The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
mTORC1 controls the adaptive transition of quiescent stem cells from G0 to GAlert
Open accessAbstract
A unique property of many adult stem cells is their ability to exist in a non-cycling, quiescent state. Although quiescence serves an essential role in preserving stem cell function until the stem cell is needed in tissue homeostasis or repair, defects in quiescence can lead to an impairment in tissue function. The extent to which stem cells can regulate quiescence is unknown. Here we show that the stem cell quiescent state is composed of two distinct functional phases, G0 and an 'alert' phase we term G(Alert). Stem cells actively and reversibly transition between these phases in response to injury-induced systemic signals. Using genetic mouse models specific to muscle stem cells (or satellite cells), we show that mTORC1 activity is necessary and sufficient for the transition of satellite cells from G0 into G(Alert) and that signalling through the HGF receptor cMet is also necessary. We also identify G0-to-G(Alert) transitions in several populations of quiescent stem cells. Quiescent stem cells that transition into G(Alert) possess enhanced tissue regenerative function. We propose that the transition of quiescent stem cells into G(Alert) functions as an 'alerting' mechanism, an adaptive response that positions stem cells to respond rapidly under conditions of injury and stress, priming them for cell cycle entry.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“inflammatory initiation of a cell cycle–primed Galert state in HSCs and other cells requires activation of mammalian target of rapamycin (Rodgers et al., 2014).”
From PU.1 enforces quiescence and limits hematopoietic stem cell expansion during inflammatory stress (2021) · cites this paper as Rodgers et al., 2014
Experimental — accuracy not yet measuredIn the citing paper
“Likewise, ‘priming’ of activation by systemic signaling factors has been reported to improve regeneration (Rodgers et al., 2014, 2017).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Rodgers et al., 2014
In the citing paper
“Across all clusters, there were no distinct cell-cycle states observed, consistent with reports of the first division occurring ≥24 hours after our 18 h time point (Gilbert et al., 2010; Rodgers et al., 2014) (Fig. S2D).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Rodgers et al., 2014
In the citing paper
“For instance, although we do not observe bistable transcriptional states between the most-quiescent and most-activated cells in our experiments, stable intermediary activation states might exist in vivo (Rodgers et al., 2014).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Rodgers et al., 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Adjusting batch effects in microarray expression data using empirical Bayes methods
Johnson, W. E., Li, C., & Rabinovic, A. (2007) · Biostatistics · doi:10.1093/biostatistics/kxj037 · Cited by 8,658
mTOR Signaling in Growth Control and Disease
Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509
KEGG for integration and interpretation of large-scale molecular data sets
Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., & Tanabe, M. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr988 · Cited by 4,848
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
G 1 Events and Regulation of Cell Proliferation
Pardee, A. B. (1989) · Science · doi:10.1126/science.2683075 · Cited by 2,182
Wilson, A., Laurenti, E., Oser, G., van der Wath, R. C., Blanco-Bose, W., Jaworski, M., Offner, S., Dunant, C. F., Eshkind, L., Bockamp, E., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.048 · Cited by 1,908
Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis
Joe, A. W. B., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A., & Rossi, F. M. V. (2010) · Nature Cell Biology · doi:10.1038/ncb2015 · Cited by 1,690
Rainer Breitling, A., Armengaud, P., Anna Amtmann, A., & Herzyk, P. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.07.055 · Cited by 1,478
