The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.
Zebrafish heart regeneration occurs by cardiomyocyte dedifferentiation and proliferation
Open accessAbstract
Although mammalian hearts show almost no ability to regenerate, there is a growing initiative to determine whether existing cardiomyocytes or progenitor cells can be coaxed into eliciting a regenerative response. In contrast to mammals, several non-mammalian vertebrate species are able to regenerate their hearts, including the zebrafish, which can fully regenerate its heart after amputation of up to 20% of the ventricle. To address directly the source of newly formed cardiomyocytes during zebrafish heart regeneration, we first established a genetic strategy to trace the lineage of cardiomyocytes in the adult fish, on the basis of the Cre/lox system widely used in the mouse. Here we use this system to show that regenerated heart muscle cells are derived from the proliferation of differentiated cardiomyocytes. Furthermore, we show that proliferating cardiomyocytes undergo limited dedifferentiation characterized by the disassembly of their sarcomeric structure, detachment from one another and the expression of regulators of cell-cycle progression. Specifically, we show that the gene product of polo-like kinase 1 (plk1) is an essential component of cardiomyocyte proliferation during heart regeneration. Our data provide the first direct evidence for the source of proliferating cardiomyocytes during zebrafish heart regeneration and indicate that stem or progenitor cells are not significantly involved in this process.
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?
In the citing paper
“Injury is a well-established trigger of cellular de-differentiation, and the changes we observed are likely a consequence of human neurons adhering to this principle (Gu et al., 2020; Jopling et al., 2010; Poplawski et al., 2020; Renthal et al., 2020; Tzahor and Poss, 2017; Wagner et al., 2017).”
From Age-dependent instability of mature neuronal fate in induced neurons from Alzheimer’s patients (2021) · cites this paper as Jopling et al., 2010
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
Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation
Dor, Y., Brown, J., Martinez, O. I., & Melton, D. A. (2004) · Nature · doi:10.1038/nature02520 · Cited by 2,219
Heart Regeneration in Zebrafish
Poss, K. D., Wilson, L. G., & Keating, M. T. (2002) · Science · doi:10.1126/science.1077857 · Cited by 1,938
The Tol2kit: A multisite gateway‐based construction kit for Tol2 transposon transgenesis constructs
Kwan, K. M., Fujimoto, E., Grabher, C., Mangum, B. D., Hardy, M., Campbell, D. S., Parant, J. M., Yost, H. J., Kanki, J. P., & Chien, C.-B. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21343 · Cited by 1,768
Neuregulin1/ErbB4 Signaling Induces Cardiomyocyte Proliferation and Repair of Heart Injury
Bersell, K. R., Arab, S., Haring, B., & Kühn, B. (2009) · Cell · doi:10.1016/j.cell.2009.04.060 · Cited by 1,053
Practical Methods in Electron Microscopy
Corliss, J. O., & Glauert, A. M. (1973) · Transactions of the American Microscopical Society · doi:10.2307/3224938 · Cited by 1,012
