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Evidence for Cardiomyocyte Renewal in Humans
Open accessAbstract
It has been difficult to establish whether we are limited to the heart muscle cells we are born with or if cardiomyocytes are generated also later in life. We have taken advantage of the integration of carbon-14, generated by nuclear bomb tests during the Cold War, into DNA to establish the age of cardiomyocytes in humans. We report that cardiomyocytes renew, with a gradual decrease from 1% turning over annually at the age of 25 to 0.45% at the age of 75. Fewer than 50% of cardiomyocytes are exchanged during a normal life span. The capacity to generate cardiomyocytes in the adult human heart suggests that it may be rational to work toward the development of therapeutic strategies aimed at stimulating this process in cardiac pathologies.
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“Bergmann et al. estimated that between 0.45 and 1% of human cardiomyocytes renew per annum.”
From The Hippo signal transduction network for exercise physiologists (2016) · cites this paper as [14]
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“Furthermore, they showed that by the age of 50, 40% of the cardiomyocytes had emerged after birth (14).”
From The Hippo signal transduction network for exercise physiologists (2016) · cites this paper as [14]
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“During aging the cell turnover rate declines for several highly-mitotic tissues.”
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Cites
Dynamics of fat cell turnover in humans
Spalding, K. L., Arner, E., Westermark, P. O., Bernard, S., Buchholz, B. A., Bergmann, O., Blomqvist, L., Hoffstedt, J., Näslund, E., Britton, T., et al. (2008) · Nature · doi:10.1038/nature06902 · Cited by 2,357
Self-citationEvidence That Human Cardiac Myocytes Divide after Myocardial Infarction
Beltrami, A. P., Urbanek, K., Kajstura, J., Yan, S., Finato, N., Bussani, R., Nadal‐Ginard, B., Silvestri, F., Leri, A., Beltrami, C. A., et al. (2001) · New England Journal of Medicine · doi:10.1056/nejm200106073442303 · Cited by 1,426
Laflamme, M. A., & Murry, C. E. (2005) · Nature Biotechnology · doi:10.1038/nbt1117 · Cited by 967
Cardiac tumours: diagnosis and management
BUTANY, J. W., Nair, V., Naseemuddin, A., Nair, G. M., Catton, C., & Yau, T. (2005) · The Lancet Oncology · doi:10.1016/s1470-2045(05)70093-0 · Cited by 846
Hsieh, P. C. H., Segers, V. F. M., Davis, M. E., MacGillivray, C., Gannon, J., Molkentin, J. D., Robbins, J. M., & Lee, R. T. (2007) · Nature Medicine · doi:10.1038/nm1618 · Cited by 778
Cardiomyopathy of the aging human heart. Myocyte loss and reactive cellular hypertrophy.
Olivetti, G., Melissari, M., Capasso, J. M., & Anversa, P. (1991) · Circulation Research · doi:10.1161/01.res.68.6.1560 · Cited by 774
Retrospective Birth Dating of Cells in Humans
Spalding, K. L., Bhardwaj, R. D., Buchholz, B. A., Druid, H., & Frisén, J. (2005) · Cell · doi:10.1016/j.cell.2005.04.028 · Cited by 649
Self-citationSurvey of Studies Examining Mammalian Cardiomyocyte DNA Synthesis
Soonpaa, M. H., & Field, L. J. (1998) · Circulation Research · doi:10.1161/01.res.83.1.15 · Cited by 558
Stem-cell-based therapy and lessons from the heart
Passier, R. C., Laake, L. W. V., & Mummery, C. L. (2008) · Nature · doi:10.1038/nature07040 · Cited by 528
The Tropospheric 14CO2 Level in Mid-Latitudes of the Northern Hemisphere (1959–2003)
Levin, I., & Kromer, B. (2004) · Radiocarbon · doi:10.1017/s0033822200033130 · Cited by 527
Flagged first, then by citations
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Research works printed but not linked: 2
- V. Brodsky, D. S. Sarkisov, A. M. Arefyeva, N. W. Panova, I. G. Gvasava, Virchows Arch.424, 429 (1994).
- P. Pfitzer, Curr. Top. Pathol.54, 125 (1971).