Uezumi, A., Fukada, S., Yamamoto, N., Takeda, S., & Tsuchida, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2014 · Cited by 1,315
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 774
Satellite cell activation and retention of muscle regenerative potential after long-term denervation
Wong, A., Garcia, S. M., Tamaki, S. J., Striedinger, K., Barruet, E., Hansen, S. L., Young, D. M., & Pomerantz, J. H. (2020) · Stem Cells · doi:10.1002/stem.3316 · Cited by 27
Application of Microfluidic Systems for Breast Cancer Research
Frankman, Z. D., Jiang, L., Schroeder, J. A., & Zohar, Y. (2022) · Micromachines · doi:10.3390/mi13020152 · Cited by 28
Adrenergic signaling coordinates distant and local responses to amputation in axolotl
Payzin‐Dogru, D., Froitzheim, T., Blair, S. J., Jena, S. G., Singer, H. D., Paoli, J. C., Kim, R. T., Kriukov, E., Wilson, S., Hou, R., et al. (2025) · Cell · doi:10.1016/j.cell.2025.09.025 · Cited by 26
Delivery of RANKL-Binding Peptide OP3-4 Promotes BMP-2–Induced Maxillary Bone Regeneration
Uehara, T., Mise‐Omata, S., Matsui, M., Tabata, Y., Murali, R., Miyashin, M., & Aoki, K. (2016) · Journal of Dental Research · doi:10.1177/0022034516633170 · Cited by 27
Crizotinib targets in glioblastoma stem cells
Junca, A., Villalva, C., Tachon, G., Rivet, P., Cortes, U., Guilloteau, K., Balbous, A., Godet, J., Wager, M., & Karayan, L. (2017) · Cancer Medicine · doi:10.1002/cam4.1167 · Cited by 27
Chen, Z., Bu, N., Qiao, X., Zuo, Z., Shu, Y.-H., Liu, Z., Qian, Z., Chen, J., & Hou, Y. (2018) · Stem Cells · doi:10.1002/stem.2824 · Cited by 27
Cellular and morphological changes with EAA supplementation before and after total knee arthroplasty
Muyskens, J. B., Foote, D. M., Bigot, N. J., Strycker, L. A., Smolkowski, K., Kirkpatrick, T. K., Lantz, B. A., Shah, S. N., Mohler, C. G., Jewett, B. A., et al. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00869.2018 · Cited by 30
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
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 35
Dai, J., Miller, M. A., Everetts, N. J., Xia, W., Li, P., Li, Y., Xu, J.-H., & Yao, G. (2017) · Oncotarget · doi:10.18632/oncotarget.14634 · Cited by 25
Castel, D., Baghdadi, M. B., Mella, S., Gayraud-Morel, B., Marty, V., Cavaillé, J., Antoniewski, C., & Tajbakhsh, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-21991-w · Cited by 26
Fibroblasts in cancer dormancy: foe or friend?
Dai, L., Mao, L., Zhang, W., Tang, Y.-J., Tang, Y., & Liang, X. (2021) · Cancer Cell International · doi:10.1186/s12935-021-01883-2 · Cited by 27
The m6A reader YTHDC1 regulates muscle stem cell proliferation via PI4K–Akt–mTOR signalling
Liu, J., Zuo, H., Wang, Z., Wang, W., Qian, X., Xie, Y.-Y., Peng, D., Xie, Y., Hong, L., You, W., et al. (2023) · Cell Proliferation · doi:10.1111/cpr.13410 · Cited by 25
Deletion of the Imprinted Gene Grb10 Promotes Hematopoietic Stem Cell Self-Renewal and Regeneration
Yan, X., Himburg, H. A., Pohl, K., Quarmyne, M., Tran, E., Zhang, Y., Fang, T., Kan, J., Chao, N. J., Zhao, L., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.10.025 · Cited by 25
Giovanni, C. D., Novellino, E., Chilin, A., Lavecchia, A., & Marzaro, G. (2016) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2016.1234603 · Cited by 25
Loss of Ptpn11 (Shp2) drives satellite cells into quiescence
Griger, J., Schneider, R., Lahmann, I., Schoewel, V., Keller, C., Spuler, S., Nazaré, M., & Birchmeier, C. (2017) · eLife · doi:10.7554/elife.21552 · Cited by 26
An integrative framework for salamander and mouse limb regeneration
Payzin‐Dogru, D., & Whited, J. L. (2018) · The International Journal of Developmental Biology · doi:10.1387/ijdb.180002jw · Cited by 27
Identification of TOR-responsive slow-cycling neoblasts in planarians
Molinaro, A. M., Lindsay‐Mosher, N., & Pearson, B. J. (2021) · EMBO Reports · doi:10.15252/embr.202050292 · Cited by 24
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
