- Open Access
Outflow tract septation and the aortic arch system in reptiles: lessons for understanding the mammalian heart
- Robert E. Poelmann1, 2Email author,
- Adriana C. Gittenberger-de Groot1,
- Marcel W. M. Biermans2,
- Anne I. Dolfing2,
- Armand Jagessar2,
- Sam van Hattum2,
- Amanda Hoogenboom2,
- Lambertus J. Wisse3,
- Rebecca Vicente-Steijn1, 3,
- Merijn A. G. de Bakker2,
- Freek J. Vonk2, 4,
- Tatsuya Hirasawa5,
- Shigeru Kuratani5 and
- Michael K. Richardson2
© The Author(s) 2017
Received: 21 February 2017
Accepted: 3 May 2017
Published: 10 May 2017
Cardiac outflow tract patterning and cell contribution are studied using an evo-devo approach to reveal insight into the development of aorto-pulmonary septation.
We studied embryonic stages of reptile hearts (lizard, turtle and crocodile) and compared these to avian and mammalian development. Immunohistochemistry allowed us to indicate where the essential cell components in the outflow tract and aortic sac were deployed, more specifically endocardial, neural crest and second heart field cells. The neural crest-derived aorto-pulmonary septum separates the pulmonary trunk from both aortae in reptiles, presenting with a left visceral and a right systemic aorta arising from the unseptated ventricle. Second heart field-derived cells function as flow dividers between both aortae and between the two pulmonary arteries. In birds, the left visceral aorta disappears early in development, while the right systemic aorta persists. This leads to a fusion of the aorto-pulmonary septum and the aortic flow divider (second heart field population) forming an avian aorto-pulmonary septal complex. In mammals, there is also a second heart field-derived aortic flow divider, albeit at a more distal site, while the aorto-pulmonary septum separates the aortic trunk from the pulmonary trunk. As in birds there is fusion with second heart field-derived cells albeit from the pulmonary flow divider as the right 6th pharyngeal arch artery disappears, resulting in a mammalian aorto-pulmonary septal complex. In crocodiles, birds and mammals, the main septal and parietal endocardial cushions receive neural crest cells that are functional in fusion and myocardialization of the outflow tract septum. Longer-lasting septation in crocodiles demonstrates a heterochrony in development. In other reptiles with no indication of incursion of neural crest cells, there is either no myocardialized outflow tract septum (lizard) or it is vestigial (turtle). Crocodiles are unique in bearing a central shunt, the foramen of Panizza, between the roots of both aortae. Finally, the soft-shell turtle investigated here exhibits a spongy histology of the developing carotid arteries supposedly related to regulation of blood flow during pharyngeal excretion in this species.
This is the first time that is shown that an interplay of second heart field-derived flow dividers with a neural crest-derived cell population is a variable but common, denominator across all species studied for vascular patterning and outflow tract septation. The observed differences in normal development of reptiles may have impact on the understanding of development of human congenital outflow tract malformations.
In mammals, the normal formation of the aorto-pulmonary septal complex has been analysed mostly in the setting of the description of mutant mice or manipulated avian embryos, resulting in outflow tract malformations including malalignment of the outflow tract (OFT) septum, asymmetric arterial development (Tetralogy of Fallot), transposed great arteries (TGA) and absent separation of the great arteries, resulting in a persistent truncus arteriosus (common arterial trunk) [1–3]. It is evident that remodelling of the myocardial OFT at the junction with the vascular aortic sac is complex and employs different cell populations (myocardium, endocardial cushions, neural crest and mesenchymal second heart field) to various degrees [4–6]. Here, we concentrate mostly on three levels of the developing heart, the proximal outflow tract (also called the conus arteriosus), the distal outflow tract (truncus arteriosus) and the pharyngeal arch arteries emerging from the aortic sac. The remodelling of the branchial or pharyngeal arch system is one of the hallmarks of amniote development. The pharyngeal arches encompass key structures including neuronal, supportive, muscular and vascular elements together making up parts of the face, neck and upper thoracic region . The pharyngeal arch arteries (PAAs) in reptiles and birds (sauropsids) and in mammals develop in a craniocaudal sequence as shunts between the aortic sac and the paired dorsal aortae. The mode of PAA remodelling is essential for understanding OFT separation connecting the aortic sac to the non-septated ventricular (most reptiles) or biventricular heart (crocodiles, mammals and birds). The latter results invariably in one single pulmonary trunk, dividing into a right and left pulmonary artery (PAA6), connected to the right ventricle, or the right-sided cavum pulmonale of the common ventricle. In the species studied, this is combined with two aortae (left and right PAA4) in the lizard, turtle, crocodile and early embryonic bird. The left visceral aorta arises from the cavum venosum of the common ventricle, whereas the right systemic aorta emerges from either the left ventricle, or the cavum venosum receiving blood from the cavum arteriosum. In birds, the left PAA4 disappears early in development leaving a right PAA4 which forms a right-sided aortic arch in the mature animal. In crocodiles, the right PAA4 arises from the left ventricle; this becomes the systemic aorta, supplying, for example, the cranial and brachial regions and the body wall with oxygen-rich blood. However, the left PAA4, supplying the viscera, arises from the right ventricle together with the pulmonary trunk. Therefore, the left PAA4 has also been called the visceral aorta . In mammals, the aortic trunk arises from the left ventricle and the left PAA4 will form the left-sided aortic arch, while the right PAA4 forms the basis of the right subclavian artery.
Remodelling of the OFT and the aortic sac with the emerging PAAs requires the involvement of several cell populations. First of all, extracardiac cells from the postotic rhombencephalic neural crest contribute to this area [9, 10]. Furthermore, at this level the vessels are embedded in the second heart field [11–13], which is part of the splanchnic mesoderm, encompassing also the coelomic lining of the pericardial cavity that gives origin to the arterial epicardial cells [14, 15]. The synchronized development of these cell populations results in the formation of OFT myocardium and endocardial cushions, in conjunction with the aorto-pulmonary septum [4–6] and the wall of the arterial trunks [2, 10, 16–18] in a narrow time window.
Ventricular septation is a complex process, involving not only the myocardial wall but also the overlying epicardium. Recently, we distinguished the ventral part of the interventricular septum as the folding septum . As it is located adjacent to the outflow tract, the relation with the proximal conal endocardial cushions, more specifically the septal cushion, is of interest. Not only does the separation at intracardiac and arterial level show variations, but the remodelling in the distal segments of the PAAs is also variable between species. In all taxa investigated, the connection of PAA3 with the paired dorsal aortae (carotid ducts) disappears. In reptiles including birds, the left and right PAA6 (ductus arteriosus), connecting to the dorsal aortae, persist until hatching. In many reptiles, they persist even after hatching as in Sphenodon, Testudines, several species of lizards and snakes, and maybe even in some crocodiles; for detailed comparative descriptions, see [20–23]. In mammals, the right PAA6 disappears early in development, while the left PAA6 persists until birth as the ductus arteriosus of Botalli [24, 25]. Although complete anatomical septation at the level of the left and right ventricle takes place in crocodiles, both anatomical and functional separation of pulmonary and systemic blood flows remain incomplete, as a central shunt between the roots of both aortas provides a direct communication between left and right ventricular outflows. The development of this foramen of Panizza (as first described by Bartolomeo Panizza in 1833, see Ref. ) adds to the complexity of the crocodilian circulation.