Cited by
Sorted by citations
Transient Regenerative Potential of the Neonatal Mouse Heart
Porrello, E. R., Mahmoud, A. I., Simpson, E., Hill, J. A., Richardson, J. A., Olson, E. N., & Sadek, H. A. (2011) · Science · doi:10.1126/science.1200708 · Cited by 2,545
Mesenchymal stem cell perspective: cell biology to clinical progress
Pittenger, M. F., Discher, D. E., Péault, B. M., Phinney, D. G., Hare, J. M., & Caplan, A. I. (2019) · npj Regenerative Medicine · doi:10.1038/s41536-019-0083-6 · Cited by 2,008
Dynamics of hippocampal neurogenesis in adult humans
Spalding, K. L., Bergmann, O., Alkass, K., Bernard, S., Salehpour, M., Huttner, H. B., Boström, E., Westerlund, I., Vial, C., Buchholz, B. A., et al. (2013) · Cell · doi:10.1016/j.cell.2013.05.002 · Cited by 1,841
Self-citationMakkar, R., Smith, R. R., Cheng, K., Malliaras, K. G., Thomson, L., Berman, D. S., Czer, L. S. C., Marbán, L., Mendizabal, A. M., Johnston, P. V., et al. (2012) · The Lancet · doi:10.1016/s0140-6736(12)60195-0 · Cited by 1,423
Mammalian heart renewal by pre-existing cardiomyocytes
Senyo, S. E., Steinhauser, M. L., Pizzimenti, C. L., Yang, V. K., Cai, L., Wang, M., Wu, T.-D., Guerquin-Kern, J.-L., Lechene, C. P., & Lee, R. T. (2013) · Nature · doi:10.1038/nature11682 · Cited by 1,343
Laflamme, M. A., & Murry, C. E. (2011) · Nature · doi:10.1038/nature10147 · Cited by 1,272
Dynamics of Cell Generation and Turnover in the Human Heart
Bergmann, O., Zdunek, S., Felker, A., Salehpour, M., Alkass, K., Bernard, S., Sjostrom, S. L., Szewczykowska, M., Jackowska, T., dos Remedios, C. G., et al. (2015) · Cell · doi:10.1016/j.cell.2015.05.026 · Cited by 1,133
Self-citationPrimary contribution to zebrafish heart regeneration by gata4+ cardiomyocytes
Kikuchi, K., Holdway, J. E., Werdich, A. A., Anderson, R. M., Fang, Y., Egnaczyk, G. F., Evans, T., MacRae, C. A., Stainier, D. Y. R., & Poss, K. D. (2010) · Nature · doi:10.1038/nature08804 · Cited by 1,084
Functional screening identifies miRNAs inducing cardiac regeneration
Eulalio, A., Mano, M., Ferro, M. D., Zentilin, L., Sinagra, G., Zacchigna, S., & Giacca, M. (2012) · Nature · doi:10.1038/nature11739 · Cited by 1,029
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
Neurogenesis in the striatum of the adult human brain
Ernst, A., Alkass, K., Bernard, S., Salehpour, M., Perl, S., Tisdale, J., Possnert, G., Druid, H., & Frisén, J. (2014) · Cell · doi:10.1016/j.cell.2014.01.044 · Cited by 937
Self-citationPuente, B. N., Kimura, W., Muralidhar, S. A., Moon, J., Amatruda, J. F., Phelps, K. L., Grinsfelder, D. B., Rothermel, B. A., Chen, R., Garcia, J. A., et al. (2014) · Cell · doi:10.1016/j.cell.2014.03.032 · Cited by 923
Hippo pathway effector Yap promotes cardiac regeneration
Xin, M., Kim, Y., Sutherland, L. B., Murakami, M., Qi, X., McAnally, J., Porrello, E. R., Mahmoud, A. I., Tan, W., Shelton, J. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313192110 · Cited by 895
The two faces of Hippo: targeting the Hippo pathway for regenerative medicine and cancer treatment
Johnson, R. L., & Halder, G. A. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4161 · Cited by 920
Braunwald, E. (2013) · JACC Heart Failure · doi:10.1016/j.jchf.2012.10.002 · Cited by 862
c-kit+ cells minimally contribute cardiomyocytes to the heart
van Berlo, J. H., Kanisicak, O., Maillet, M., Vagnozzi, R. J., Karch, J. M., Lin, S. J., Middleton, R., Marbán, E., & Molkentin, J. D. (2014) · Nature · doi:10.1038/nature13309 · Cited by 794
BARRETT, B. R., Navrátil, P., & Vary, J. P. (2012) · Progress in Particle and Nuclear Physics · doi:10.1016/j.ppnp.2012.10.003 · Cited by 779
Pathological Ventricular Remodeling
Burchfield, J. S., Xie, M., & Hill, J. A. (2013) · Circulation · doi:10.1161/circulationaha.113.001878 · Cited by 805