Marcon, B. H., Holetz, F., Eastman, G., Origa-Alves, A. C., Amorós, M., de Aguiar, A. M., Rebelatto, C. L. K., Brofman, P. R. S., Sotelo-Silveira, J. R., & Dallagiovanna, B. (2017) · Stem Cell Research · doi:10.1016/j.scr.2017.10.027 · Cited by 26
Correra, R. M., Ollitrault, D., Valente, M., Mazzola, A., Aðalsteinsson, B. Þ., Ferguson‐Smith, A. C., Marazzi, G., & Sassoon, D. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-32941-x · Cited by 25
Quiescence, an individual journey
Sagot, I., & Laporte, D. (2019) · Current Genetics · doi:10.1007/s00294-018-00928-w · Cited by 26
Mattila, J., Viitanen, A., Fabris, G., Strutynska, T. R., Korzelius, J., & Hietakangas, V. (2024) · Science Advances · doi:10.1126/sciadv.adi2671 · Cited by 26
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
The salamander blastema within the broader context of metazoan regeneration
Tajer, B. J., Savage, A. M., & Whited, J. L. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1206157 · Cited by 25
Notch transactivates Rheb to maintain the multipotency of TSC-null cells
Cho, J., Patel, B. B., Bonala, S., Manne, S., Zhou, Y., Vadrevu, S. K., Patel, J., Peronaci, M., Ghouse, S. M., Henske, E. P., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01845-1 · Cited by 24
Mobley, C. B., Hornberger, T. A., Fox, C. D., Healy, J. C., Ferguson, B. S., Lowery, R. P., McNally, R. M., Lockwood, C. M., Stout, J. R., Kavazis, A. N., et al. (2015) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-015-0094-7 · Cited by 23
The atypical CDK activator RingoA/Spy1 regulates exit from quiescence in neural stem cells
Gonzalez, L., Domingo-Muelas, A., Duart-Abadía, P., Nuñez, M., Mikolčević, P., Llonch, E., Cubillos‐Rojas, M., Cánovas, B., Forrow, S., Morante‐Redolat, J. M., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106202 · Cited by 23
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
PINK1 deficiency alters muscle stem cell fate decision and muscle regenerative capacity
Cairns, G., Thumiah-Mootoo, M., Abbasi, M. R., Gourlay, M., Racine, J., Larionov, N., Prola, A., Khacho, M., & Burelle, Y. (2024) · Stem Cell Reports · doi:10.1016/j.stemcr.2024.03.004 · Cited by 23
Activated Muscle Satellite Cells Chase Ghosts
Mourikis, P., & Relaix, F. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.01.008 · 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
Hocaoglu, H., & Sieber, M. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.03.040 · Cited by 26
Estradiol deficiency reduces the satellite cell pool by impairing cell cycle progression
Larson, A. A., Shams, A. S., McMillin, S. L., Sullivan, B. P., Vue, C., Roloff, Z. A., Batchelor, E., Kyba, M., & Lowe, D. A. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00429.2021 · Cited by 23
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
Molecular clocks, satellite cells, and skeletal muscle regeneration
Kahn, R. E., Dayanidhi, S., Lacham‐Kaplan, O., & Hawley, J. A. (2023) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00073.2023 · Cited by 26
Chromatin signaling in muscle stem cells: interpreting the regenerative microenvironment
Brancaccio, A., & Palacios, D. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00036 · Cited by 24
The role of TORC1 in muscle development in Drosophila
Hatfield, I., Harvey, I. C., Yates, E. R., Redd, J. R., Reiter, L. T., & Bridges, D. (2015) · Scientific Reports · doi:10.1038/srep09676 · Cited by 23
Karyopherin Alpha 1 Regulates Satellite Cell Proliferation and Survival by Modulating Nuclear Import
Choo, H. J., Cutler, A. A., Rother, F., Bäder, M., & Pavlath, G. K. (2016) · Stem Cells · doi:10.1002/stem.2467 · Cited by 23
Riddle, E. S., Bender, E. L., & Thalacker‐Mercer, A. E. (2018) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00135.2018 · Cited by 23
High density is a property of slow-cycling and treatment-resistant human glioblastoma cells
Sabelström, H., Quigley, D. A., Fenster, T., Foster, D. J., Fuchshuber, C. A. M., Saxena, S., Yuan, E., Li, N., Paterno, F., Phillips, J. J., et al. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.03.003 · Cited by 23
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 24