Lepilina, A., Coon, A. N., Kikuchi, K., Holdway, J. E., Roberts, R. W., Burns, C. G., & Poss, K. D. (2006) · Cell · doi:10.1016/j.cell.2006.08.052 · Cited by 848
Controlled expression of transgenes introduced by in vivo electroporation
Matsuda, T., & Cepko, C. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610155104 · Cited by 666
p38 MAP kinase inhibition enables proliferation of adult mammalian cardiomyocytesPreprint
Engel, F. B., Schebesta, M., Duong, M. T., Lü, G., Ren, S. V., Madwed, J. B., Jiang, H., Wang, Y., & Keating, M. T. (2005) · Genes & Development · doi:10.1101/gad.1306705 · Cited by 595
Conditional targeted cell ablation in zebrafish: A new tool for regeneration studies
Curado, S., Anderson, R. M., Jungblut, B., Mumm, J. S., Schroeter, E. H., & Stainier, D. Y. R. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21100 · Cited by 509
Huang, C., Tu, C., Hsiao, C., Hsieh, F., & Tsai, H. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10356 · Cited by 506
Cited by
Sorted by citations
Items 101–200 of 1,000
Regulation of zebrafish heart regeneration by miR-133
Yin, V. P., Lepilina, A., Smith, A., & Poss, K. D. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.02.018 · Cited by 195
Singh, A., Singh, A., & Sen, D. (2016) · Stem Cell Research & Therapy · doi:10.1186/s13287-016-0341-0 · Cited by 203
Choi, W.-Y., Gemberling, M. P., Wang, J., Holdway, J. E., Shen, M., Karlstrom, R. O., & Poss, K. D. (2013) · Development · doi:10.1242/dev.088526 · Cited by 195
Nkx2.2 repressor complex regulates islet β-cell specification and prevents β-to-α-cell reprogrammingPreprint
Papizan, J. B., Singer, R. A., Tschen, S.-I., Dhawan, S., Friel, J. M., Hipkens, S. B., Magnuson, M. A., Bhushan, A., & Sussel, L. (2011) · Genes & Development · doi:10.1101/gad.173039.111 · Cited by 193
Fang, Y., Gupta, V., Karra, R., Holdway, J. E., Kikuchi, K., & Poss, K. D. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1309810110 · Cited by 190
Derks, W. J. A., & Bergmann, O. (2020) · Circulation Research · doi:10.1161/circresaha.119.315408 · Cited by 197
Wu, C. C., Kruse, F., Vasudevarao, M. D., Junker, J. P., Zebrowski, D. C., Fischer, K. J., Noël, E. S., Grün, D., Berezikov, E., Engel, F. B., et al. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.12.010 · Cited by 192
Soufi, A., & Dalton, S. (2016) · Development · doi:10.1242/dev.142075 · Cited by 190
Zebrafish heart regeneration: 15 years of discoveries
González‐Rosa, J. M., Burns, C. E., & Burns, C. G. (2017) · Regeneration · doi:10.1002/reg2.83 · Cited by 193
A genetically targetable near-infrared photosensitizer
He, J., Wang, Y., Missinato, M. A., Onuoha, E. O., Perkins, L. A., Watkins, S. C., Croix, C. M. S., Tsang, M., & Bruchez, M. P. (2016) · Nature Methods · doi:10.1038/nmeth.3735 · Cited by 180
Ponnusamy, M., Liu, F., Zhang, Y., Li, R.-B., Zhai, M., Liu, F., Zhou, L.-Y., Liu, C.-Y., Yan, K.-W., Dong, Y., et al. (2019) · Circulation · doi:10.1161/circulationaha.118.035832 · Cited by 181
Traxler, L., Herdy, J. R., Stefanoni, D., Eichhorner, S., Pelucchi, S., Szücs, A., Santagostino, A., Kim, Y., Agarwal, R. K., Schlachetzki, J. C. M., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.07.014 · Cited by 179