This complex diversification resulting from the evolutionary remodelling of a symmetric ancestral PAA system including the (septating) heart has been used to provide characteristics in phylogeny reconstruction [7, 20, 23, 26, 27]. The position of the Testudines, for example, has been contentious, because embryological, morphological and molecular data can yield conflicting phylogenies. Thus, it has been variously suggested that turtles are a basal reptilian clade , a sister group to lepidosaurs  or sister group to the archosaurs (together forming the Archelosauria) [30–34].
Basic to the circulatory system is the beating heart providing the propelling force for the arterial blood flow, and the resulting haemodynamic forces are in themselves an important modifier of development [35–38], allowing shear stress responsive genes such as endothelin1, KLF2 and NOS3 to enter the stage . Modulation of these and other genes in mouse models often results in cardiovascular malformations.
The aim of this study is to examine, in a comparative evolutionary developmental biology context: (1) the respective roles of various cell populations (second heart field, endocardial and neural crest cells) in the morphogenesis of both the interaortic flow divider and the aorto-pulmonary septum between the aortic and the pulmonary trunks so as to produce three arterial trunks from the aortic sac: the left (visceral) and right (systemic) aorta as well as the pulmonary trunk; (2) the cellular mechanisms underlying the septation of the intracardiac outflow tract in reptiles, which is minimal in lizards and turtles and becomes myocardialized in crocodiles and birds.
We use an integrative ‘evo-devo’ approach encompassing comparative morphology, developmental biology and protein expression patterns in embryonic cell populations. Specifically, we apply (immuno-)histochemistry to serially sectioned embryos and implement Amira-based 3-D reconstructions to reveal the spatiotemporal remodelling of the outflow tract and PAAs. We have applied this approach by sampling the following taxa: agamid lizards (bearded dragon, Pogona vitticeps), Testudines (the soft-shell turtle Pelodiscus sinensis), crocodiles (Nile crocodile, Crocodylus niloticus), and birds (chicken, Gallus gallus). We analyse our findings also in the context of what is described in the literature about the corresponding processes in mammals. In mammals [2, 18] and birds [9, 10, 12], the dual contribution of both second heart field and neural crest to the aortic root and the aorto-pulmonary septal complex has been described. We will demonstrate that in birds the position of the aortic flow divider and in mammals the pulmonary flow divider are essential for understanding the formation of the aorto-pulmonary septal complex.
Materials and methods
Pelodiscus sinensis eggs were purchased from a Japanese local farm and incubated at 30 °C, and the embryos were fixed at different developmental stages at the Evolutionary Morphology Laboratory, RIKEN (Kobe, Japan). The crocodile embryos were obtained from La Ferme aux Crocodiles (Pierrelatte, France). Bearded dragons were obtained through local breeders, and specific pathogen-free chicken eggs from a commercial source.
Comparison of the stages of the various species studied
We used the stages provided by Sanger et al.  (Anolis comparable to Pogona), Tokita and Kuratani  (Pelodiscus) and Ferguson  (Alligator for Crocodylus). Our experience reveals this to be practical for use in comparing cardiovascular development between reptiles, notwithstanding differences in developmental stages between species due to heterochrony in several organ systems , which becomes particularly evident after approximately HH stage 32.
Fixation and histology
Embryos were fixed for 24–48 h in buffered 4% paraformaldehyde at 4 °C. They were stored in methanol 100% at −20 °C until further use. Chicken embryos were stored in 70% ethanol at 4 °C. Subsequently, the embryos were transferred to 100% ethanol and embedded in paraffin with Histo-Clear II (National Diagnostics, Atlanta, Georgia, USA) as the intermediate reagent. Thoracic blocks of tissue, containing the heart and pharyngeal arch arteries, were serially sectioned (5 µm) and mounted on objective slides allowing for five different sequential stainings of sister sections. As a standard, one set of sister sections was stained with hematoxylin–eosin. In addition, selected specimen were stained using the Movat or Sirius red procedure to demonstrate components such as elastin, collagen, glycosaminoglycans (GAGs) and (smooth) muscle (immunohistochemistry was also used as described below).
Paraffin sections were histologically stained according to slightly modified procedures as described in Bancroft and Gamble (6th ed. 2008). This holds for the haematoxylin–eosin staining, the Russell modification of the Movat Pentachrome staining and the Sirius Red staining.
We chose to use immunohistochemical staining protocols as these can be applied to the fixed and variously stored material of the species under study. Adjacent sister sets of sections were stained with a selection of antibodies for MLC2a (myosin light chain for myocardium) or CTNI (cardiac troponin I for myocardium); homeobox protein NKX2–5 (myocardial cells and SHF cardiac precursors), HNK1 for early migrating neural crest cells, the transcription factor TFAP2α (activator of protein, for migrating neural crest cells) , Isl1 for second heart field cells, WT1 (Wilms tumour-like 1 for embryonic mesothelium (epicardium, pericardium) including associated mesenchymal cells [47, 48].
Paraffin sections for immune incubations were dewaxed in Histo-Clear, rehydrated via a decreasing percentage of ethanol and microwaved for 12 min in 0.01 M citric buffer pH 6.0 for antigen retrieval. Endogenous peroxidase was inhibited using 0.3% H2O2 in phosphate-buffered saline (PBS) for 20 min and the sections rinsed in PBS.
For staining sections, the first antibodies were diluted in BSA/PBS and incubated overnight at room temperature (Isl1, 1/100;CTNI, 1/800; NKX2–5 1/2000; TFAP2α 1/500; WT1 1/3000; MLC2a 1/6000; HNK1, 1/10). The WT1 staining was performed on freshly sectioned material. The antibodies were raised in rabbit, except for NKX2.5 (in goat) and Isl1 and HNK1 (in mouse).
The second antibody depended on the species in which the first antibody was obtained, and was applied as follows: Isl1: 60-min horse anti-mouse 1/200 in horse serum; CTNI: 60-min goat anti-rabbit-biotin, 1/200 in goat serum; NKX2.5: 60-min horse anti-goat-biotin 1/66 in horse serum; TFAP2α: 45-min goat anti-rabbit biotin 1/200 in goat serum; WT1: 60-min goat anti-rabbit biotin 1/200 in goat serum; MLC2a: 60-min goat anti-rabbit biotin 1/200 in goat serum. HNK1: 120-min rabbit-anti-mouse 1/250 in bovine serum.
The procedures were finalized by ABC reagents (avidin-biotinylated complex) according to manufacturers’ protocol: 45 min. Visualization took place by DAB/H2O2 (10 min) followed by rinsing in demineralized water. Sections were briefly counterstained with haematoxylin, dehydrated and coverslipped with Entellan.
Primary antibodies were obtained from Vector labs (Isl1, second antibodies, ABC reagents), Santa Cruz (CTNI, NKX2–5, WT1), Gene Tex (TFAP2α), and Hybridoma Bank (HNK1).
Images of high quality and resolution were created using the Philips Ultra Fast Scanner 1.6 (Dept. Pathology, Leiden University Medical Centre (LUMC), Leiden). Images were imported into the database Philips Image Management System (IMS), which has the benefits of working digitally and allow to view multiple images simultaneously. The selected material for 3D reconstruction all met the following criteria: clearly visible (immuno)staining, no important structures for heart development missing, and sections were positioned in the correct order to follow-up for Amira. Construction of the 3-D models was done in Amira version 5.3.3 (FEI Visualization Sciences Group, Bordeaux). First, the images were optimized by cropping and enhancing the contrast. Voxel size was determined, and images were loaded into Amira. After that, the various structures were selected and reconstructed three-dimensionally. Segmentation of the structures studied was based on a combination of histology and immune staining patterns. Finally, reconstructions were converted into 3-D pdfs allowing study of the whole reconstruction database or of a subset of elements, as, for instance, only the pharyngeal arch arteries.