Yue, F., Gu, L., Qiu, J., Oprescu, S. N., Beckett, L. M., Ellis, J. M., Donkin, S. S., & Kuang, S. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00397-1 · Cited by 25
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
mRNA Translation Is Dynamically Regulated to Instruct Stem Cell Fate
Wang, R., & Amoyel, M. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.863885 · Cited by 23
Park, S., Gagliardi, M., Swennen, G., Doğan, A., Kim, Y., Park, Y., Park, G., Oh, S., Post, M. J., & Choi, J. (2022) · Biomolecules · doi:10.3390/biom12060838 · Cited by 22
Mouradian, S., Cicciarello, D., Lacoste, N., Risson, V., Berretta, F., Grand, F. L., Rose, N., Simonet, T., Schaeffer, L., & Scionti, I. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae060 · Cited by 22
Joppé, S. E., Hamilton, L. K., Cochard, L. M., Levros, L.-C., Aumont, A., Barnabé‐Heider, F., & Fernandes, K. J. L. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00407 · Cited by 22
Comparative biology of tissue repair, regeneration and aging
Coffman, J. A., Rieger, S., Rogers, A. N., Updike, D. L., & Yin, V. P. (2016) · npj Regenerative Medicine · doi:10.1038/npjregenmed.2016.3 · Cited by 22
Endogenous Stem Cells in Homeostasis and Aging
Lim, J. E., & Son, Y. (2017) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-017-0097-3 · Cited by 21
Cardiomyogenic differentiation is fine-tuned by differential mRNA association with polysomes
Pereira, I. T., Spangenberg, L., Robert, A. W., Amorín, R., Stimamiglio, M. A., Naya, H., & Dallagiovanna, B. (2019) · BMC Genomics · doi:10.1186/s12864-019-5550-3 · Cited by 20
Tissue Engineering and Regenerative Medicine in Basic Research: A Year in Review of 2014
Huang, J., Lin, X., Shi, Y., & Liu, W. (2015) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2014.0626 · Cited by 23
Physiological Interactions between Microglia and Neural Stem Cells in the Adult Subependymal Niche
Sirerol-Piquer, M. S., Belenguer, G., Morante‐Redolat, J. M., Duart-Abadía, P., Pérez‐Villalba, A., & Fariñas, I. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.01.009 · Cited by 23
Asli, N. S., Xaymardan, M., Patrick, R., Farbehi, N., Cornwell, J. A., Forte, E., Waardenberg, A. J., Janbandhu, V. C., Kesteven, S. H., Chandrakanthan, V., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/225979 · Cited by 22
Rahbek, S. K., Farup, J., de Paoli, F. V., & Vissing, K. (2015) · Amino Acids · doi:10.1007/s00726-014-1907-8 · Cited by 21
Jensen, J., Møller, A. B., Just, J., Mose, M., de Paoli, F. V., Billeskov, T. B., Fred, R. G., Pers, T. H., Pedersen, S. B., Petersen, K. K., et al. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00127.2021 · Cited by 21
Quiescence Through the Prism of Evolution
Daignan‐Fornier, B., Laporte, D., & Sagot, I. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.745069 · Cited by 24
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
Muscle stem cells get a new look: Dynamic cellular projections as sensors of the stem cell niche
Krauss, R. S., & Kann, A. P. (2023) · BioEssays · doi:10.1002/bies.202200249 · Cited by 20
He, Y., Heng, Y., Qin, Z., Wei, X., Wu, Z., & Qu, J. Y. (2023) · Science Advances · doi:10.1126/sciadv.adi1891 · Cited by 21
Tissue Engineering and Regenerative Medicine in Applied Research: A Year in Review of 2014
Lin, X., Huang, J., Shi, Y., & Liu, W. (2015) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2015.0004 · Cited by 21
Amitosenescence and Pseudomitosenescence: Putative New Players in the Aging Process
Wengerodt, D., Schmeer, C. W., Witte, O. W., & Kretz, A. (2019) · Cells · doi:10.3390/cells8121546 · Cited by 21
Autophagy in adult stem cell homeostasis, aging, and disease therapy
Zhao, K., Chan, I. T. C., Tse, E. H. Y., Xie, Z., Cheung, T. H., & Zeng, Y. A. (2025) · Cell Regeneration · doi:10.1186/s13619-025-00224-2 · Cited by 25
Sestrins regulate muscle stem cell metabolic homeostasis
Yang, B. A., Castor‐Macias, J. A., Fraczek, P. M., Cornett, A. M., Brown, L. A., Kim, M., Brooks, S. V., Lombaert, I. M. A., Lee, J. H., & Aguilar, C. A. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.07.014 · Cited by 20