Mechanisms of Cardiac Repair and Regeneration
Broughton, K. M., Wang, B. J., Firouzi, F., Khalafalla, F. G., Dimmeler, S., Fernández‐Avilés, F., & Sussman, M. A. (2018) · Circulation Research · doi:10.1161/circresaha.117.312586 · Cited by 182
Surgical models for cardiac regeneration in neonatal mice
Mahmoud, A. I., Porrello, E. R., Kimura, W., Olson, E. N., & Sadek, H. A. (2014) · Nature Protocols · doi:10.1038/nprot.2014.021 · Cited by 180
Cardiac muscle regeneration: lessons from developmentPreprint
Mercola, M. A., Ruiz‐Lozano, P., & Schneider, M. D. (2011) · Genes & Development · doi:10.1101/gad.2018411 · Cited by 176
Sdek, P., Zhao, P., Wang, Y., Huang, C.-J., Ko, C. Y., Butler, P. C., Weiss, J. N., & MacLellan, W. R. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201012049 · Cited by 177
Polyploidy in tissue homeostasis and regeneration
Øvrebø, J. I., & Edgar, B. A. (2018) · Development · doi:10.1242/dev.156034 · Cited by 171
The local microenvironment limits the regenerative potential of the mouse neonatal heart
Notari, M., Ventura-Rubio, A., Bedford-Guaus, S. J., Jorba, I., Mulero, L., Navajas, D., Martí, M., & Raya, Á. (2018) · Science Advances · doi:10.1126/sciadv.aao5553 · Cited by 171
Self-citationHypoxia Induces Myocardial Regeneration in Zebrafish
Jopling, C., Suñé, G., Faucherre, A., Fabregat, C., & Belmonte, J. C. I. (2012) · Circulation · doi:10.1161/circulationaha.112.107888 · Cited by 168
Self-citationDevelopment of the cerebellum and cerebellar neural circuits
Hibi, M., & Shimizu, T. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20875 · Cited by 166
A neonatal blueprint for cardiac regeneration
Porrello, E. R., & Olson, E. N. (2014) · Stem Cell Research · doi:10.1016/j.scr.2014.06.003 · Cited by 177
Cardiomyocyte—Endothelial Cell Interactions in Cardiac Remodeling and Regeneration
Talman, V., & Kivelä, R. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00101 · Cited by 179
Bär, C., de Jesus, B. B., Serrano, R., Tejera, A., Ayuso, E., Jimenez, V., Formentini, I., Bobadilla, M., Mizrahi, J., de Martino, A., et al. (2014) · Nature Communications · doi:10.1038/ncomms6863 · Cited by 162
Zebrafish as a model for normal and malignant hematopoiesis
Jing, L., & Zon, L. I. (2011) · Disease Models & Mechanisms · doi:10.1242/dmm.006791 · Cited by 164
Beisaw, A., Kuenne, C. T., Günther, S., Dallmann, J., Wu, C. C., Bentsen, M. S., Looso, M., & Stainier, D. Y. R. (2020) · Circulation Research · doi:10.1161/circresaha.119.316167 · Cited by 166
Cardiomyocyte renewal in the human heart: insights from the fall-out
Lázár, E., Sadek, H. A., & Bergmann, O. (2017) · European Heart Journal · doi:10.1093/eurheartj/ehx343 · Cited by 163
The zebrafish as a tool to identify novel therapies for human cardiovascular disease
Asnani, A. H., & Peterson, R. T. (2014) · Disease Models & Mechanisms · doi:10.1242/dmm.016170 · Cited by 169
Transcriptional Reversion of Cardiac Myocyte Fate During Mammalian Cardiac Regeneration
O'Meara, C. C., Wamstad, J. A., Gladstone, R. A., Fomovsky, G. M., Butty, V. L., Shrikumar, A., Gannon, J., Boyer, L. A., & Lee, R. T. (2014) · Circulation Research · doi:10.1161/circresaha.116.304269 · Cited by 164
Limb Regeneration: A New Development?