Pharyngeal arch arteries 1–6
- Aortic sac:
Common vessel connecting the myocardial OFT to the respective arterial trunks
- Carotid trunk:
Combined stem of the left and right PAA3, joining the right PAA4
- Carotid duct:
(Disappearing) segment of the dorsal aorta between PAA3 and PAA4
- Aortic trunk:
Combined stem of the left and right PAA4
- Pulmonary trunk:
Combined stem of the left and right PAA6, emerging from the right ventricle or cavum pulmonale
- Systemic aorta (sAo):
Right-sided PAA4, emerging from the left ventricle or the cavum venosum-cavum arteriosum combination
- Visceral aorta (vAo):
Left-sided PAA4, emerging from the right ventricle or cavum venosum; this artery disappears early in birds
- Ductus arteriosus:
PAA6 connecting the pulmonary trunk to the respective dorsal aortae, the right-sided PAA6 disappears early in mammals.
Notes on the OFT cushions
Summary of principal differences
Short left visceral aorta
Short right systemic aorta
Long aortic trunk, bifurcating
Unseptated outflow tract
Completely septated ventricles
Parietal OFT cushion in conus
SHF in PAA4 and PAA6 flow divider
AP septal complex
NCC in muscular AP septum
NCC (TFAP2α) in PAA3
Foramen of Panizza (FOP)
Chicken (G. gallus)
In later stages (HH22 and onwards), the number of TFAP2α staining cells (NCC) in the mesenchyme of the pharyngeal arches diminishes dramatically, due to downregulation in the differentiating NCC, as specific cells in the neural tube remain positive, proving that the staining protocols are adequate. Therefore, in the chicken we used alternative markers to distinguish NCC from second heart field-derived cells. To that aim the second heart field ‘marker’ ISL1 was used, leaving NCC negative (Fig. 1b, c). Similarly, WT1 marking the coelomic epithelial lining and its mesenchymal cells allows visualization of non-NCC in the arterial pole (Fig. 1d–f).
The carotid trunk (the common left and right PAA3) together with the right PAA4, but excluding the disappearing left PAA4, shares a common stem (aortic trunk) upon leaving the heart, and this aortic trunk is parallel to the pulmonary trunk (Fig. 2f). The separated left and right PAA6 are asymmetrically located where they leave the heart. In particular, the right PAA6 changes position to dorsal and right. It is important to stress that both PAA6 persist until hatching, whereas in mammals only the left PAA6 persists until birth.
In HH31–33, the aorto-pulmonary septum still carries apoptotic cells between the left and right ventricular OFTs. OFT septation is now completed. Thick semilunar valve leaflets are present. The pulmonary and aortic trunks are separated, and mesenchymal WT1-positive cells are still present between the aortic and pulmonary arteries (Fig. 3g, h). A coronary artery ostium is present in the aortic root at the sinus of Valsalva (not shown). Remodelling of the PAAs is complete.
Bearded dragon (P. vitticeps)
Development of the OFT and PAAs in the bearded dragon shows a number of differences from that described above for the chicken. Most obvious are the absence of a cardiac interventricular septum, and the persistence of both the left visceral and right systemic aorta in addition to the pulmonary trunk (for a summary of the major features, see Table 2).
In HH26, three arterial stems emerge from the aortic sac; these are the pulmonary, the aortic and the carotid trunks. Shortly after leaving the aortic sac, these trunks divide symmetrically into their arteries comprising PAA 6, 4 and 3, respectively. They terminate in the left and right dorsal aortae.
In the next stage (HH28), both septal and parietal cushions, connected to each other by a thickened cellularized endocardium, are present in the proximal OFT. Distally, four cushions are present, although not exactly at the same level. The septal cushion contains an inconspicuous whorl-like core, considerably less massive than the condensed mesenchyme seen in a comparable stage and location in the chicken. Neural crest participation in this whorl could not be found by TFAP2α staining. Where the myocardial sleeve meets the arterial walls, the septal cushion fuses asymmetrically with the broadened parietal cushion, separating the pulmonary and aortic channels (Fig. 4c). Slightly more distally the septal cushion again fuses asymmetrically, this time with a part of the lateral aortic intercalated cushion, dividing the left visceral and right systemic aorta.
In the distal outflow tract of HH29.5, the large septal cushion (Fig. 4d) contains an indistinct body of condensed mesenchyme, which shows a few apoptotic cells (Fig. 4e); these are less abundant than in the same location in the chicken heart. The septal cushion has fused in two places: first with the parietal (Fig. 4d) and next with the aortic intercalated cushion (Fig. 4f). The pulmonary intercalated cushion is not involved in OFT separation. Distal to the myocardium the pulmonary trunk shifts to a more dorsal position and splits into both PAA6 of which the right one reaches a more cranial axial level. In the oldest stages studied (HH34, 36), the condensed mesenchyme in the fused cushions remains as indistinct as in the earlier stages.
Chinese soft-shell turtle (P. sinensis)
At HH27, the proximal OFT contains only a septal cushion and not a parietal one, although the subendocardium is cellularized. In the distal OFT, four cushions are present. Many cells in the tunica media of the carotid trunk including the branches of the left and right PAA3 stain heavily for TFAP2α (Fig. 5c), indicating the presence of NCC. The other PAAs do not present with positive cells. Likewise, the AP septum between pulmonary and aortic trunks is negative for TFAP2a, possibly downregulated in the NCC. A 3D reconstruction demonstrates the location of the condensed mesenchyme of the AP septum (green in Fig. 5d, e).
Although the septal cushion remains negative for TFAP2α (Fig. 6c), it shows condensed mesenchyme indicative of the presence of NCC probably differentiating into cartilage . More downstream the pulmonary trunk divides into both PAA6 (Fig. 6f), while the left visceral aorta does not branch at all. The right systemic aorta gives off the carotid trunk, which is still positive for TFAP2α (Fig. 6g) and rich in extracellular matrix glycosaminoglycans giving it a spongy appearance (Fig. 6h). Both carotids branch into the left and right subclavian arteries (not shown) as is the case in all reptilian embryos of comparable developmental stage investigated here. Additionally, another turtle of which the cardiac development has been described by our group  was re-investigated for the embryonic architecture of the carotid artery. In Emys orbicularis, the carotid artery lacks the spongy appearance (Fig. 6i).
Crocodile (C. niloticus)
In HH18, the OFT cardiac jelly is sparsely cellularized; a septal and a less distinct parietal cushion is already present.
The pulmonary trunk is embraced by a ventral and by a dorsal myocardial protrusion into the fused septal/parietal cushion that flanks the continuation of the folding septum (Fig. 8d, e). The two inward protrusions of myocardium almost meet in the centre, but are separated by condensed mesenchyme, presumably NCC-derived (compare Fig. 8d, e, *). The aortic flow divider also extends from the septal cushion but in this case towards the right intercalated cushion (as in Pogona and Pelodiscus), thereby separating the two aortae (#). Coronary ostia above the septal and intercalated cushion of the right systemic aorta are evident from this stage onwards. The total number of ostia observed in a specimen is 4–5.
Formation of the semilunar valves
The three separated arterial trunks show a different arrangement of endocardial cushions (Fig. 8g). The large septal cushion delivers valve elements to each of the three arterial trunks, similar to what was observed in Pelodiscus. In summary, the right systemic aorta contains two large cushions, whereas the left visceral aorta and the pulmonary trunk each contain two large cushions and a small one. Note that for easy understanding relevant 3D levels are combined in one 2D cartoon in Fig. 8g.
