stem Cells
Goel, A. J., Rieder, M.-K., Arnold, H.-H., Radice, G. L., & Krauss, R. S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.102 · Cited by 146 · see citing works
Satellite Cells and Skeletal Muscle Regeneration
Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive physiology · doi:10.1002/j.2040-4603.2015.tb00646.x · Cited by 143 · see citing works
Olsson, K., Saini, A. S., Strömberg, A., Alam, S., Lilja, M. R., Rullman, E., & Gustafsson, T. P. (2015) · Endocrinology · doi:10.1210/en.2015-1685 · Cited by 132 · see citing works
Expanding roles for AMPK in skeletal muscle plasticity
Mounier, R., Théret, M., Lantier, L., Foretz, M., & Viollet, B. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.02.009 · Cited by 130 · 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
Wang, Y. X., Dumont, N. A., & Rudnicki, M. A. (2014) · Journal of Cell Science · doi:10.1242/jcs.151209 · Cited by 125 · see citing works
Xu, M., Chen, X., Chen, D., Yu, B., & Huang, Z. (2016) · Oncotarget · doi:10.18632/oncotarget.12891 · Cited by 119 · 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 121 · see citing works
Metabolic regulation of the hallmarks of stem cell biology
Jackson, B. T., & Finley, L. W. S. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.01.003 · Cited by 122 · see citing works
The Notch signaling network in muscle stem cells during development, homeostasis, and disease
Gioftsidi, S., Relaix, F., & Mourikis, P. (2022) · Skeletal Muscle · doi:10.1186/s13395-022-00293-w · Cited by 115 · see citing works
Ten-eleven translocation 2 interacts with forkhead box O3 and regulates adult neurogenesis
Li, X., Yao, B., Chen, L., Kang, Y., Li, Y., Cheng, Y., Li, L., Li, L., Wang, Z., Wang, M., et al. (2017) · Nature Communications · doi:10.1038/ncomms15903 · Cited by 104 · see citing works
Selenoprotein P Promotes the Development of Pulmonary Arterial Hypertension
Kikuchi, N., Satoh, K., Kurosawa, R., Yaoita, N., Al-Mamun, M. E., Siddique, M. A. H., Omura, J., Satoh, T., Nogi, M., Sunamura, S., et al. (2018) · Circulation · doi:10.1161/circulationaha.117.033113 · Cited by 96 · see citing works
Recent advances in understanding the role of FOXO3
Stefanetti, R. J., Voisin, S. A. C., Russell, A. P., & Lamon, S. (2018) · F1000Research · doi:10.12688/f1000research.15258.1 · Cited by 96 · see citing works
Dayanidhi, S., & Lieber, R. L. (2014) · Muscle & Nerve · doi:10.1002/mus.24441 · Cited by 93 · see citing works
Epigenetic regulation of satellite cell fate during skeletal muscle regeneration
Massenet, J., Gardner, E., Chazaud, B., & Dilworth, F. J. (2021) · Skeletal Muscle · doi:10.1186/s13395-020-00259-w · Cited by 93 · see citing works
FOXO3 on the Road to Longevity: Lessons From SNPs and Chromatin Hubs
Sanese, P., Forte, G., Disciglio, V., Grossi, V., & Simone, C. (2019) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2019.06.011 · Cited by 86 · see citing works
Switching roles: the functional plasticity of adult tissue stem cells
Wabik, A., & Jones, P. H. (2015) · The EMBO Journal · doi:10.15252/embj.201490386 · Cited by 81 · see citing works
FOXOs: masters of the equilibrium
Gui, T., & Burgering, B. M. T. (2021) · FEBS Journal · doi:10.1111/febs.16221 · Cited by 83 · see citing works
Muscle Stem Cell Quiescence: Controlling Stemness by Staying Asleep
Ancel, S., Stuelsatz, P., & Feige, J. N. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2021.02.006 · Cited by 76 · see citing works
Contribution of muscle satellite cells to sarcopenia
Huo, F., Liu, Q., & Liu, H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.892749 · Cited by 74 · see citing works
Interaction between epigenetic and metabolism in aging stem cells
Brunet, A., & Rando, T. A. (2017) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.12.009 · Cited by 76 · see citing works
Self-citationNeural Stem Cells and Nutrients: Poised Between Quiescence and Exhaustion
Cavallucci, V., Fidaleo, M., & Pani, G. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.06.007 · Cited by 72 · see citing works