Nacu, E., & Tanaka, E. M. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154115 · Cited by 155
Immunomodulatory Functions of Mesenchymal Stem Cells in Tissue Engineering
Li, H., Shen, S. H., Fu, H., Wang, Z., Li, X., Sui, X., Yuan, M., Liu, S., Wang, G., & Guo, Q. (2019) · Stem Cells International · doi:10.1155/2019/9671206 · Cited by 151
MAPK/ERK Pathway as a Central Regulator in Vertebrate Organ Regeneration
Wen, X., Jiao, L., & Tan, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031464 · Cited by 156
Yahalom-Ronen, Y., Rajchman, D., Sarig, R., Geiger, B., & Tzahor, E. (2015) · eLife · doi:10.7554/elife.07455 · Cited by 150
Huang, Y., Harrison, M. R., Osorio, A., Kim, J., Baugh, A., Duan, C., Sucov, H. M., & Lien, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067266 · Cited by 151
Witman, N., Murtuza, B., Davis, B., Arner, A., & Morrison, J. I. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.03.021 · Cited by 151
Signaling During Epicardium and Coronary Vessel Development
Pérez-Pomares, J. M., & de la Pompa, J. L. (2011) · Circulation Research · doi:10.1161/circresaha.111.245589 · Cited by 147
Mercer, S. E., Odelberg, S. J., & Simon, H. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.08.002 · Cited by 144
Ye, L., Zimmermann, W., Garry, D. J., & Zhang, J. J. (2013) · Circulation Research · doi:10.1161/circresaha.113.300216 · Cited by 145
Steinhauser, M. L., & Lee, R. T. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201100175 · Cited by 146
Wang, Z., Cui, M., Shah, A. M., Ye, W., Tan, W. H., Min, Y.-L., Botten, G. A., Shelton, J. M., Liu, N., Bassel‐Duby, R., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905824116 · Cited by 143
González‐Rosa, J. M., Peralta, M., & Mercader, N. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.07.007 · Cited by 145
Lam, N. T., & Sadek, H. A. (2018) · Circulation · doi:10.1161/circulationaha.118.033648 · Cited by 147
Differentiated skeletal cells contribute to blastema formation during zebrafish fin regeneration
Sousa, S. H., Afonso, N., Bensimon‐Brito, A., Fonseca, M., Simões, M. G., Rodríguez‐León, J., Roehl, H. H., Cancela, M. L., & Jacinto, A. (2011) · Development · doi:10.1242/dev.064717 · Cited by 140
Origins of cardiac fibroblasts
Moore-Morris, T., Cattaneo, P., Puceat, M., & Evans, S. M. (2016) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.12.031 · Cited by 139
Zebrowski, D. C., Vergarajauregui, S., Wu, C. C., Piatkowski, T., Becker, R., Leone, M., Hirth, S., Ricciardi, F., Falk, N., Gießl, A., et al. (2015) · eLife · doi:10.7554/elife.05563 · Cited by 138
Hydrogen peroxide primes heart regeneration with a derepression mechanism
Han, P., Zhou, X., Chang, N., Xiao, C., Yan, S., Ren, H., Yang, X., Zhang, M., Wu, Q., Tang, B., et al. (2014) · Cell Research · doi:10.1038/cr.2014.108 · Cited by 143
Origin and function of activated fibroblast states during zebrafish heart regeneration
Hu, B., Lelek, S., Spanjaard, B., El‐Sammak, H., Simões, M. G., Mintcheva, J., Aliee, H., Schäfer, R., Meyer, A. M., Theis, F. J., et al. (2022) · Nature Genetics · doi:10.1038/s41588-022-01129-5 · Cited by 140
Migration of cardiomyocytes is essential for heart regeneration in zebrafish
Itou, J., Oishi, I., Kawakami, H., Glass, T. J., Richter, J., Johnson, A., Lund, T. C., & Kawakami, Y. (2012) · Development · doi:10.1242/dev.079756 · Cited by 142
Cardiac regeneration based on mechanisms of cardiomyocyte proliferation and differentiation
Senyo, S. E., Lee, R. T., & Kühn, B. (2014) · Stem Cell Research · doi:10.1016/j.scr.2014.09.003 · Cited by 136
Organ repair and regeneration: An overview
Baddour, J., Sousounis, K., & Tsonis, P. A. (2012) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21006 · Cited by 137
Wadugu, B. A., & Kühn, B. (2012) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00063.2012 · Cited by 135
Chen, J., He, J., Ni, R., Yang, Q., Zhang, Y., & Luo, L. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.03.022 · Cited by 133
Cryoinjury as a myocardial infarction model for the study of cardiac regeneration in the zebrafish