Septation of the aortae and the pulmonary channels is by involvement of NCC-derived condensed mesenchyme connecting the ventral with the dorsal myocardium (Fig. 9f, g). Condensed mesenchyme is present near the distal tip of the cartilage in the septal cushion bordering the lumen of the foramen of Panizza, flanking the folding septum (Fig. 9c–e). Slightly further downstream the vessel walls are completely separated (Fig. 9g, h) harbouring the valve leaflets. Essentially, the systemic aortic valve is bicuspid (Fig. 9e, g) as is the case with the pulmonary valve (Fig. 9g, h, see also Fig. 8g).
One important consideration in our study is the assumption that our cross-species comparisons are based on comparable stages. It is always difficult to compare stages in different taxa because of confounding factors such as heterochrony . Nonetheless, we can at least use homologous characters such as staining profiles, tissue architecture, endocardial cushion formation and fusion, mesenchymal condensation and cartilage formation  to compare developmental sequences in the different species studied. And to assist this task, we used chicken stages as a reference.
Comparative cardiac septation in reptilian evolution
Cardiac septation within the reptilians and birds (sauropsids) differs significantly among taxa. Lizards and snakes (squamates) and turtles (Testudines) show no ventricular and OFT septation , whereas crocodiles and birds (archosaurs) have a biventricular heart with concomitant myocardial OFT separation. We will argue that the squamate heart shows the primitive condition for extant sauropsids, while the archosaur heart is highly derived. The turtle heart more closely resembles the squamate heart . This is perhaps surprising in view of the hypothesis that turtles are a sister group to the archosaurs, the two together constituting the Archelosauria . However, it is possible that the turtles retain the primitive condition because they are, like the squamates, exothermic, and have therefore never evolved the specializations of the heart (including complete ventricular septation) seen in the endothermic mammals and birds, and in the ectothermic crocodilians where the fully septated ventricle may reflect an ancestral endothermic condition for the archosaurs .
The birds are unique among the reptiles, and even the amniotes, because the left PAA4 disappears between HH28 and 32, accompanied by apoptosis. The right PAA4 supplies the entire systemic circulation. Even crocodiles, the closest living relatives of birds retain the left PAA4 as a visceral aorta that mostly serves the digestive system. In all species studied here, the right PAA4 is a branch of the systemic aortic trunk from which the carotid trunk branching in the left and right PAA3 and subsequently the subclavian arteries arise. In mammals, the subclavian arteries are branches of the PAA4.
Endocardial cushions and septation
In this study, the outflow tract is considered to be the myocardial tube with its enclosed endocardial cushions, while the mesenchymal aortic sac is considered to give rise to the arterial trunks. Septation encompasses both the OFT and the aortic sac. Septation in archosaurs involves the formation of a multicomponent complex; homologs of the constitutive elements of this complex can be found, unfused, in turtles and in squamates. Proximally, in early stages of development in Pogona, Pelodiscus and Crocodylus there is a septal cushion and in addition a layer of cellularized endocardium instead of a parietal cushion. The absence of a parietal cushion in Pogona and its relatively late appearance in Pelodiscus may be related to the absence of ventricular septation in these species. In later stages (Pelodiscus, Crocodylus), both a septal and parietal cushion are present.
Distally, the OFT of all species contains four intramyocardial endocardial cushions of which the dorsally located septal cushion is the largest. The septal cushion continues through the length of the OFT in all species, providing a hemodynamic separation for the pulmonary and aortic channels. The proximo-distal continuation of the other cushions is variable as there are maximal 2 proximal cushions but 4 distal cushions (see Ref.  for divergent descriptions). The proximal part of the septal cushion contains the neural crest-derived condensed mesenchyme in chicken. The typical whorl configuration is least evident in Pogona, the species that lacks the continuous parietal cushion, and shows no OFT myocardialization at all. Arterial separation remains mesenchymal in Pogona. Distal cardiac outflow tract septation shows some myocardialization in Pelodiscus, but is only fully myocardialized in Crocodylus and Gallus. Completion of interventricular septation shows heterochrony when the chicken and crocodile are compared. The oldest crocodile embryo studied (comparable to chicken HH40) still exhibits an interventricular communication that in chicken is closed much earlier, between HH32 and 35.
Endocardial cushions and semilunar valve formation
The four distal endocardial cushions participate unequally in the formation of the ‘semilunar’ valve leaflets. The large dorsally located septal cushion separates in three parts, one for each arterial trunk. Because of the asymmetric fusion of the septal with the aortic intercalated cushion, the major segment of the latter becomes attributed to the right systemic aorta, whereas a smaller segment is allotted to the left visceral aorta. Again, because of a second asymmetric fusion with the parietal cushion, the major segment of the parietal cushion can be found in the lumen of the visceral aorta, with a smaller segment allotted to the pulmonary trunk, where also the pulmonary intercalated cushion can be found. It is evident that a bicuspid valve is the outcome in all three arterial trunks. The smaller cushion segments probably do not participate in leaflet formation.
In birds and mammals, no asymmetric cushion fusion is observed, and both the dorsal and parietal cushion deliver comparable amounts of cushion tissue to aortic and pulmonary trunks, and together with the intercalated cushion tissue, form arterial valves with three leaflets. In humans, a bicuspid aortic valve is the most common congenital cardiac malformation. The mechanism is poorly understood, but the end result is usually described as an abnormal fusion of cushions/leaflets  but may also result from absence of one of the participating endocardial cushions.
Neural crest, second heart field and septation
It is fortunate that NCC and SHF derivatives could be traced in most reptile species immunohistochemically, at least in early stages, using a combination of TFAP2α for NCC , and Isl1  and WT1 staining  for the non-NCC. Non-NCC relevant for this area is the SHF cells [2, 6]. We use WT1 as marker for a subpopulation of the splanchnic mesoderm that forms such tissues as the mesothelial lining of the body wall , which in turn gives rise to the epicardium and pericardium. The arterial epicardium [14, 15, 57] covers the arterial roots as described here. Whether the WT1 positive mesenchyme in the arterial pole derives from the epicardial epithelium or vice versa is uncertain as WT1 is able to activate both epithelium–mesenchyme transition and mesenchyme–epithelium transition . In organogenesis of the metanephric mesenchyme , WT1 regulates gene networks involving Wnt/beta catenin, hedgehog, LRP2, retinoic acid, FGF8/10 and BMP4 signalling, among others. Several of these genes are expressed in the pharyngeal mesoderm, making WT1 a useful marker for SHF cells at the arterial pole.
Chicken and quail-chicken chimeras [6, 10, 16, 58, 59] have provided solid evidence of the NCC and SHF distribution, while genetic markers provided similar evidence in mice [2, 4, 5, 18]. However, in older stages of development the distinction between cell populations is lost, probably due to downregulation of gene expression.