Kim, M. E., Kim, D. H., & Lee, J. S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911877 · Cited by 74 · see citing works
Keep Your Friends Close: Cell–Cell Contact and Skeletal MyogenesisPreprint
Krauss, R. S., Joseph, G. A., & Goel, A. J. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a029298 · Cited by 68 · see citing works
Regulation of Muscle Growth in Early Postnatal Life in a Swine Model
Rudar, M., Fiorotto, M., & Davis, T. (2018) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-020518-115130 · Cited by 50 · see citing works
Wolfe, A. R., Debeb, B. G., Lacerda, L., Larson, R. A., Bambhroliya, A. B., Huang, X., Bertucci, F., Finetti, P., Birnbaum, D., Laere, S. V., et al. (2015) · Breast Cancer Research and Treatment · doi:10.1007/s10549-015-3645-3 · Cited by 62 · see citing works
Asymmetric Distribution of Primary Cilia Allocates Satellite Cells for Self-Renewal
Marican, N. H. J., Cruz-Migoni, S. B., & Borycki, A. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.04.004 · Cited by 62 · see citing works
Muscle Satellite Cells: Exploring the Basic Biology to Rule Them
de Almeida, C., Fernandes, S., Ribeiro, A. F., Okamoto, O. K., & Vainzof, M. (2016) · Stem Cells International · doi:10.1155/2016/1078686 · Cited by 62 · see citing works
Satellite cell contribution to disease pathology in Duchenne muscular dystrophy
Kodippili, K., & Rudnicki, M. A. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1180980 · Cited by 61 · see citing works
Swahn, H., Mertens, J., Olmer, M., Myers, K., Mondala, T. S., Natarajan, P., Head, S. R., Álvarez-García, Ó., & Lotz, M. (2024) · Advanced Science · doi:10.1002/advs.202309032 · Cited by 61 · see citing works
Hu, L., Liang, S., Chen, H., Lv, T., Wu, J., Chen, D., Wu, M. C., Sun, S., Zhang, H., You, H., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617816114 · Cited by 61 · see citing works
Dzik, K. P., Skrobot, W. R., Kaczor, K. B., Flis, D. J., Karnia, M. J., Libionka, W., Antosiewicz, J., Kloc, W., & Kaczor, J. J. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/6835341 · Cited by 61 · see citing works
ZEB1 protects skeletal muscle from damage and is required for its regeneration
Siles, L., Ninfali, C., Cortés, M., Darling, D. S., & Postigo, A. A. (2019) · Nature Communications · doi:10.1038/s41467-019-08983-8 · Cited by 59 · see citing works
Flamini, V., Ghadiali, R. S., Antczak, P., Rothwell, A., Turnbull, J. E., & Pisconti, A. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.01.007 · Cited by 57 · see citing works
Mycobacterium tuberculosis programs mesenchymal stem cells to establish dormancy and persistence
Fatima, S., Kamble, S. S., Dwivedi, V. P., Bhattacharya, D., Kumar, S., Ranganathan, A., Kaer, L. V., Mohanty, S., & Das, G. (2019) · Journal of Clinical Investigation · doi:10.1172/jci128043 · Cited by 57 · see citing works
Khacho, M., & Slack, R. S. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7228 · Cited by 53 · see citing works
Multiscale 3D genome reorganization during skeletal muscle stem cell lineage progression and aging
Zhao, Y. F., Ding, Y., He, L., Zhou, Q., Chen, X., Li, Y., Alfonsi, M. V., Wu, Z., Sun, H., & Wang, H. (2023) · Science Advances · doi:10.1126/sciadv.abo1360 · Cited by 52 · see citing works
The effect of calorie restriction on mouse skeletal muscle is sex, strain and time-dependent
Boldrin, L., Ross, J. A., Whitmore, C. L., Doreste, B., Beaver, C., Eddaoudi, A., Pearce, D. J., & Morgan, J. E. (2017) · Scientific Reports · doi:10.1038/s41598-017-04896-y · Cited by 51 · see citing works
Gellhaus, B., Böker, K. O., Schilling, A. F., & Saul, D. (2023) · Cells · doi:10.3390/cells12242787 · Cited by 51 · see citing works
Synergizing Engineering and Biology to Treat and Model Skeletal Muscle Injury and Disease
Bursac, N., Juhas, M. E., & Rando, T. A. (2015) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071114-040640 · Cited by 49 · see citing works