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 23
Muscle satellite cells are impaired in type 2 diabetic mice by elevated extracellular adenosine
Han, L., Wang, G., Zhou, S., Situ, C., He, Z., Li, Y., Qiu, Y., Huang, Y., Xu, A., Ong, M. T., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110884 · Cited by 22
Single cell analysis reveals satellite cell heterogeneity for proinflammatory chemokine expression
Andre, A. B., Rees, K. P., O’Connor, S. A., Severson, G. W., Newbern, J. M., Wilson‐Rawls, J., Plaisier, C. L., & Rawls, A. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1084068 · Cited by 22
“Known Unknowns”: Current Questions in Muscle Satellite Cell Biology
Cornelison, D. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.006 · Cited by 20
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
Rodrigues, C. P., & Akhtar, A. (2021) · Science Advances · doi:10.1126/sciadv.abi5987 · Cited by 21
GLUD1 determines murine muscle stem cell fate by controlling mitochondrial glutamate levels
Soro-Arnáiz, I., Fitzgerald, G., Cherkaoui, S., Zhang, J., Gilardoni, P. A., Ghosh, A., Bar‐Nur, O., Masschelein, E., Maechler, P., Zamboni, N., et al. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.07.015 · Cited by 20
Chaker, Z., Makarouni, E., & Doetsch, F. K. (2024) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-120320-040213 · Cited by 21
Reidy, P. T., Fry, C. S., Dickinson, J. M., Drummond, M. J., & Rasmussen, B. B. (2017) · Physiological Reports · doi:10.14814/phy2.13269 · Cited by 18
Nederveen, J. P., Fortino, S. A., Baker, J. M., Snijders, T., Joanisse, S., McGlory, C., McKay, B. R., Kumbhare, D. A., & Parise, G. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01123.2018 · Cited by 21
Beyond “to divide or not to divide”: Kinetics matters in hematopoietic stem cells
Johnson, C., Belluschi, S., & Laurenti, E. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.11.003 · Cited by 18
Dormancy, Quiescence, and Diapause: Savings Accounts for Life
Ozguldez, H. O., & Bulut-Karslıoğlu, A. (2024) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-112122-022528 · Cited by 17
Zhou, D., Shi, Y., Zhang, D., Zuo, J., Zeng, C., Mamtawla, G., Huang, L., Gao, X., Zhang, L., & Wang, X. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103333 · Cited by 18
Byun, W. S., Lee, J., & Baek, J.-H. (2024) · Inflammation and Regeneration · doi:10.1186/s41232-024-00354-1 · Cited by 20
Sommers, O., Tomsine, R. A., & Khacho, M. (2024) · Cells · doi:10.3390/cells13211773 · Cited by 22
Heng, D., Sheng, X., Tian, C., Li, J., Liu, L., Gou, M., & Liu, L. (2021) · Aging Cell · doi:10.1111/acel.13304 · Cited by 18
Sanvee, G. M., Bouitbir, J., & Krähenbühl, S. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114649 · Cited by 18
A 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
Kim, E., Wu, F., Lim, D., Zeuthen, C., Zhang, Y., Allen, J. P., Muraine, L., Trollet, C., Vest, K. E., & Choo, H. J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.875209 · Cited by 18
Chimge, N., Chen, M.-H., Nguyen, C., Zhao, Y., Wu, X., García-González, P. A., Ogana, H. A. N., Hurwitz, S., Teo, J.-L., Chen, X., et al. (2023) · Current Molecular Pharmacology · doi:10.2174/1874467217666230906092236 · Cited by 21
Transcriptional regulation of autophagy in skeletal muscle stem cells
Krishnan, P. D. G., Lee, W. X., Goh, K. Y., Choy, S. M., Turqueza, L. R. R., Lim, Z. H., & Tang, H.-W. (2025) · Disease Models & Mechanisms · doi:10.1242/dmm.052007 · Cited by 21
Wolf, B., Krieg, K., Falk, C. S., Breuhahn, K., Keppeler, H., Biedermann, T., Schmid, E., Warmann, S. W., Fuchs, J., Vetter, S., et al. (2016) · Cancer Research · doi:10.1158/0008-5472.can-15-3453 · Cited by 18
Prospective purification and characterization of Müller glia in the mouse retina regeneration assay
Schäfer, P., & Karl, M. (2017) · Glia · doi:10.1002/glia.23130 · Cited by 18
Min, K., Lawan, A., & Bennett, A. M. (2017) · Skeletal Muscle · doi:10.1186/s13395-017-0137-7 · Cited by 19
Can laboratory model systems instruct human limb regeneration?
