Development and epithelial organisation of muscle cells in the sea anemone Nematostella vectensis
© Jahnel et al.; licensee BioMed Central Ltd. 2014
Received: 11 April 2014
Accepted: 14 June 2014
Published: 18 June 2014
Nematostella vectensis, a member of the cnidarian class Anthozoa, has been established as a promising model system in developmental biology, but while information about the genetic regulation of embryonic development is rapidly increasing, little is known about the cellular organization of the various cell types in the adult. Here, we studied the anatomy and development of the muscular system of N. vectensis to obtain further insights into the evolution of muscle cells.
The muscular system of N. vectensis is comprised of five distinct muscle groups, which are differentiated into a tentacle and a body column system. Both systems house longitudinal as well as circular portions. With the exception of the ectodermal tentacle longitudinal muscle, all muscle groups are of endodermal origin. The shape and epithelial organization of muscle cells vary considerably between different muscle groups. Ring muscle cells are formed as epitheliomuscular cells in which the myofilaments are housed in the basal part of the cell, while the apical part is connected to neighboring cells by apical cell-cell junctions. In the longitudinal muscles of the column, the muscular part at the basal side is connected to the apical part by a long and narrow cytoplasmic bridge. The organization of these cells, however, remains epitheliomuscular. A third type of muscle cell is represented in the longitudinal muscle of the tentacle. Using transgenic animals we show that the apical cell-cell junctions are lost during differentiation, resulting in a detachment of the muscle cells to a basiepithelial position. These muscle cells are still located within the epithelium and outside of the basal matrix, therefore constituting basiepithelial myocytes. We demonstrate that all muscle cells, including the longitudinal basiepithelial muscle cells of the tentacle, initially differentiate from regular epithelial cells before they alter their epithelial organisation.
A wide range of different muscle cell morphologies can already be found in a single animal. This suggests how a transition from an epithelially organized muscle system to a mesenchymal could have occurred. Our study on N. vectensis provides new insights into the organisation of a muscle system in a non-bilaterian organism.
Muscles are present in all metazoans except sponges and placozoans. Their emergence marks an important step in evolution because it allows organisms to disperse, escape, hunt and explore new habitats. Muscle cells are a major derivative of the mesoderm in Bilateria, but can also be found in two non-bilaterian phyla, the Ctenophora and the Cnidaria. The diploblastic Cnidaria are of particular interest for understanding the evolution of key bilaterian traits because, they are considered to be the sister group of the Bilateria [1, 2] and therefore occupy a crucial phylogenetic position. Cnidarian polyps generally have smooth muscles, yet medusae also have striated muscles . The striking structural similarity of striated muscles in Cnidaria and Bilateria has led to the suggestion that striated muscles of Cnidaria and Bilateria are homologous . These authors extended their arguments by proposing that cnidarians are reduced Mesodermata . However, a recent phylogenomic study tracing the evolutionary origin of all muscle components known from model bilaterians revealed the absence of several crucial muscle proteins from the genome of non-bilaterian organisms as well as the bilaterian lineage-specific innovations of other crucial muscle proteins . These phylogenetic and expression analyses led to the conclusion that striated muscles evolved convergently in cnidarians and bilaterians, on the basis of ancestral proteins, which predate the divergence of animals . Furthermore, several key myogenic transcription factors such as MyoD and MRFs (myogenic regulatory factors) have not been identified in cnidarians. This raises questions of how muscles in cnidarians develop and how they are structured.
In recent years, N. vectensis, a representative of the Anthozoa, has been established as an important model for studying embryology, phylogenetic relationships, comparative genomics and the origin of triploblasty [6–8]. This makes it a promising addition to the existing group of cnidarian model systems. Gene expression and functional studies have led to a much better understanding of the molecular regulation of embryogenesis and larval development during the last decade. Nonetheless, our knowledge about the anatomy and cellular composition of this new model organism remains poor. Often, not even the cell types that account for a highly specific gene expression pattern are known. In particular, the adult stage is poorly understood. Hence, as N. vectensis continues to develop into a major cnidarian model organism, we need to reach a deeper understanding of the composition, connections and differentiation kinetics of the different cell types at various developmental stages.
Frank and Bleakney  investigated the general anatomy of N. vectensis at a histological level, yet the level of resolution and the detail of analysis did not enable conclusions to be drawn about the development and precise cellular composition of the various cell types.
