Erratum: Myc overexpression enhances epicardial contribution to the developing heart and promotes extensive expansion of the cardiomyocyte population (Scientific Reports (2016) 6 (35366) DOI: 10.1038/srep35366);Myc overexpression enhances of epicardial contribution to the developing heart and promotes extensive expansion of the cardiomyocyte population

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Villa Del Campo, Cristina ^a   Lioux, Ghislaine ^a   Carmona, Rita ^b,c   Sierra, Rocío ^a   Muñoz Chápuli, Ramón ^b,c   Clavería, Cristina ^a   Torres, Miguel ^a  

^a CENTRO NACIONAL DE INVESTIGACIONES CARDIOVASCULARES CNIC   (Spain)

^b UNIVERSITY OF MÁLAGA   (Spain)

^c Institute of Biomedical Research in Malaga and BIONAND Nanomedicine Platform   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

COMPETITIVE ABILITY; EPICARDIUM; GENE OVEREXPRESSION; HEART CELL CULTURE; HEART DEVELOPMENT; PRECURSOR; VASCULARIZATION; WILD TYPE; ANIMAL; CARDIAC MUSCLE; CARDIAC MUSCLE CELL; CELL DIFFERENTIATION; CELL LINEAGE; CELL PROLIFERATION; CORONARY BLOOD VESSEL; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; HEART; METABOLISM; MOUSE; ORGANOGENESIS; PATHOLOGY; PERICARDIUM;

CRE RECOMBINASE; INTEGRASE; MYC PROTEIN;

ANIMALS; CELL DIFFERENTIATION; CELL LINEAGE; CELL PROLIFERATION; CORONARY VESSELS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HEART; INTEGRASES; MICE; MYOCARDIUM; MYOCYTES, CARDIAC; ORGANOGENESIS; PERICARDIUM; PROTO-ONCOGENE PROTEINS C-MYC;

EID: 84993995112     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep37880     Document Type: Erratum

References (39)