Cox, B. D., Yun, M. H., & Poss, K. D. (2019) · Development · doi:10.1242/dev.181016 · Cited by 18
Fang, M. M., Barman, P. K., Thiruppathi, M., Mirza, R. E., McKinney, R. D., Deng, J., Christman, J. W., Du, X., Fukai, T., Ennis, W. J., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800252 · Cited by 18
Perez, A. C., Santos-de-Frutos, K., de la Rosa, S., Herranz-Montoya, I., Perna, C., & Djouder, N. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20212405 · Cited by 17
Quiescence enables unrestricted cell fate in naive embryonic stem cells
Khoa, L. T. P., Yang, W., Shan, M., Zhang, L., Mao, F., Zhou, B. O., Li, Q., Malcore, R. M., Harris, C. E., Zhao, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46121-1 · Cited by 17
Kim, J. H., Lee, H., Choi, H., Kim, J., Chu, I., Leem, S., & Oh, I. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168036 · Cited by 17
Snijders, T., Bell, K. E., Nederveen, J. P., Saddler, N. I., Mazara, N., Kumbhare, D. A., Phillips, S. M., & Parise, G. (2018) · Journal of Nutrition · doi:10.1093/jn/nxy063 · Cited by 17
Adult Muscle Stem Cells: Exploring the Links Between Systemic and Cellular Metabolism
Purohit, G., & Dhawan, J. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00312 · Cited by 19
Hu, Y., Zhu, Y. X., Gerber, S. D., Osland, J. M., Chen, M., Rao, K., Gu, H., & Yuan, R. (2021) · GeroScience · doi:10.1007/s11357-021-00344-y · Cited by 17
Sicco, C. L., Reverberi, D., Villa, F., Pfeffer, U., Quarto, R., Cancedda, R., & Tasso, R. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-018-1056-1 · Cited by 17
Yao, X., Yu, T., Xi, F., Xu, Y., Ma, L., Pan, X., Chen, S., Han, M., Yin, Y., Dai, X., et al. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.12.082 · Cited by 17
Mg 2+ influx mediated by TRPM7 triggers the initiation of muscle stem cell activation
Hirano, K., Nakabayashi, C., Sasaki, M., Suzuki, M., Aoyagi, Y., Tanaka, K. Y., Murakami, A., Tsuchiya, M., Umemoto, E., Takabayashi, S., et al. (2025) · Science Advances · doi:10.1126/sciadv.adu0601 · Cited by 17
Pro-myogenic small molecules revealed by a chemical screen on primary muscle stem cells
Buchanan, S. M., Price, F. D., Castiglioni, A., Gee, A. W., Schneider, J., Matyas, M. N., Hayhurst, M., Tabebordbar, M., Wagers, A. J., & Rubin, L. L. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-00248-z · Cited by 16
Metadata
- Authors
- Rodgers, J. T., King, K. Y., Brett, J. O., Cromie, M. J., Charville, G. W., Maguire, K. K., Brunson, C., Mastey, N., Liu, L., Tsai, C.-R., Goodell, M. A., & Rando, T. A.
- Affiliations
- Stanford Medicine (US)
- Baylor College of Medicine (US)
- VA Palo Alto Health Care System (US)
- Corresponding author
- Rando, Thomas A.
- ORCID
- Venue
- Nature
- Published
- 2014-05-25
- Volume
- 510
- Issue
- 7505
- Pages
- 393-396
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4065227
- OpenAlex
- W1964204876
- Cited by
- 776
- References
- 35
- Citations by year
- 2026: 48 · 2025: 51 · 2024: 65 · 2023: 93 · 2022: 71 · 2021: 72 · 2020: 64 · 2019: 63 · 2018: 59 · 2017: 80 · 2016: 43 · 2015: 53 · 2014: 14
- FWCI
- 25.82
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- U.S. Department of Veterans Affairs (I01 BX002324)
- China Scholarship Council
- National Institute on Aging (R37AG023806, K99AG041764, R01AG023806, F30AG035521, R01AG047820, P01AG036695)
- National Heart, Lung, and Blood Institute (K08HL098898)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK092883)
- 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 › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- stem cell quiescence, mTORC1, muscle stem cells, satellite cells, hepatocyte growth factor, tissue regeneration, injury response, cell cycle entry
- MeSH terms
- Mechanistic Target of Rapamycin Complex 1, Animals, Cell Cycle, Cells, Cultured, Gene Expression Regulation, Male, Mice, Inbred C57BL, Regeneration, Resting Phase, Cell Cycle, Muscle, Skeletal, Gene Expression Profiling, Satellite Cells, Skeletal Muscle, Multiprotein Complexes, Mice, TOR Serine-Threonine Kinases
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