A Network of Macrophages Supports Mitochondrial Homeostasis in the Heart
Nicolás-Ávila, J. A., Lechuga-Vieco, A. V., Esteban-Martínez, L., Sánchez-Díaz, M., Díaz-García, E., Santiago, D. J., Rubio-Ponce, A., Li, J. L., Balachander, A., Quintana, J. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.031 · Cited by 762
Cardiomyocyte maturation: advances in knowledge and implications for regenerative medicine
Karbassi, E., Fenix, A. M., Marchianò, S., Muraoka, N., Nakamura, K., Yang, X., & Murry, C. E. (2020) · Nature Reviews Cardiology · doi:10.1038/s41569-019-0331-x · Cited by 796
Aging-Associated Cardiovascular Changes and Their Relationship to Heart Failure
Strait, J. B., & Lakatta, E. G. (2011) · Heart Failure Clinics · doi:10.1016/j.hfc.2011.08.011 · Cited by 769
Regulation of neonatal and adult mammalian heart regeneration by the miR-15 family
Porrello, E. R., Mahmoud, A. I., Simpson, E., Johnson, B. A., Grinsfelder, D. B., Canseco, D. C., Mammen, P. P. A., Rothermel, B. A., Olson, E. N., & Sadek, H. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208863110 · Cited by 754
Cardiovascular remodelling in coronary artery disease and heart failure
Heusch, G., Libby, P., Gersh, B. J., Yellon, D. M., Böhm, M., Lopaschuk, G. D., & Opie, L. H. (2014) · The Lancet · doi:10.1016/s0140-6736(14)60107-0 · Cited by 756
Cardiomyocyte proliferation contributes to heart growth in young humans
Mollova, M., Bersell, K. R., Walsh, S., Savla, J. J., Das, L. T., Park, S., Silberstein, L. E., dos Remedios, C. G., Graham, D. A., Colan, S. D., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214608110 · Cited by 744
Self-citationThe pathophysiology of heart failure with preserved ejection fraction
Borlaug, B. A. (2014) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2014.83 · Cited by 726
Kretzschmar, K., & Watt, F. M. (2012) · Cell · doi:10.1016/j.cell.2012.01.002 · Cited by 756
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Frangogiannis, N. G. (2015) · Comprehensive physiology · doi:10.1002/cphy.c150006 · Cited by 775
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Hatzistergos, K. E., Quevedo, H. C., Oskouei, B. N., Hu, Q., Feigenbaum, G. S., Margitich, I. S., Mazhari, R., Boyle, A., Zambrano, J. P., Rodríguez, J. E., et al. (2010) · Circulation Research · doi:10.1161/circresaha.110.222703 · Cited by 719
3D Bioprinting for Tissue and Organ Fabrication
Zhang, Y. S., Yue, K., Aleman, J., Mollazadeh‐Moghaddam, K., Bakht, S. M., Yang, J., Jia, W., Dell’Erba, V., Assawes, P., Shin, S. R., et al. (2016) · Annals of Biomedical Engineering · doi:10.1007/s10439-016-1612-8 · Cited by 716
Burridge, P. W., Keller, G., Gold, J. D., & Wu, J. C. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2011.12.013 · Cited by 670
Growth of engineered human myocardium with mechanical loading and vascular coculture
Tulloch, N. L., Muskheli, V., Razumova, M. V., Korte, F. S., Regnier, M., Hauch, K. D., Pabon, L., Reinecke, H., & Murry, C. E. (2011) · Circulation Research · doi:10.1161/circresaha.110.237206 · Cited by 666
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Folmes, C. D. L., Dzeja, P. P., Nelson, T. J., & Terzic, A. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.10.002 · Cited by 689
D’Uva, G., Aharonov, A., Lauriola, M., Kain, D., Yahalom-Ronen, Y., Carvalho, S., Weisinger, K., Bassat, E., Rajchman, D., Yifa, O., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3149 · Cited by 667
The extracellular matrix protein agrin promotes heart regeneration in mice
Bassat, E., Mutlak, Y. E., Genzelinakh, A., Shadrin, I. Y., Umansky, K. B., Yifa, O., Kain, D., Rajchman, D., Leach, J. P., Riabov-Bassat, D., et al. (2017) · Nature · doi:10.1038/nature22978 · Cited by 649
Lopaschuk, G. D., & Jaswal, J. S. (2010) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e3181e74a14 · Cited by 636