González‐Rosa, J. M., & Mercader, N. (2012) · Nature Protocols · doi:10.1038/nprot.2012.025 · Cited by 131
Galdos, F. X., Guo, Y., Paige, S. L., VanDusen, N. J., Wu, S. M., & Pu, W. T. (2017) · Circulation Research · doi:10.1161/circresaha.116.309040 · Cited by 135
Shapiro, S., Ranjan, A. K., Kawase, Y., Cheng, R. K.-H., Kara, R. J., Bhattacharya, R., Guzmán, G., Sanz, J., Garcia, M. J., & Chaudhry, H. W. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3007668 · Cited by 130
The cell biology of regeneration
King, R. S., & Newmark, P. A. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201105099 · Cited by 137
Structure and function of the Nppa–Nppb cluster locus during heart development and disease
Man, J. C. K., Barnett, P., & Christoffels, V. M. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2737-0 · Cited by 132
Strategies for Cardiac Regeneration and Repair
Lin, Z., & Pu, W. T. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3006681 · Cited by 131
Evolution, comparative biology and ontogeny of vertebrate heart regeneration
Vivien, C. J., Hudson, J. E., & Porrello, E. R. (2016) · npj Regenerative Medicine · doi:10.1038/npjregenmed.2016.12 · Cited by 128
Hand2 elevates cardiomyocyte production during zebrafish heart development and regeneration
Schindler, Y. L., Garske, K. M., Wang, J., Firulli, B. A., Firulli, A. B., Poss, K. D., & Yelon, D. L. (2014) · Development · doi:10.1242/dev.106336 · Cited by 128
Limited dedifferentiation provides replacement tissue during zebrafish fin regeneration
Stewart, S., & Stankunas, K. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.02.031 · Cited by 126
An Injury-Responsive Gata4 Program Shapes the Zebrafish Cardiac Ventricle
Gupta, V., Gemberling, M. P., Karra, R., Rosenfeld, G. E., Evans, T., & Poss, K. D. (2013) · Current Biology · doi:10.1016/j.cub.2013.05.028 · Cited by 127
Zebrafish models of cardiovascular disease
Bournele, D., & Beis, D. (2016) · Heart Failure Reviews · doi:10.1007/s10741-016-9579-y · Cited by 129
Zhao, L., Ben-Yair, R., Burns, C. E., & Burns, C. G. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.048 · Cited by 128
Differential reparative phenotypes between zebrafish and medaka after cardiac injury
Ito, K., Morioka, M., Kimura, S., Tasaki, M., Inohaya, K., & Kudō, A. (2014) · Developmental Dynamics · doi:10.1002/dvdy.24154 · Cited by 128
Wnt/β-catenin signaling in heart regeneration
Özhan, G., & Weidinger, G. (2015) · Cell Regeneration · doi:10.1186/s13619-015-0017-8 · Cited by 125
Development, Proliferation, and Growth of the Mammalian Heart
Günthel, M., Barnett, P., & Christoffels, V. M. (2018) · Molecular Therapy · doi:10.1016/j.ymthe.2018.05.022 · Cited by 129
Noseda, M., Peterkin, T., Simões, F. C., Patient, R. K., & Schneider, M. D. (2011) · Circulation Research · doi:10.1161/circresaha.110.223792 · Cited by 120
Stimulation of glycolysis promotes cardiomyocyte proliferation after injury in adult zebrafish
Fukuda, R., Marín‐Juez, R., El‐Sammak, H., Beisaw, A., Ramadass, R., Kuenne, C. T., Günther, S., Konzer, A., Bhagwat, A. M., Graumann, J., et al. (2020) · EMBO Reports · doi:10.15252/embr.201949752 · Cited by 124
Simon, A., & Tanaka, E. M. (2012) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.73 · Cited by 118
Heart Regeneration in the Mexican Cavefish
Stockdale, W. T., Lemieux, M. E., Killen, A. C., Zhao, J., Hu, Z., Riepsaame, J., Hamilton, N., Kudoh, T., Riley, P. R., van Aerle, R., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.072 · Cited by 119
Formiga, F. R., Pelacho, B., Garbayo, E., Imbuluzqueta, I., Díaz-Herráez, P., Abizanda, G., Gavira, J. J., Simón‐Yarza, T., Albiasu, E., Tamayo, E., et al. (2013) · Journal of Controlled Release · doi:10.1016/j.jconrel.2013.10.034 · Cited by 117
Cardiac Development and Implications for Heart Disease
Epstein, J. A. (2010) · New England Journal of Medicine · doi:10.1056/nejmra1003941 · Cited by 116
Do Neonatal Mouse Hearts Regenerate following Heart Apex Resection?