Separation of the two aortic channels is similar in all reptile species investigated here. The involvement of the arterial wall (SHF in the proximal vessel wall and NCC more distally according to chicken and mouse data) is evident in Pogona, Pelodiscus and Crocodylus. In the crocodile, the intracardiac aorto-pulmonary level is most complex, as it includes the foramen of Panizza, abutted by cartilage , channelling through the aortic half of the distal septal cushion and joining the lumina of the visceral and the systemic aorta, but not the pulmonary trunk. Either the NCC or the growing myocardial barrier here is probably preventing the foramen of Panizza from developing in the pulmonary third of the distal septal cushion. The facing semilunar valve leaflets of both aortae covering the outlets of the foramen may serve secondarily as a valve flap, stopping interaortic flow during systole both to prevent high pulmonary pressure and to facilitate a shunting flow during diving in adults . It is reported that in adult crocodiles only the medial leaflet of the right aortic valve covers the foramen during systole, strengthening the idea that blood flow to the brains is favoured even under prolonged diving conditions .
In Gallus, the situation is different as between HH28 and 32 the left visceral aorta disappears accompanied by apoptosis (see further relevance below), thereby escaping from the septation complex. The consequence is a merging of the interaortic SHF elements (PAA4 flow divider) with the aorto-pulmonary NCC elements (aorto-pulmonary septum) into the definitive aorto-pulmonary septal complex, containing both cell derivatives [10, 59, 62]. It is attractive to search for homologies with mammalian development. We have to realize that in mammals both PAA4 persist, the left one turning into the aortic arch, and the right one that will be incorporated into the right subclavian artery. Mouse OFT development shows that here the subdivision in a right and left PAA4 occurs more downstream than in the reptiles including birds. However, in mammals the interpulmonary flow divider between left and right PAA6 is adjacent to the aorto-pulmonary separation  together constructing the aorto-pulmonary septal complex. Aorto-pulmonary separation in mammals and reptiles occurs similarly at the myocardial–arterial junction, but the right PAA6 disappears in mammals. As a consequence, in mammals the aorto-pulmonary septal complex contains both NCC- and SHF-derived elements related to PAA6 [18, 62], whereas in birds the aorto-pulmonary septal complex contains NCC and SHF elements related to PAA4. In the other reptiles, the left aorta is caught between the aortic flow divider and the aorto-pulmonary septum keeping the constituent cell populations mostly separated. Abnormalities in either SHF or NCC may cause a shift in one of the constituents resulting in congenital malformations of the outflow tract and aorto-pulmonary septation [2, 3, 63].
OFT and apoptosis
Apoptosis in the myocardium and in the mesenchymal AP septal complex including NCC [24, 64–69] has been attributed diverse functions. These include shortening of the OFT, ingrowth of the coronary arteries, separation of the pulmonary and aortic channels, remodelling of the pharyngeal arch arteries (left PAA4 in birds, right PAA6 in mammals), activation of growth factors, and myocardialization of the intracardiac OFT. All these phenomena occur in the same time window, at the same location but in different cell populations. Myocardial apoptosis may be instrumental in, e.g. shortening of the OFT  and coronary ingrowth , whereas mesenchymal apoptosis may add to aorto-pulmonary separation and myocardialization of the septum [65, 66] or final migration of NCC .
In a previous study, we showed a high incidence of apoptosis in embryos concomitant with myocardialization and with the unique disappearance of the left PAA4 and right PAA6 . In Pogona lacking both remodelling of the PAA4 and myocardialization, apoptosis was inconspicuous, at a low level in Pelodiscus, but more frequent in Crocodylus and also in mammals, all with persisting PAAs. It is attractive to bestow signalling by apoptotic NCC a major function in myocardialization of the outflow tract [16, 64].
Carotid artery differentiation in Pelodiscus
The carotid trunk and carotid arch arteries (PAA3) in Pelodiscus differ from the other PAAs and arterial trunks with respect to histology. Furthermore, we confirmed the presence of TFAP2α-positive NCC in the cells of the tunica media of the PAA3. In addition, in the crocodile outer cells of the tunica media also expressed TFAP2α, albeit more diffusely. In Pelodiscus histology showed a spongious mesenchyme of the tunica media, containing abundant extracellular matrix glycoproteins which is probably less compressible because of the high water content of this matrix. A short survey of available slides  of the turtle E. orbicularis proved that here this carotid specialization is absent in showing no differences between the various PAA3, 4 or 6. Pelodiscus and other soft-shell turtles dive for prolonged times (for instance during hibernation), using buccopharyngeal respiration. Specifically, the buccopharyngeal membrane contains many highly vascularized villi . Increased pharyngeal movements assist in increased O2/CO2 exchange as well as in urea excretion [71, 72]. These functions probably need some kind of regulation of the blood supply. Functionally, carotid vascular relaxation in these turtles might help to provide the buccopharyngeal area with extra blood, while constriction will turn the haemodynamics to base level. Further studies are needed to examine these issues. The vascular architecture in crocodiles showed no overt differences between PAAs, but crocodiles use the foramen of Panizza as a central shunt between the visceral and systemic aortae, serving another function by providing the brain with additional blood during diving exercise.
Coronary arterial ostium development in Crocodylus
Development of the coronary vascular system depends on many interactions including the sinus venosus-derived endothelium and the epicardium-derived smooth muscle cells [73, 74]. The formation of the stems of the coronary arteries by the ingrowth into the aorta has been described in birds and mammals [75, 76] and is modulated by contact with the aortic endothelium and regulated by differential Tbx1 expression responsible for differences in left/right ingrowth . Usually, in mammals the left and right coronary ostia can be found in the sinus of Valsalva of the left and right leaflet of the aortic semilunar valve, while the aortic intercalated leaflet and the pulmonary trunk are in most cases devoid of a coronary ostium. In reptiles, the coronary arterial circulation differs among taxa . Crocodiles have two aortas, each with bicuspid valve leaflets, and both leaflets of the systemic aorta but not the visceral aorta nor the pulmonary trunk harbour coronary ostia in their sinuses. Future research on such factors as Tbx1 expression patterns in crocodiles could elucidate the mechanisms of coronary ingrowth in a naturally occurring bicuspid aortic valve and shed light on the possible homology of the different endocardial cushions and the leaflets derived from them.
Outflow tract septation in Amniotes requires the coordinated differentiation of myocardium, endocardium, neural crest and second heart field-derived cells. This takes place in conjunction with the upstream septation of the ventricle and the downstream remodelling of the pharyngeal arch arteries. In lizards and turtles, septation of the ventricle is incomplete, while crocodiles, birds and mammals present with a completely septated left and right ventricle. Early embryos of reptiles including birds present a systemic aorta, emerging from the left-sided (part of the) ventricle providing the main parts of the body. Furthermore, they have a pulmonary trunk providing the lungs and a visceral aorta, mainly for the digestive system. Both emerge from the right-sided (part of the) ventricle. In bird embryos, the left-sided visceral aorta disappears later by apoptosis. In mammals, only the systemic aortic and pulmonary trunks emerge from their respective ventricles, but here the right-sided pulmonary 6th pharyngeal arch artery will disappear early in development. The cells contributing to the septation complexes in the reptiles studied consist of the neural crest-derived aorto-pulmonary septum between aortic and pulmonary trunks. In birds, the second heart field-derived aortic flow divider joins the aorto-pulmonary septum (avian aorto-pulmonary septal complex) as the visceral aorta disappears, while in mammals the pulmonary flow divider will merge with the aorto-pulmonary septum (mammalian aorto-pulmonary septal complex) as the right 6th pharyngeal arch artery will disappear.
In crocodiles, the two persisting aortae have a connection, the foramen of Panizza, allowing shunting of blood, while in the lizard and turtle the shunting occurs at the level of the non-septated ventricle. Although turtles, crocodiles and birds are grouped in the recently formed clade of the Archelosauria, cardiac development of the turtle resembles more closely that of the lizard.