1. Manner, J., Perez-Pomares, J. M., Macias, D. & Munoz-Chapuli, R. The origin, formation and developmental significance of the epicardium: a review. Cells Tissues Organs 169, 89-103 (2001).
2. Schulte, I., Schlueter, J., Abu-Issa, R., Brand, T. & Manner, J. Morphological and molecular left-right asymmetries in the development of the proepicardium: a comparative analysis on mouse and chick embryos. Dev Dyn 236, 684-695, doi: 10.1002/dvdy.21065 (2007).
3. Dettman, R. W., Denetclaw, W. Jr., Ordahl, C. P. & Bristow, J. Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart. Developmental biology 193, 169-181, doi: 10.1006/ dbio.1997.8801 (1998).
4. Perez-Pomares, J. M., Macias, D., Garcia-Garrido, L. & Munoz-Chapuli, R. Contribution of the primitive epicardium to the subepicardial mesenchyme in hamster and chick embryos. Dev Dyn 210, 96-105, doi: 10.1002/(SICI)1097-0177(199710)210:2 3.0.CO;2-4 (1997).
5. 5Vrancken Peeters, M. P., Gittenberger-de Groot, A. C., Mentink, M. M. & Poelmann, R. E. Smooth muscle cells and fibroblasts of the coronary arteries derive from epithelial-mesenchymal transformation of the epicardium. Anatomy and embryology 199, 367-378 (1999).
6. Mikawa, T. & Fischman, D. A. Retroviral analysis of cardiac morphogenesis: discontinuous formation of coronary vessels. Proceedings of the National Academy of Sciences of the United States of America 89, 9504-9508 (1992).
7. Perez-Pomares, J. M. et al. Origin of coronary endothelial cells from epicardial mesothelium in avian embryos. The International journal of developmental biology 46, 1005-1013 (2002).
8. Cai, C. L. et al. A myocardial lineage derives from Tbx18 epicardial cells. Nature 454, 104-108, doi: 10.1038/nature06969 (2008).
9. Smart, N. et al. Thymosin beta4 induces adult epicardial progenitor mobilization and neovascularization. Nature 445, 177-182, doi: 10.1038/nature05383 (2007).
10. Zhou, B. et al. Epicardial progenitors contribute to the cardiomyocyte lineage in the developing heart. Nature 454, 109-113, doi: 10.1038/nature07060 (2008).
11. Christoffels, V. M. et al. Tbx18 and the fate of epicardial progenitors. Nature 458, E8-9; discussion E9-10, doi: 10.1038/nature07916 (2009).
12. Rudat, C. & Kispert, A. Wt1 and epicardial fate mapping. Circ Res 111, 165-169, doi: 10.1161/CIRCRESAHA.112.273946 (2012).
13. Wilm, T. P. & Solnica-Krezel, L. Essential roles of a zebrafish prdm1/blimp1 homolog in embryo patterning and organogenesis. Development (Cambridge, England) 132, 393-404 (2005).
14. Que, J. et al. Mesothelium contributes to vascular smooth muscle and mesenchyme during lung development. Proceedings of the National Academy of Sciences of the United States of America 105, 16626-16630, doi: 10.1073/pnas.0808649105 (2008).
15. Zhou, B. & Pu, W. T. Genetic Cre-loxP assessment of epicardial cell fate using Wt1-driven Cre alleles. Circ Res 111, e276-e280, doi: 10.1161/CIRCRESAHA.112.275784 (2012).
16. von Gise, A. et al. WT1 regulates epicardial epithelial to mesenchymal transition through beta-catenin and retinoic acid signaling pathways. Developmental biology 356, 421-431, doi: 10.1016/j.ydbio.2011.05.668 (2011).
17. Cano, E., Carmona, R. & Munoz-Chapuli, R. Wt1-expressing progenitors contribute to multiple tissues in the developing lung. American journal of physiology. Lung cellular and molecular physiology 305, L322-L332, doi: 10.1152/ajplung.00424.2012 (2013).
18. Carmona, R., Cano, E., Mattiotti, A., Gaztambide, J. & Munoz-Chapuli, R. Cells derived from the coelomic epithelium contribute to multiple gastrointestinal tissues in mouse embryos. PLoS One 8, e55890, doi: 10.1371/journal.pone.0055890 (2013).
19. Wagner, K. D. et al. The Wilms tumor suppressor Wt1 is expressed in the coronary vasculature after myocardial infarction. FASEB J 16, 1117-1119, doi: 10.1096/fj.01-0986fje (2002).
20. Duim, S. N., Kurakula, K., Goumans, M. J. & Kruithof, B. P. Cardiac endothelial cells express Wilms tumor-1: Wt1 expression in the developing, adult and infarcted heart. J Mol Cell Cardiol 81, 127-135, doi: 10.1016/j.yjmcc.2015.02.007 (2015).
21. Haber, D. A., Englert, C. & Maheswaran, S. Functional properties of WT1. Medical and pediatric oncology 27, 453-455, doi: 10.1002/ (SICI)1096-911X(199611)27:5 3.0.CO;2-B (1996).
22. Miyagawa, K. et al. Loss of WT1 function leads to ectopic myogenesis in Wilms tumour. Nature genetics 18, 15-17, doi: 10.1038/ ng0198-15 (1998).
23. Smart, N. et al. De novo cardiomyocytes from within the activated adult heart after injury. Nature 474, 640-644, doi: 10.1038/ nature10188 (2011).
24. Winter, E. M. et al. Preservation of left ventricular function and attenuation of remodeling after transplantation of human epicardium-derived cells into the infarcted mouse heart. Circulation 116, 917-927, doi: 10.1161/CIRCULATIONAHA.106.668178 (2007).
25. Zhou, B. et al. Adult mouse epicardium modulates myocardial injury by secreting paracrine factors. The Journal of clinical investigation 121, 1894-1904, doi: 10.1172/JCI45529 (2011).
26. Morata, G. & Ripoll, P. Minutes: mutants of drosophila autonomously affecting cell division rate. Developmental biology 42, 211-221 (1975).
27. Moreno, E. & Basler, K. dMyc transforms cells into super-competitors. Cell 117, 117-129 (2004).
28. Claveria, C., Giovinazzo, G., Sierra, R. & Torres, M. Myc-driven endogenous cell competition in the early mammalian embryo. Nature 500, 39-44, doi: 10.1038/nature12389 (2013).
29. Villa del Campo, C., Claveria, C., Sierra, R. & Torres, M. Cell competition promotes phenotypically silent cardiomyocyte replacement in the mammalian heart. Cell reports 8, 1741-1751, doi: 10.1016/j.celrep.2014.08.005 (2014).
30. Wessels, A. et al. Epicardially derived fibroblasts preferentially contribute to the parietal leaflets of the atrioventricular valves in the murine heart. Developmental biology 366, 111-124, doi: 10.1016/j.ydbio.2012.04.020 (2012).
31. Arima, Y. et al. Preotic neural crest cells contribute to coronary artery smooth muscle involving endothelin signalling. Nature communications 3, 1267, doi: 10.1038/ncomms2258 (2012).
32. Wu, B. et al. Endocardial cells form the coronary arteries by angiogenesis through myocardial-endocardial VEGF signaling. Cell 151, 1083-1096, doi: 10.1016/j.cell.2012.10.023 (2012).
33. Kikuchi, K. et al. tcf21+ epicardial cells adopt non-myocardial fates during zebrafish heart development and regeneration. Development (Cambridge, England) 138, 2895-2902, doi: 10.1242/dev.067041 (2011).
34. Poelmann, R. E. et al. Evolution and development of ventricular septation in the amniote heart. PLoS One 9, e106569, doi: 10.1371/ journal.pone.0106569 (2014).
35. Verzi, M. P., McCulley, D. J., De Val, S., Dodou, E. & Black, B. L. The right ventricle, outflow tract, and ventricular septum comprise a restricted expression domain within the secondary/anterior heart field. Developmental biology 287, 134-145, doi: 10.1016/j. ydbio.2005.08.041 (2005).
36. Kisanuki, Y. Y. et al. Tie2-Cre transgenic mice: a new model for endothelial cell-lineage analysis in vivo. Developmental biology 230, 230-242, doi: 10.1006/dbio.2000.0106 (2001).
37. Hosen, N. et al. The Wilms tumor gene WT1-GFP knock-in mouse reveals the dynamic regulation of WT1 expression in normal and leukemic hematopoiesis. Leukemia 21, 1783-1791, doi: 10.1038/sj.leu.2404752 (2007).
38. Chen, T. H. et al. Epicardial induction of fetal cardiomyocyte proliferation via a retinoic acid-inducible trophic factor. Developmental biology 250, 198-207 (2002).
39. Garriock, R. J., Mikawa, T. & Yamaguchi, T. P. Isolation and culture of mouse proepicardium using serum-free conditions. Methods 66, 365-369, doi: 10.1016/j.ymeth.2013.06.030 (2014).