Role of innate and adaptive immune mechanisms in cardiac injury and repair
Epelman, S., Liu, P. P., & Mann, D. L. (2015) · Nature reviews. Immunology · doi:10.1038/nri3800 · Cited by 663
Liu, Y.-W., Chen, B., Yang, X., Fugate, J. A., Kalucki, F. A., Futakuchi-Tsuchida, A., Couture, L. A., Vogel, K. W., Astley, C. A., Baldessari, A. E., et al. (2018) · Nature Biotechnology · doi:10.1038/nbt.4162 · Cited by 615
The origin of fibroblasts and mechanism of cardiac fibrosis
Krenning, G., Zeisberg, E. M., & Kalluri, R. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22322 · Cited by 601
Meis1 regulates postnatal cardiomyocyte cell cycle arrest
Mahmoud, A. I., Kocabaş, F., Muralidhar, S. A., Kimura, W., Koura, A. S., Thet, S., Porrello, E. R., & Sadek, H. A. (2013) · Nature · doi:10.1038/nature12054 · Cited by 565
Understanding cancer stem cell heterogeneity and plasticity
Tang, D. G. (2012) · Cell Research · doi:10.1038/cr.2012.13 · Cited by 572
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Yeung, M. S. Y., Zdunek, S., Bergmann, O., Bernard, S., Salehpour, M., Alkass, K., Perl, S., Tisdale, J., Possnert, G., Brundin, L., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.011 · Cited by 541
Self-citationMolecular basis of physiological heart growth: fundamental concepts and new players
Maillet, M., van Berlo, J. H., & Molkentin, J. D. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3495 · Cited by 536
The extracellular matrix in myocardial injury, repair, and remodeling
Frangogiannis, N. G. (2017) · Journal of Clinical Investigation · doi:10.1172/jci87491 · Cited by 554
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Sahoo, S., & Losordo, D. W. (2014) · Circulation Research · doi:10.1161/circresaha.114.300639 · Cited by 532
Ellison, G. M., Vicinanza, C., Smith, A. J., Aquila, I., Leone, A., Waring, C. D., Henning, B. J., Stirparo, G. G., Papait, R., Scarfò, M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.07.039 · Cited by 515
Mending broken hearts: cardiac development as a basis for adult heart regeneration and repair
Xin, M., Olson, E. N., & Bassel-Duby, R. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3619 · Cited by 514
Cardiopoietic Stem Cell Therapy in Heart Failure
Bartúnek, J., Behfar, A., Dolatabadi, D., Vanderheyden, M., Ostojić, M., Dens, J., Nakadi, B. E., Banovic, M. D., Beleslin, B., Vrolix, M., et al. (2013) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2013.02.071 · Cited by 504
Additive Manufacturing of Biomaterials, Tissues, and Organs
ZADPOOR, A. A., & Malda, J. (2016) · Annals of Biomedical Engineering · doi:10.1007/s10439-016-1719-y · Cited by 487
Extensive scar formation and regression during heart regeneration after cryoinjury in zebrafish
González‐Rosa, J. M., Martín, V., Peralta, M., Torres, M., & Mercader, N. (2011) · Development · doi:10.1242/dev.060897 · Cited by 463
Hippo signaling impedes adult heart regeneration
Heallen, T., Morikawa, Y., Leach, J., Tao, G., Willerson, J. T., Johnson, R. L., & Martin, J. F. (2013) · Development · doi:10.1242/dev.102798 · Cited by 458
Aging and Autophagy in the Heart
Shirakabe, A., Ikeda, Y., Sciarretta, S., Zablocki, D., & Sadoshima, J. (2016) · Circulation Research · doi:10.1161/circresaha.116.307474 · Cited by 448
Programmed cell death in aging
Tower, J. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.04.002 · Cited by 426
Hirt, M. N., Hansen, A., & Eschenhagen, T. (2014) · Circulation Research · doi:10.1161/circresaha.114.300522 · Cited by 427
Bøtker, H. E., Hausenloy, D. J., Andreadou, I., Antonucci, S., Boengler, K., Davidson, S. M., Deshwal, S., Devaux, Y., Lisa, F. D., Sante, M. D., et al. (2018) · Basic Research in Cardiology · doi:10.1007/s00395-018-0696-8 · Cited by 436