REP and ACGdeG devised the concepts and wrote the manuscript; REP and MKR took care of the overview; MWMB, AID, AJ, SvH and AH did the analysis of the embryos; LJW assisted with 3D analysis; LJW and MAGdeB provided the training; RVS provided stained sections; FJV, TH and SK delivered staged embryos. All authors read and approved the final manuscript.
The authors wish to acknowledge Gerda Lamers (IBL), Marlieke Geerts (LUMC) and Saskia Maas (LUMC) for their assistance in histology matters. Dr. Jan Oosting and Brendy van den Akker (department of Pathology, LUMC) supervised the storage of sections in the IMS system. The medical artist Ron Slagter took care of the cartoons.
The authors declare no competing interests.
Funded by Riken to SK.
Under Dutch law, the embryos in the stages used are not considered experimental animals and need therefore no consent from the Animal Experimental Council of the Leiden University and the Leiden University Medical Center.
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- Jain R, Engleka KA, Rentschler SL, Manderfield LJ, Li L, Yuan L, et al. Cardiac neural crest orchestrates remodeling and functional maturation of mouse semilunar valves. J Clin Investig. 2011;121:422–30. doi:10.1172/JCI44244.View ArticlePubMedGoogle Scholar
- Baardman ME, Zwier MV, Wisse LJ, Gittenberger-de Groot AC, Kerstjens-Frederikse WS, Hofstra RM, et al. Common arterial trunk and ventricular non-compaction in Lrp2 knockout mice indicate a crucial role of LRP2 in cardiac development. Dis Models Mech. 2016;9:413–25. doi:10.1242/dmm.022053.View ArticleGoogle Scholar
- Anderson RH, Chaudhry B, Mohun TJ, Bamforth SD, Hoyland D, Phillips HM, et al. Normal and abnormal development of the intrapericardial arterial trunks in humans and mice. Cardiovasc Res. 2012;95:108–15. doi:10.1093/cvr/cvs147.View ArticlePubMedPubMed CentralGoogle Scholar
- Brewer S, Jiang X, Donaldson S, Williams T, Sucov HM. Requirement for AP-2α in cardiac outflow tract morphogenesis. Mech Dev. 2002;110:139–49.View ArticlePubMedGoogle Scholar
- Jiang X, Rowitch DH, Soriano P, McMahon AP, Sucov HM. Fate of the mammalian cardiac neural crest. Development. 2000;127:1607–16.PubMedGoogle Scholar
- Waldo KL, Hutson MR, Ward CC, Zdanowicz M, Stadt HA, Kumiski D, et al. Secondary heart field contributes myocardium and smooth muscle to the arterial pole of the developing heart. Dev Biol. 2005;281:78–90. doi:10.1016/j.ydbio.2005.02.012 View ArticlePubMedGoogle Scholar
- Graham A, Richardson J. Developmental and evolutionary origins of the pharyngeal apparatus. EvoDevo. 2012;3:24. doi:10.1186/2041-9139-3-24.View ArticlePubMedPubMed CentralGoogle Scholar
- Poelman CAC. Note sur systeme circulatoire des Crocodilien. Bull Acad Belg. 1854;21:67–72.Google Scholar
- Le Lièvre CS, Le Douarin NM. Mesenchymal derivatives of the neural crest: analysis of chimaeric quail and chick embryos. J Embryol Exp Morphol. 1975;34:125–54.PubMedGoogle Scholar
- Kirby ML, Gale TF, Stewart DE. Neural crest cells contribute to normal aorticopulmonary septation. Science. 1983;220:1059–61.View ArticlePubMedGoogle Scholar
- Mjaatvedt CH, Nakaoka T, Moreno-Rodriguez R, Norris RA, Kern MJ, Eisenberg CA, et al. The outflow tract of the heart is recruited from a novel heart-forming field. Dev Biol. 2001;238:97–109. doi:10.1006/dbio.2001.0409.View ArticlePubMedGoogle Scholar
- Waldo KL, Kumiski DH, Wallis KT, Stadt HA, Hutson MR, Platt DH, et al. Conotruncal myocardium arises from a secondary heart field. Development. 2001;128:3179–88.PubMedGoogle Scholar
- Kelly RG, Brown NA, Buckingham ME. The arterial pole of the mouse heart forms from Fgf10-expressing cells in pharyngeal mesoderm. Dev Cell. 2001;1:435–40. doi:10.1016/S1534-5807(01)00040-5.View ArticlePubMedGoogle Scholar
- Gittenberger-de Groot AC, Winter EM, Bartelings MM, Goumans MJ, DeRuiter MC, Poelmann RE. The arterial and cardiac epicardium in development, disease and repair. Differentiation. 2012;84:41–53. doi:10.1016/j.diff.2012.05.002.View ArticlePubMedGoogle Scholar
- Pérez-Pomares JM, Phelps A, Sedmerova M, Wessels A. Epicardial-like cells on the distal arterial end of the cardiac outflow tract do not derive from the proepicardium but are derivatives of the cephalic pericardium. Dev Dyn. 2003;227:56–68. doi:10.1002/dvdy.10284.View ArticlePubMedGoogle Scholar
- Poelmann RE, Mikawa T, Gittenberger-de Groot AC. Neural crest cells in outflow tract septation of the embryonic chicken heart: differentiation and apoptosis. Dev Dyn. 1998;212:373–84. doi:10.1002/(SICI)1097-0177(199807)212:3<373:AID-AJA5>3.0.CO;2-E.View ArticlePubMedGoogle Scholar
- Webb S, Qayyum SR, Anderson RH, Lamers WH, Richardson MK. Septation and separation within the outflow tract of the developing heart. J Anat. 2003;202:327–42. doi:10.1046/j.1469-7580.2003.00168.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Harmon AW, Nakano A. Nk2–5 lineage tracing visualizes the distribution of second heart field-derived aortic smooth muscle. Genesis. 2013;51:862–9. doi:10.1002/dvg.22721.View ArticlePubMedPubMed CentralGoogle Scholar
- Poelmann RE, Gittenberger-de Groot AC, Vicente-Steijn R, Wisse LJ, Bartelings MM, Everts S, et al. Evolution and development of ventricular septation in the amniote heart. PLoS ONE. 2014;9:e106569. doi:10.1371/journal.pone.0136025.View ArticlePubMedPubMed CentralGoogle Scholar
- Rathke H. Untersuchungen Ueber die Aortenwurzeln und die von ihnen ausgehenden Arterien der Saurier. Wien: Kaiserlich-Koeniglichen Hof- and Staatdruckerei; 1857. p. 1–94.Google Scholar
- O’Donoghue CH. A note on the ductus caroticus and ductus arteriosus and their distribution in the reptilia. J Anat. 1917;51:137–49.PubMedPubMed CentralGoogle Scholar
- Zug GR. The distribution and patterns of the major arteries of the iguanids and comments on the intergeneric relationships of Iguanids (Reptilia: Lacertilia). Smithson Contr Zool. 1971;83:1–23.View ArticleGoogle Scholar
- Farmer CG. On the evolution of arterial vascular patterns of tetrapods. J Morphol. 2011;272:1325–41. doi:10.1002/jmor.10986.View ArticlePubMedGoogle Scholar