Andersen, D. C., Ganesalingam, S., Jensen, C. H., & Sheikh, S. P. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.02.008 · Cited by 115
Han, Y., Chen, A., Umansky, K. B., Oonk, K. A., Choi, W.-Y., Dickson, A. L., Ou, J., Cigliola, V., Yifa, O., Cao, J., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.01.001 · Cited by 119
Zebrafish models in cardiac development and congenital heart birth defects
Tu, S., & Chi, N. C. (2012) · Differentiation · doi:10.1016/j.diff.2012.05.005 · Cited by 117
See, K., Tan, W. L. W., Lim, E. H., Tiang, Z., Lee, L. T., Li, P. Y. Q., Luu, T. D. A., Ackers-Johnson, M. A., & Foo, R. (2017) · Nature Communications · doi:10.1038/s41467-017-00319-8 · Cited by 115
Lineage conversion methodologies meet the reprogramming toolbox
Sancho-Martinez, I., Baek, S. H., & Belmonte, J. C. I. (2012) · Nature Cell Biology · doi:10.1038/ncb2567 · Cited by 115
Self-citationMyocardial NF-κB activation is essential for zebrafish heart regeneration
Karra, R., Knecht, A. K., Kikuchi, K., & Poss, K. D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511209112 · Cited by 117
Leone, M., Magadum, A., & Engel, F. B. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00559.2015 · Cited by 115
p53 on the crossroad between regeneration and cancer
Charni‐Natan, M., Aloni-Grinstein, R., Molchadsky, A., & Rotter, V. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.117 · Cited by 115
Regulation of p53 is critical for vertebrate limb regeneration
Yun, M. H., Gates, P. B., & Brockes, J. P. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310519110 · Cited by 116
Identification and characterization
Bernstein, J., & Reutzel‐Edens, S. M. (2019) · urn:isbn:978-1-118-41628-0 · Cited by 112
Paradis, A. N., Gay, M. S., & Zhang, L. (2013) · Drug Discovery Today · doi:10.1016/j.drudis.2013.10.019 · Cited by 118
Heart regeneration: 20 years of progress and renewed optimism
Garbern, J. C., & Lee, R. T. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.01.012 · Cited by 115
In vivo partial cellular reprogramming enhances liver plasticity and regeneration
Hishida, T., Yamamoto, M., Hishida-Nozaki, Y., Shao, C., Huang, L., Wang, C., Shojima, K., Xue, Y., Hang, Y., Shokhirev, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110730 · Cited by 116
Self-citationCardiac regeneration: current therapies-future concepts.