Therapeutic approaches for cardiac regeneration and repair
Hashimoto, H., Olson, E. N., & Bassel‐Duby, R. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0036-6 · Cited by 428
C/EBPβ Controls Exercise-Induced Cardiac Growth and Protects against Pathological Cardiac Remodeling
Boström, P., Mann, N., Wu, J., Quintero, P. A., Plovie, E. R., Panáková, D., Gupta, R. K., Xiao, C., MacRae, C. A., Rosenzweig, A., et al. (2010) · Cell · doi:10.1016/j.cell.2010.11.036 · Cited by 411
Eschenhagen, T., Force, T. L., Ewer, M. S., Keulenaer, G. W. D., Suter, T. M., Anker, S. D., Avkiran, M., de Azambuja, E., Balligand, J., Brutsaert, D. L., et al. (2010) · European Journal of Heart Failure · doi:10.1093/eurjhf/hfq213 · Cited by 410
Targeting regenerative exosomes to myocardial infarction using cardiac homing peptide
Vandergriff, A. C., Huang, K., Shen, D., Hu, S., Hensley, M. T., Caranasos, T. G., Li, Q., & Cheng, K. (2018) · Theranostics · doi:10.7150/thno.20524 · Cited by 413
Dynamics of human adipose lipid turnover in health and metabolic disease
Arner, P., Bernard, S., Salehpour, M., Possnert, G., Liebl, J., Steier, P., Buchholz, B. A., Eriksson, M., Arner, E., Hauner, H., et al. (2011) · Nature · doi:10.1038/nature10426 · Cited by 415
Self-citationCardiomyocyte Regeneration: A Consensus Statement.
Eschenhagen, T., Bolli, R., Braun, T. W., Field, L. J., Fleischmann, B. K., Frisén, J., Giacca, M., Hare, J. M., Houser, S. R., Lee, R. T., et al. (2017) · PubMed · doi:10.1161/circulationaha.117.029343 · Cited by 397
Liu, X., Xiao, J., Zhu, H., Wei, X., Platt, C., Damilano, F., Xiao, C., Bezzerides, V. J., Boström, P., Che, L., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.02.014 · Cited by 397
Mitochondrial quality control mechanisms as molecular targets in cardiac ageing
Picca, A., Mankowski, R. T., Burman, J. L., Donisi, L., Js, K., Marzetti, E., & Leeuwenburgh, C. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0059-z · Cited by 399
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Chong, J. J. H., Chandrakanthan, V., Xaymardan, M., Asli, N. S., Li, J., Ahmed, I. M., Heffernan, C., Menon, M. K., Scarlett, C. J., Rashidianfar, A., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.10.002 · Cited by 386
The Hippo pathway in the heart: pivotal roles in development, disease, and regeneration
Wang, J., Liu, S., Heallen, T. R., & Martin, J. F. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0063-3 · Cited by 389
Loffredo, F. S., Steinhauser, M. L., Gannon, J., & Lee, R. T. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.02.002 · Cited by 386
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White, H. D. (2011) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2011.01.029 · Cited by 378
Dynamics of oligodendrocyte generation in multiple sclerosis
Yeung, M. S. Y., Djelloul, M., Steiner, E., Bernard, S., Salehpour, M., Possnert, G., Brundin, L., & Frisén, J. (2019) · Nature · doi:10.1038/s41586-018-0842-3 · Cited by 376
Self-citationThe Age of Olfactory Bulb Neurons in Humans
Bergmann, O., Liebl, J., Bernard, S., Alkass, K., Yeung, M. S. Y., Steier, P., Kutschera, W., Johnson, L., Landén, M., Druid, H., et al. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.030 · Cited by 409
Self-citationThe roles of senescence and telomere shortening in cardiovascular disease
Fyhrquist, F., Saijonmaa, O. J., & Strandberg, T. E. (2013) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2013.30 · Cited by 373
Force, T. L., & Kolaja, K. L. (2011) · Nature Reviews Drug Discovery · doi:10.1038/nrd3252 · Cited by 370
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Garbern, J. C., & Lee, R. T. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.05.008 · Cited by 376
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Robertson, C., Tran, D., & George, S. C. (2013) · Stem Cells · doi:10.1002/stem.1331 · Cited by 371