- Molin DG, DeRuiter MC, Wisse LJ, Azhar M, Doetschman T, Poelmann RE, et al. Altered apoptosis pattern during pharyngeal arch artery remodelling is associated with aortic arch malformations in Tgfbeta2 knock-out mice. Cardiovasc Res. 2002;56:312–22. doi:10.1016/S0008-6363(02)00542-4.View ArticlePubMedGoogle Scholar
- Bökenkamp R, van Brempt R, van Munsteren JC, van den Wijngaert I, de Hoogt R, Finos L, Goeman J, et al. Dlx1 and Rgs5 in the ductus arteriosus: vessel-specific genes identified by transcriptional profiling of laser-capture microdissected endothelial and smooth muscle cells. PLoS ONE. 2014;9:e86892. doi:10.1371/journal.pone.0086892.View ArticlePubMedPubMed CentralGoogle Scholar
- Goodrich ES. On the classification of the Reptilian. Proc R Soc B. 1916;89:261–76.View ArticleGoogle Scholar
- Holmes EB. A reconsideration of the phylogeny of the tetrapod heart. J Morph. 1975;147:209–28.View ArticleGoogle Scholar
- Werneburg I, Sánchez-Villagra MR. Timing of organogenesis support basal position of turtles in the amniote tree of life. BMC Evol Biol. 2009;23(9):82. doi:10.1186/1471-2148-9-82.View ArticleGoogle Scholar
- Lyson TR, Sperling EA, Heimberg AM, Gauthier JA, King BL, Peterson KJ. MicroRNAs support a turtle+ lizard clade. Biol Lett. 2012;8:104–7. doi:10.1098/rsbl.2011.0477.View ArticlePubMedGoogle Scholar
- Chiari Y, Cahais V, Galtier N, Delsuc F. Phylogenomic analyses support the position of turtles as the sister group of birds and crocodiles (Archosauria). BMC Biol. 2012;10:65. doi:10.1186/1741-7007-10-65.View ArticlePubMedPubMed CentralGoogle Scholar
- Crawford NG, Faircloth BC, McCormack JE, Brumfield RT, Winker K, Glenn TC. More than 1000 ultraconserved elements provide evidence that turtles are the sister group of archosaurs. Biol Lett. 2012;23(8):783–6. doi:10.1098/rsbl.2012.0331.View ArticleGoogle Scholar
- Shaffer HB, Minx P, Warren DE, Shedlock AM, Thomson RC, Valenzuela N, et al. The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage. Genome Biol. 2013;14:R28. doi:10.1186/gb-2013-14-3-r28.View ArticlePubMedGoogle Scholar
- Wang Z, Pascual-Anaya J, Zadissa A, Li W, Niimura Y, Huang Z, et al. The draft genomes of soft-shell turtle and green sea turtle yield insights into the development and evolution of the turtle-specific body plan. Nat Genet. 2014;2013(45):701–6. doi:10.1038/ng.2615 (Erratum in: Nat Genet. 2014;46:657).Google Scholar
- Green RE, Braun EL, Armstrong J, Earl D, Nguyen N, Hickey G, et al. Three crocodilian genomes reveal ancestral patterns of evolution among archosaurs. Science. 2014;346:1254449. doi:10.1126/science.1254449.View ArticlePubMedPubMed CentralGoogle Scholar
- Hogers B, DeRuiter MC, Baasten AM, Gittenberger-de Groot AC, Poelmann RE. Intracardiac blood flow patterns related to the yolk sac circulation of the chick embryo. Circ Res. 1995;76:871–7. doi:10.1161/01.RES.76.5.871.View ArticlePubMedGoogle Scholar
- Hogers B, DeRuiter MC, Gittenberger-de Groot AC, Poelmann RE. Unilateral vitelline vein ligation alters intracardiac blood flow patterns and morphogenesis in the chick embryo. Circ Res. 1997;80:473–81. doi:10.1161/01.RES.80.4.473.View ArticlePubMedGoogle Scholar
- Hove JR, Köster RW, Forouhar AS, Acevedo-Bolton G, Fraser SE, Gharib M. Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis. Nature. 2003;421:172–7. doi:10.1038/nature01282.View ArticlePubMedGoogle Scholar
- Kowalski WJ, Dur O, Wang Y, Patrick MJ, Tinney JP, Keller BB, et al. Critical transitions in early embryonic aortic arch patterning and hemodynamics. PLoS ONE. 2013;8:e60271. doi:10.1371/journal.pone.0060271.View ArticlePubMedPubMed CentralGoogle Scholar
- Groenendijk BC, Hierck BP, Gittenberger-De Groot AC, Poelmann RE. Development-related changes in the expression of shear stress responsive genes KLF-2, ET-1, and NOS-3 in the developing cardiovascular system of chicken embryos. Dev Dyn. 2004;230:57–68. doi:10.1002/dvdy.20029.View ArticlePubMedGoogle Scholar
- Sanger TJ, Losos JB, Gibson-Brown JJ. A developmental staging series for the lizard genus Anolis: a new system for the integration of evolution, development, and ecology. J Morphol. 2008;269:129–37. doi:10.1002/jmor.10563.View ArticlePubMedGoogle Scholar
- Yntema CL. A series of stages in the embryonic development of Chelydra serpentina. J Morphol. 1968;125:219–51.View ArticlePubMedGoogle Scholar
- Ferguson MWJ. Reproductive embryology and embryology of the crocodilians. In: Gans C, Fillett F, Maderson PFA, editors. Biology of the reptilia. New York: Wiley; 1985. p. 330–491.Google Scholar
- Tokita M, Kuratani S. Normal embryonic stages of the Chinese softshelled turtle Pelodiscus sinensis (Trionychidae). Zool Sci. 2001;18:705–15.View ArticleGoogle Scholar
- Werneburg I. A standard system to study vertebrate embryos. PLoS ONE. 2009;4:e5887. doi:10.1371/journal.pone.0005887.View ArticlePubMedPubMed CentralGoogle Scholar
- Hamburger V, Hamilton HL. A series of normal stages in the development of the chick embryo. J Morphol. 1951;88:49–92.View ArticlePubMedGoogle Scholar
- Richardson MK. Heterochrony and the phylotypic period. Dev Biol. 1995;172:412–21. doi:10.1006/dbio.1995.8041.View ArticlePubMedGoogle Scholar
- Hohenstein P, Hastie ND. The many facets of the Wilms’ tumour gene, WT1. Hum Mol Genet. 2006;15:R196–201. doi:10.1093/hmg/ddl196.View ArticlePubMedGoogle Scholar
- Dong L, Pietsch S, Englert C. Towards an understanding of kidney diseases associated with WT1 mutations. Kidney Int. 2015;88:684–90. doi:10.1038/ki.2015.198.View ArticlePubMedPubMed CentralGoogle Scholar
- López D, Durán AC, de Andrés AV, Guerrero A, Blasco M, Sans-Coma V. Formation of cartilage in the heart of the Spanish terrapin, Mauremys leprosa (Reptilia, Chelonia). J Morphol. 2003;258(1):97–105.View ArticlePubMedGoogle Scholar
- Bertens LM, Richardson MK, Verbeek FJ. Analysis of cardiac development in the turtle Emys orbicularis (Testudines: Emidydae) using 3-D computer modeling from histological sections. Anat Rec. 2010;293:1101–14. doi:10.1002/ar.21162.View ArticleGoogle Scholar
- Wyneken J. Normal reptile heart morphology and function. Vet Clin North Am Exot Anim Pract. 2009;12:51–63, vi. doi:10.1016/j.cvex.2008.08.001.