Self-citationMetabolic Coordination of Pericyte Phenotypes: Therapeutic Implications
Nwadozi, E., Rudnicki, M., & Haas, T. L. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00077 · Cited by 50 · see citing works
Abreu, P., & Kowaltowski, A. J. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12601 · Cited by 49 · see citing works
The role of FOXOs and autophagy in cancer and metastasis—Implications in therapeutic development
Farhan, M., Silva, M., Li, S., Yan, F., Fang, J., Peng, T., Hu, J., Tsao, M., Little, P. J., & Zheng, W. (2020) · Medicinal Research Reviews · doi:10.1002/med.21695 · Cited by 48 · see citing works
Coaxing stem cells for skeletal muscle repair
McCullagh, K. J. A., & Perlingeiro, R. C. R. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.07.007 · Cited by 47 · see citing works
Adding a “Notch” to Cardiovascular Disease Therapeutics: A MicroRNA-Based Approach
Marracino, L., Fortini, F., Bouhamida, E., Camponogara, F., Severi, P., Mazzoni, E., Patergnani, S., D’Aniello, E., Campana, R., Pinton, P., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.695114 · Cited by 48 · see citing works
p110α of PI3K is necessary and sufficient for quiescence exit in adult muscle satellite cells
Wang, G., Zhu, H., Situ, C., Han, L., Yu, Y., Cheung, T. H., Liu, K., & Wu, Z. (2018) · The EMBO Journal · doi:10.15252/embj.201798239 · Cited by 46 · see citing works
Stem Cells Seen Through the FOXO Lens: An Evolving Paradigm
Liang, R. H.-S., & Ghaffari, S. (2018) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.11.006 · Cited by 45 · see citing works
Ludikhuize, M. C., & Colman, M. J. R. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8126 · Cited by 45 · see citing works
Feng, X., Zhang, Q., Li, J., Bie, N., Li, C., Lian, R., Qin, L., Feng, Y., & Wang, C. (2022) · Food & Function · doi:10.1039/d1fo03830c · Cited by 43 · see citing works
Endo, T. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.09.048 · Cited by 42 · see citing works
The forkhead box O3 (FOXO3): a key player in the regulation of ischemia and reperfusion injury
Omorou, M., Huang, Y., Gao, M., Mu, C., Xu, W., Han, Y., & Xu, H. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04755-2 · Cited by 40 · see citing works
Signaling Role of Pericytes in Vascular Health and Tissue Homeostasis
Fazio, A., Neri, I., Koufi, F., Marvi, M. V., Galvani, A., Evangelisti, C., McCubrey, J. A., Cocco, L., Manzoli, L., & Ratti, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126592 · Cited by 39 · see citing works
Transcription factors FOXO in the regulation of homeostatic hematopoiesis
Menon, V., & Ghaffari, S. (2018) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000441 · Cited by 36 · 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
FOXO3 and Exceptional Longevity: Insights From Hydra to Humans
Davy, P. M. C., Allsopp, R., Donlon, T. A., Morris, B. J., Willcox, D. C., & Willcox, B. J. (2018) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.10.001 · Cited by 37 · see citing works
Sestrin family – the stem controlling healthy ageing
Haidurov, A., & Budanov, A. V. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111379 · Cited by 35 · see citing works
TMEM116 is required for lung cancer cell motility and metastasis through PDK1 signaling pathway
Zhang, S., Dai, H., Li, W., Wang, R., Wu, H., Shen, M., Hu, Y., Xie, L., & Xing, Y. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04369-1 · Cited by 35 · 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
Rejuvenating stem cells to restore muscle regeneration in aging
Bengal, E., Perdiguero, E., Serrano, A. L., & Muñoz‐Cánoves, P. (2017) · F1000Research · doi:10.12688/f1000research.9846.1 · Cited by 30 · see citing works
Fukada, S., & Ito, N. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112907 · Cited by 31 · see citing works
Firat, E., & Niedermann, G. (2016) · Oncotarget · doi:10.18632/oncotarget.10702 · Cited by 30 · see citing works
Loss of foxo rescues stem cell aging in Drosophila germ line