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Pagliari, F., Mandoli, C., Forte, G., Magnani, E., Pagliari, S., Nardone, G., Licoccia, S., Minieri, M., Nardo, P. D., & Traversa, E. (2012) · ACS Nano · doi:10.1021/nn2048069 · Cited by 354
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Vlaminck, I. D., Martin, L., Kertesz, M., Patel, K., Kowarsky, M., Strehl, C., Cohen, G., Luikart, H. I., Neff, N. F., Okamoto, J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517494112 · Cited by 357
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Tzahor, E., & Poss, K. D. (2017) · Science · doi:10.1126/science.aam5894 · Cited by 357
Functional Recovery of a Human Neonatal Heart After Severe Myocardial Infarction
Haubner, B. J., Schneider, J., Schweigmann, U., Schuetz, T., Dichtl, W., Velik‐Salchner, C., Stein, J.-I., & Penninger, J. M. (2015) · Circulation Research · doi:10.1161/circresaha.115.307017 · Cited by 355
Cardiac Aging: From Molecular Mechanisms to Significance in Human Health and Disease
Dai, D.-F., Chen, T., Johnson, S. C., Szeto, H., & Rabinovitch, P. S. (2012) · Antioxidants & Redox Signaling · doi:10.1089/ars.2011.4179 · Cited by 334
The Role of Oxidative Stress in Myocardial Ischemia and Reperfusion Injury and Remodeling: Revisited
Kurian, G. A., Rajagopal, R., Vedantham, S., & Rajesh, M. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/1656450 · Cited by 343
Novel therapeutic strategies targeting fibroblasts and fibrosis in heart disease
Gourdie, R. G., Dimmeler, S., & Kohl, P. K. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.89 · Cited by 335
Circadian Rhythm Connections to Oxidative Stress: Implications for Human Health
Wilking, M. J., Ndiaye, M. A., Mukhtar, H., & Ahmad, N. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4889 · Cited by 333
Electrospun conductive nanofibrous scaffolds for engineering cardiac tissue and 3D bioactuators
Wang, L., Wu, Y., Hu, T., Guo, B., & Ma, P. X. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.06.036 · Cited by 321
Dynamic DNA methylation orchestrates cardiomyocyte development, maturation and disease
Gilsbach, R., Preißl, S., Grüning, B. A., Schnick, T., Burger, L., Beneš, V., Würch, A., Bönisch, U., Günther, S., Backofen, R., et al. (2014) · Nature Communications · doi:10.1038/ncomms6288 · Cited by 328
Aged-senescent cells contribute to impaired heart regeneration
Lewis‐McDougall, F. C., Ruchaya, P. J., Domenjo‐Vila, E., Shin Teoh, T., Prata, L., Cottle, B. J., Clark, J. E., Punjabi, P. P., Awad, W., Torella, D., et al. (2019) · Aging Cell · doi:10.1111/acel.12931 · Cited by 317
Hypoxia fate mapping identifies cycling cardiomyocytes in the adult heart
Kimura, W., Xiao, F., Canseco, D. C., Muralidhar, S. A., Thet, S., Zhang, H. M., Abderrahman, Y., Chen, R., Garcia, J. A., Shelton, J. M., et al. (2015) · Nature · doi:10.1038/nature14582 · Cited by 315
Frequency of mononuclear diploid cardiomyocytes underlies natural variation in heart regeneration
Patterson, M., Barske, L. A., Handel, B. V., Rau, C. D., Gan, P., Sharma, A., Parikh, S. S., Denholtz, M., Huang, Y., Yamaguchi, Y., et al. (2017) · Nature Genetics · doi:10.1038/ng.3929 · Cited by 322
Age-associated changes in cardiovascular structure and function: a fertile milieu for future disease
Fleg, J. L., & Strait, J. (2011) · Heart Failure Reviews · doi:10.1007/s10741-011-9270-2 · Cited by 314
Cahill, T. J., Choudhury, R. P., & Riley, P. R. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.106 · Cited by 315
Cardiomyogenesis in the Adult Human Heart
Kajstura, J., Urbanek, K., Perl, S., Hosoda, T., Zheng, H., Ogórek, B., Ferreira‐Martins, J., Goichberg, P., Rondon-Clavo, C., Sanada, F., et al. (2010) · Circulation Research · doi:10.1161/circresaha.110.223024 · Cited by 306
