Amongst animal species, there is enormous variation in the size and complexity of the heart, ranging from the simple one-chambered heart of Ciona intestinalis to the complex four-chambered heart of lunged animals. To address possible mechanisms for the evolutionary adaptation of heart size, we studied how growth of the simple two-chambered heart in zebrafish is regulated. Our data show that the embryonic zebrafish heart tube grows by a substantial increase in cardiomyocyte number. Augmented cardiomyocyte differentiation, as opposed to proliferation, is responsible for the observed growth. By using transgenic assays to monitor developmental timing, we visualized for the first time the dynamics of cardiomyocyte differentiation in a vertebrate embryo. Our data identify two previously unrecognized phases of cardiomyocyte differentiation separated in time, space and regulation. During the initial phase, a continuous wave of cardiomyocyte differentiation begins in the ventricle, ends in the atrium, and requires Islet1 for its completion. In the later phase, new cardiomyocytes are added to the arterial pole, and this process requires Fgf signaling. Thus, two separate processes of cardiomyocyte differentiation independently regulate growth of the zebrafish heart. Together, our data support a model in which modified regulation of these distinct phases of cardiomyocyte differentiation has been responsible for the changes in heart size and morphology among vertebrate species.
Supplementary material
We thank Dr Cuppen (Hubrecht Laboratory) and Dr Stemple (Welcome Trust Sanger Institute) for providing the isl1k88x zebrafish mutant, which was generated as part of the ZF-MODELS Integrated Project in the 6th Framework Programme (Contract No. LSHG-CT-2003-503496) funded by the European Commission. We also thank R. Kelly for discussions and suggestions when this work was in progress, K. Poss for providing the Tg(cmlc2:dsred2-nuc) fish, A. Moorman and K. Smith for critical reading of the manuscript and members of the Bakkers laboratory for stimulating discussions. Work in J.B.'s laboratory was supported by the Royal Dutch Academy of Arts and Sciences. Work in D.Y.'s laboratory was supported by the National Institutes of Health. E.d.P. was supported by EU FP6 grant LSHM-CT-2005-018833, EUGeneHeart. S.M. was supported by the GABBA program and the Portuguese Foundation for Science and Technology (POCI 2010-FSE). Deposited in PMC for release after 12 months.