Artoni, F., Kreipke, R. E., Palmeira, O., Dixon, C., Goldberg, Z. H., & Ruohola‐Baker, H. (2017) · eLife · doi:10.7554/elife.27842 · Cited by 29 · see citing works
Gopinath, S. D. (2017) · Skeletal Muscle · doi:10.1186/s13395-017-0121-2 · Cited by 27 · see citing works
Self-citationAutophagy induction during stem cell activation plays a key role in salivary gland self-renewal
Orhon, I., Rocchi, C., Villarejo‐Zori, B., Martinez, P. S., Baanstra, M., Brouwer, U., Boya, P., Coppes, R. P., & Reggiori, F. (2021) · Autophagy · doi:10.1080/15548627.2021.1924036 · Cited by 26 · see citing works
Association Analysis ofFOXO3Longevity Variants With Blood Pressure and Essential Hypertension
Morris, B. J., Chen, R., Donlon, T. A., Evans, D. S., Tranah, G. J., Parimi, N., Ehret, G., Newton‐Cheh, C., Seto, T. B., Willcox, D. C., et al. (2015) · American Journal of Hypertension · doi:10.1093/ajh/hpv171 · Cited by 25 · see citing works
Shan, T., Xu, Z., Wu, W.-C., Liu, J., & Wang, Y. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25730 · Cited by 23 · see citing works
Single-cell chromatin accessibility profiling reveals a self-renewing muscle satellite cell state
Okafor, A. E., Lin, X., Situ, C., Wei, X., Xiang, Y., Wei, X., Wu, Z., & Diao, Y. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202211073 · Cited by 22 · see citing works
New mechanisms driving muscle stem cell regenerative decline with aging
Sousa‐Victor, P., García‐Prat, L., & Muñoz‐Cánoves, P. (2018) · The International Journal of Developmental Biology · doi:10.1387/ijdb.180041pm · Cited by 22 · see citing works
Oxidative stress and inflammation: the root causes of aging
Sobhon, P., Savedvanich, G., & Weerakiet, S. (2023) · Exploration of Medicine · doi:10.37349/emed.2023.00129 · Cited by 26 · see citing works
Choi, J. Y., Hwang, C. Y., Lee, B., Lee, S.-M., Bahn, Y. J., Lee, K., Kang, M., Kim, Y. S., Woo, S., Lim, J., et al. (2016) · Aging · doi:10.18632/aging.101039 · Cited by 22 · see citing works
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 · see citing works
- Authors
- Gopinath, S. D., Webb, A. E., Brunet, A., & Rando, T. A.
- Affiliations
- Stanford Medicine (US)
- VA Palo Alto Health Care System (US)
- Corresponding author
- Rando, Thomas A.
- Venue
- Stem Cell Reports
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 2
- Issue
- 4
- Pages
- 414-426
- ISSN
- 2213-6711 (ISSN-L)
- PMC
- PMC3986584
- OpenAlex
- W2038069027
- Cited by
- 212
- References
- 46
- Citations by year
- 2026: 17 · 2025: 9 · 2024: 13 · 2023: 22 · 2022: 21 · 2021: 16 · 2020: 13 · 2019: 15 · 2018: 19 · 2017: 25 · 2016: 18 · 2015: 21 · 2014: 3
- FWCI
- 9.15
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Stem Cell Reports (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- U.S. Department of Veterans Affairs (I01 BX002324, I01RX001222)
- Ellison Medical Foundation
- Glenn Foundation for Medical Research (P01 AG036695, R01 AR062185)
- Oregon Health and Science University
- Fondation pour la Recherche Médicale
- National Institutes of Health (AG023806, AG036695)
- University of Texas MD Anderson Cancer Center
- National Institute on Aging (R37AG023806, P01AG036695)
- National Cancer Institute (T32CA009302)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR062185)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › FOXO transcription factor regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- FOXO3, skeletal muscle stem cells, satellite cells, quiescence, self-renewal, Notch signaling, Notch1, Notch3, muscle regeneration, differentiation, conditional gene deletion
- MeSH terms
- Forkhead Box Protein O3, Animals, Cell Differentiation, Regeneration, RNA, Messenger, Signal Transduction, Gene Expression, Resting Phase, Cell Cycle, Mice, Knockout, Muscle, Skeletal, Satellite Cells, Skeletal Muscle, Cell Proliferation, Mice, PAX7 Transcription Factor, Forkhead Transcription Factors, Receptors, Notch, Adult Stem Cells
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