Doppler, S. A., Deutsch, M.-A., Lange, R., & Krane, M. (2013) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2072-1439.2013.08.71 · Cited by 112
A dual epimorphic and compensatory mode of heart regeneration in zebrafish
Sallin, P., Charles, A.-S. D. P., Duruz, V., Pfefferli, C., & Jaźwińska, A. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.12.002 · Cited by 109
Small molecules for reprogramming and transdifferentiation
Qin, H., Zhao, A., & Fu, X. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2586-x · Cited by 109
The transcription factor GATA4 promotes myocardial regeneration in neonatal mice
Mohammadi, M. M., Kattih, B., Grund, A., Froese, N., Korf‐Klingebiel, M., Gigina, A., Schrameck, U., Rudat, C., Liang, Q., Kispert, A., et al. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201606602 · Cited by 113
Münch, J., Grivas, D., González-Rajal, Á., Torregrosa-Carrión, R., & de la Pompa, J. L. (2017) · Development · doi:10.1242/dev.143362 · Cited by 112
Fetal Mammalian Heart Generates a Robust Compensatory Response to Cell Loss
Sturzu, A. C., Rajarajan, K., Passer, D., Plonowska‐Hirschfeld, K. A., Riley, A. K., Tan, T. C., Sharma, A., Xu, A., Engels, M. C., Feistritzer, R., et al. (2015) · Circulation · doi:10.1161/circulationaha.114.011490 · Cited by 110
Cao, J., Navis, A. R., Cox, B. D., Dickson, A. L., Gemberling, M. P., Karra, R., Bagnat, M., & Poss, K. D. (2015) · Development · doi:10.1242/dev.130534 · Cited by 107
Zebrafish Models of Cardiac Disease: From Fortuitous Mutants to Precision Medicine
González‐Rosa, J. M. (2022) · Circulation Research · doi:10.1161/circresaha.122.320396 · Cited by 111
Cardiac Regeneration and Stem Cells
Zhang, Y., Mignone, J., & MacLellan, W. R. (2015) · Physiological Reviews · doi:10.1152/physrev.00021.2014 · Cited by 110
The epicardium signals the way towards heart regeneration
Masters, M., & Riley, P. R. (2014) · Stem Cell Research · doi:10.1016/j.scr.2014.04.007 · Cited by 111
Huang, W., Yang, C., Chen, I.-H., Liu, Y.-M. L., Chang, S., & Chuang, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066613 · Cited by 108
Stage-specific effects of Notch activation during skeletal myogenesis
Bi, P., Yue, F., Sato, Y., Wirbisky, S. E., Liu, W., Shan, T., Wen, Y., Zhou, D., Freeman, J. L., & Kuang, S. (2016) · eLife · doi:10.7554/elife.17355 · Cited by 105
Cai, M.-X., Shi, X.-C., Chen, T., Tan, Z.-N., Lin, Q.-Q., Du, S.-J., & Tian, Z.-J. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.02.055 · Cited by 101
Recent Developments in Heart Failure
Dassanayaka, S., & Jones, S. P. (2015) · Circulation Research · doi:10.1161/circresaha.115.305765 · Cited by 103
The ontogeny, activation and function of the epicardium during heart development and regeneration
Simões, F. C., & Riley, P. R. (2018) · Development · doi:10.1242/dev.155994 · Cited by 101
Metadata
- Authors
- Jopling, C., Sleep, E., Raya, M., Martí, M., Raya, A., & Belmonte, J. C. I.
- Affiliations
- Center of Regenerative Medicine in Barcelona (ES)
- Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES)
- Salk Institute for Biological Studies (US)
- Corresponding author
- Belmonte, Juan Carlos Izpisúa
- Venue
- Nature
- Published
- 2010-03-25
- Volume
- 464
- Issue
- 7288
- Pages
- 606-609
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2846535
- OpenAlex
- W1998457769
- Cited by
- 1,333
- References
- 25
- Citations by year
- 2026: 54 · 2025: 73 · 2024: 53 · 2023: 59 · 2022: 85 · 2021: 104 · 2020: 98 · 2019: 83 · 2018: 99 · 2017: 74 · 2016: 82 · 2015: 88 · 2014: 82 · 2013: 93 · 2012: 101
- FWCI
- 38.85
- 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
- G. Harold and Leila Y. Mathers Foundation
- Ministerio de Ciencia e Innovación
- National Heart, Lung, and Blood Institute (R33HL088293)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- zebrafish heart regeneration, cardiomyocyte dedifferentiation, cardiomyocyte proliferation, myocardial infarction, PLK1, sarcomere disassembly, cell cycle regulators, cardiac progenitor cells
- MeSH terms
- Polo-Like Kinase 1, Animals, Gene Expression Regulation, Heart, Proto-Oncogene Proteins, Regeneration, Sarcomeres, Zebrafish, Protein Serine-Threonine Kinases, Cell Cycle Proteins, Cell Lineage, Myocytes, Cardiac, Cell Proliferation, Cell Dedifferentiation
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