RetractedValidation of the Cardiosphere Method to Culture Cardiac Progenitor Cells from Myocardial Tissue
Davis, D. R., Zhang, Y., Smith, R. R., Cheng, K., Terrovitis, J., Malliaras, K., Li, T.-S., White, A., Makkar, R., & Marbán, E. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007195 · Cited by 300
Regulation of cell proliferation by hypoxia-inducible factors
Hubbi, M. E., & Semenza, G. L. (2015) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00279.2015 · Cited by 311
Mechanisms of Cardiac Regeneration
Uygur, A., & Lee, R. T. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.01.018 · Cited by 304
Cell therapy for cardiac repair—lessons from clinical trials
Behfar, A., Crespo‐Diaz, R. J., Terzic, A., & Gersh, B. J. (2014) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2014.9 · Cited by 298
Cardiac Regenerative Capacity and Mechanisms
Kikuchi, K., & Poss, K. D. (2012) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101011-155739 · Cited by 305
Walsh, S., Pontén, A., Fleischmann, B. K., & Jovinge, S. V. (2010) · Cardiovascular Research · doi:10.1093/cvr/cvq005 · Cited by 290
Self-citationMyocyte Turnover in the Aging Human Heart
Kajstura, J., Gurusamy, N., Ogórek, B., Goichberg, P., Clavo-Rondon, C., Hosoda, T., D'Amario, D., Bardelli, S., Beltrami, A. P., Cesselli, D., et al. (2010) · Circulation Research · doi:10.1161/circresaha.110.231498 · Cited by 287
Self-citationRetractedInfluence of Physical Activity on Hypertension and Cardiac Structure and Function
Hegde, S. M., & Solomon, S. D. (2015) · Current Hypertension Reports · doi:10.1007/s11906-015-0588-3 · Cited by 305
Malliaras, K. G., Zhang, Y., Seinfeld, J., Galang, G., Tseliou, E., Cheng, K., Sun, B., Aminzadeh, M. A., & Marbán, E. (2012) · EMBO Molecular Medicine · doi:10.1002/emmm.201201737 · Cited by 293
Hallmarks of cardiovascular ageing
Abdellatif, M., Rainer, P. P., Sedej, S., & Kroemer, G. (2023) · Nature Reviews Cardiology · doi:10.1038/s41569-023-00881-3 · Cited by 305
Protein homeostasis: live long, won't prosper
Toyama, B. H., & Hetzer, M. W. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3496 · Cited by 283
Metadata
- Authors
- Bergmann, O., Bhardwaj, R. D., Bernard, S., Zdunek, S., Barnabé-Heider, F., Walsh, S., Zupicich, J., Alkass, K., Buchholz, B. A., Druid, H., Jovinge, S., & Frisén, J.
- Affiliations
- Lyon 1 Université (FR)
- Department of Cell and Molecular Biology, Karolinska Institutet, SE-171 77 Stockholm, Sweden.
- Corresponding author
- Bergmann, Olaf
- Bhardwaj, Ratan D.
- Venue
- Science
- Published
- 2009-04-03
- Volume
- 324
- Issue
- 5923
- Pages
- 98-102
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC2991140
- OpenAlex
- W2101986300
- Cited by
- 3,130
- References
- 29
- Citations by year
- 2026: 85 · 2025: 128 · 2024: 150 · 2023: 145 · 2022: 193 · 2021: 204 · 2020: 178 · 2019: 184 · 2018: 185 · 2017: 224 · 2016: 209 · 2015: 222 · 2014: 232 · 2013: 207 · 2012: 211
- FWCI
- 77.38
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- Lund University Publications (Lund University) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (P41GM103483)
- National Center for Research Resources (RR13461, P41RR013461)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- cardiomyocyte renewal, cardiomyocyte turnover, cellular aging, bomb carbon-14, human heart, cardiac regeneration, cardiac pathology
- MeSH terms
- Adult, Aged, Aging, Carbon Radioisotopes, Cell Count, Cell Nucleus, Cell Separation, DNA, Humans, Middle Aged, Models, Cardiovascular, Polyploidy, Stem Cells, Echocardiography, Doppler, Color, Troponin I, Troponin T, Myocytes, Cardiac, Cell Nucleus Division, Cell Proliferation, Nuclear Weapons, Radiometric Dating
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