- Crawford NG, Parham JF, Sellas AB, Faircloth BC, Glenn TC, Papenfuss TJ, et al. A phylogenomic analysis of turtles. Mol Phylogenet Evol. 2015;83:250–7. doi:10.1016/j.ympev.2014.10.021.View ArticlePubMedGoogle Scholar
- Seymour RS, Bennett-Stamper CL, Johnston SD, Carrier DR, Grigg GC. Evidence for endothermic ancestors of crocodiles at the stem of archosaur evolution. Physiol Biochem Zool. 2004;77:1051–67. doi:10.1086/422766.View ArticlePubMedGoogle Scholar
- Grewal N, DeRuiter MC, Jongbloed MR, Goumans MJ, Klautz RJ, Poelmann RE, et al. Normal and abnormal development of the aortic wall and valve: correlation with clinical entities. Neth Heart J. 2014;22:363–9. doi:10.1007/s12471-015-0784-4.View ArticlePubMedPubMed CentralGoogle Scholar
- Abu-Issa R. Heart fields: spatial polarity and temporal dynamics. Anat Rec. 2014;297:175–82. doi:10.1002/ar.22831.View ArticleGoogle Scholar
- Norden J, Grieskamp T, Lausch E, van Wijk B, van den Hoff MJ, Englert C, et al. Wt1 and retinoic acid signaling in the subcoelomic mesenchyme control the development of the pleuropericardial membranes and the sinus horns. Circ Res. 2010;106:1212–20. doi:10.1161/CIRCRESAHA.110.217455.View ArticlePubMedPubMed CentralGoogle Scholar
- Gittenberger-de Groot AC, Calkoen EE, Poelmann RE, Bartelings MM, Jongbloed MR. Morphogenesis and molecular considerations on congenital cardiac septal defects. Ann Med. 2014;46:640–52. doi:10.3109/07853890.2014.959557.View ArticlePubMedGoogle Scholar
- Keyte A, Hutson MR. The neural crest in cardiac congenital anomalies. Differentiation. 2012;84:25–40. doi:10.1016/j.diff.2012.04.005.View ArticlePubMedPubMed CentralGoogle Scholar
- Keyte AL, Alonzo-Johnsen M, Hutson MR. Evolutionary and developmental origins of the cardiac neural crest: building a divided outflow tract. Birth Defects Res C Embryo Today. 2014;102:309–23. doi:10.1002/bdrc.21076.View ArticlePubMedPubMed CentralGoogle Scholar
- White FN. Circulation in the reptilian heart (Caiman sclerops). Anat Rec. 1956;125:417–31.View ArticlePubMedGoogle Scholar
- Axelsson M, Franklin CE, Lofman CO, Nilsson S, Grigg GS. Dynamic anatomical study of cardiac shunting in crocodiles using high-resolution angioscopy. J Exp Biol. 1996;199:359–65.PubMedGoogle Scholar
- High FA, Jain R, Stoller JZ, Antonucci NB, Lu MM, Loomes KM, et al. Murine Jagged1/Notch signaling in the second heart field orchestrates Fgf8 expression and tissue-tissue interactions during outflow tract development. J Clin Investig. 2009;119:1986–96. doi:10.1172/JCI38922.PubMedPubMed CentralGoogle Scholar
- Gittenberger-de Groot AC, Bartelings MM, Poelmann RE, Haak MC, Jongbloed MR. Embryology of the heart and its impact on understanding fetal and neonatal heart disease. Semin Fetal Neonatal Med. 2013;18:237–44. doi:10.1016/j.siny.2013.04.008.View ArticlePubMedGoogle Scholar
- Poelmann RE, Gittenberger-de Groot AC. Apoptosis as an instrument in cardiovascular development. Birth Defects Res C Embryo Today. 2005;75:305–13. doi:10.1002/bdrc.20058.View ArticlePubMedGoogle Scholar
- Keyes WM, Sanders EJ. Regulation of apoptosis in the endocardial cushions of the developing chick heart. Am J Physiol Cell Physiol. 2002;282:C1348–60. doi:10.1152/ajpcell.00509.2001.View ArticlePubMedGoogle Scholar
- Fisher SA, Langille BL, Srivastava D. Apoptosis during cardiovascular development. Circ Res. 2010;87:856–64. doi:10.1161/01.RES.87.10.856.View ArticleGoogle Scholar
- Cooley MA, Kern CB, Fresco VM, Wessels A, Thompson RP, McQuinn TC, et al. Fibulin-1 is required for morphogenesis of neural crest-derived structures. Dev Biol. 2008;319:336–45. doi:10.1016/j.ydbio.2008.04.029.View ArticlePubMedPubMed CentralGoogle Scholar
- Schaefer KS, Doughman YQ, Fisher SA, Watanabe M. Dynamic patterns of apoptosis in the developing chicken heart. Dev Dyn. 2004;229:489–99. doi:10.1002/dvdy.10463.View ArticlePubMedGoogle Scholar
- Eralp I, Lie-Venema H, DeRuiter MC, van den Akker NM, Bogers AJ, Mentink MMT, et al. Coronary artery and orifice development is associated with proper timing of epicardial outgrowth and correlated Fas-ligand-associated apoptosis patterns. Circ Res. 2005;8(96):526–34. doi:10.1161/01.RES.0000158965.34647.4e.View ArticleGoogle Scholar
- Winokur RM. Adaptive modifications of buccal mucosae in turtles. Am Zool. 1973;13:1347–8.Google Scholar
- Ernst CH, Lovich JE. Turtles of the United States and Canada. 2nd ed. Baltimore: Johns Hopkins University Press; 2009. p. 641.Google Scholar
- Ip YK, Loong AM, Lee SM, Ong JL, Wong WP, Chew SF. The Chinese soft-shelled turtle, Pelodiscus sinensis, excretes urea mainly through the mouth instead of the kidney. J Exp Biol. 2012;215:3723–33. doi:10.1242/jeb.068916.View ArticlePubMedGoogle Scholar
- Poelmann RE, Gittenberger-de Groot AC, Mentink MM, Bökenkamp R, Hogers B. Development of the cardiac coronary vascular endothelium, studied with antiendothelial antibodies, in chicken-quail chimeras. Circ Res. 1993;73:559–68. doi:10.1161/01.RES.73.3.559.View ArticlePubMedGoogle Scholar
- Red-Horse K, Ueno H, Weissman IL, Krasnow MA. Coronary arteries form by developmental reprogramming of venous cells. Nature. 2010;464:549–53. doi:10.1038/nature08873.View ArticlePubMedPubMed CentralGoogle Scholar
- Bogers AJ, Gittenberger-de Groot AC, Poelmann RE, Péault BM, Huysmans A. Development of the origin of the coronary arteries, a matter of ingrowth or outgrowth? Anat Embryol. 1989;180:437–41.View ArticlePubMedGoogle Scholar
- Tian X, Hu T, He L, Zhang H, Huang X, Poelmann RE, et al. Peritruncal coronary endothelial cells contribute to proximal coronary artery stems and their aortic orifices in the mouse heart. PLoS ONE. 2013;8:e80857. doi:10.1371/journal.pone.0080857.View ArticlePubMedPubMed CentralGoogle Scholar
- Théveniau-Ruissy M, Pérez-Pomares JM, Parisot P, Baldini A, Miquerol L, Kelly RG. Coronary stem development in wild-type and Tbx1 null mouse hearts. Dev Dyn. 2016;245:445–59. doi:10.1002/dvdy.24380.View ArticlePubMedGoogle Scholar
- Jensen B, Moorman AF, Wang T. Structure and function of the hearts of lizards and snakes. Biol Rev Camb Philos Soc. 2014;89:302–36. doi:10.1111/brv.12056.View ArticlePubMedGoogle Scholar