Here, we present a detailed anatomical description of the muscular system of N. vectensis using histology, electron microscopy, confocal microscopy and transgenic lines, specifically expressing reporter genes in retractor muscles of the column and tentacles. We show that muscle cells display different levels of epithelial organization, dependent on their position in the organism. They vary from an epitheliomuscular organisation to a basiepithelial muscle cell, which has lost all apical cell-cell junctions and subsequently is positioned at the base of the epithelium. Our data suggest that epitheliomuscular cells can be highly modified to comply with spatial constraints. Based on these results we interpret the different modes of epithelialization to represent intermediate steps of detachment from the epithelium, which finally would enable muscle cells to become located between the ectoderm and endoderm.
Animals were cultured and spawning was induced as described elsewhere [10, 11]. In brief, animals were kept at 18°C, predominantly in the dark, and spawning was induced by raising the temperature to 24°C in the presence of light for 10 h.
Adult animals were anesthetized with a few drops of 7% MgCl2 for 30 min and fixed in 4% PFA (paraformaldehyde) in PBT (phosphate buffered saline, 0.2% Triton) overnight, washed in PBT, dehydrated in ethanol and methyl benzoate and embedded in paraffin. Sections (7 μm) were stained with Azan.
Transmission electron microscopy
Samples were put on ice and anesthetized as described above with MgCl2 (primary polyps, adults) and subsequently fixed with 2.5% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.2) for 1 h (planulae, primary polyps) or overnight (adults) at 4°C. After fixation, samples were either stored in 1.25% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.2) at 4°C or processed immediately. Then they were washed in the same buffer used for fixation. Samples were postfixed in 1% OsO4 in 0.1 M cacodylate buffer (pH 7.2) for 30 min and washed with 0.1 M cacodylate buffer (pH 7.2). Thereafter they were dehydrated through a graded series of ethanol and acetone and embedded into the Low Viscosity Resin (Agar) following sectioning using routine techniques. After staining with watery solutions of uranylacetate (20 min) and lead citrate (10 min), sections were examined with a Zeiss Libra 120 transmission electron microscope.
Animals were anesthetized as described above and fixed in 4% PFA in PBT overnight at 4°C and subsequently washed in the same buffer. Permeabilization was enhanced by putting embryos into ice-cold (−20°C) acetone for 7 min followed by thoroughly washing in PBT. Subsequently samples were incubated in Phalloidin-Alexa 488 (Invitrogen) (3 μl/100 μl PBT) for at least overnight at 4°C in the dark, washed in PBT and mounted on glass slides in Vectashield.
Stained animals were cut into smaller pieces and incubated in OCT infiltration solution (20% OCT compound (Sakura), 25% sucrose in PBS) overnight, followed by putting them in a drop of 80% OCT (80% OCT, 25% sucrose in PBS) on a glass slide. A plastic mold was placed over them and filled with two additional drops of 80% OCT. After orientation the slide was placed on a metal block (precooled in liquid nitrogen) and immediately filled with 100% OCT. The solid frozen samples were stored at −20°C or processed immediately. Sections (14 μm) were cut in a Leica CM3050S cryostat at −24°C and collected on warm (RT) Superfrost Ultra Plus slides (Thermo Scientific). After a drying step (RT, overnight in the dark) the slides were placed in PBS for 5 min to wash away the embedding medium and mounted immediately in Vectashield.
Samples were anesthetized (primary polyps) and fixed in 4% PFA in PBT for 6 h, washed in PBT and blocked in blocking buffer (80% PBT, 20% sheep serum, 1% bovine serum albuminum) for 2 h at room temperature. They were then incubated in primary antibody (rat, anti-RFP; Chromotek) 1:400 in blocking buffer overnight at 4°C, subsequently washed in PBT and incubated in secondary antibody (goat, anti-rat, DyLight 549; Jackson) 1:500 in blocking buffer containing phalloidin (3 μl/100 μl) for 3 h at room temperature. After an additional washing step, samples were mounted on glass slides in Vectashield.
The body column and its muscles
Cross-sections of adult polyps revealed the presence of eight uniformly constructed mesenteries, each of which extends from the body wall to the actinopharynx. The typical architecture of a fully differentiated mesentery below the pharynx is shown (Figure 2A, Figure 3A). A characteristic bilateral rosette-like folding of the mesoglea is present at the base of each mesentery. These foldings are aligned by the myonemes of the parietal muscle cells (Figure 2B, Figure 3B). These myonemes connect directly to the neighboring ring muscle at the base of the mesentery (Figure 2D, Figure 3B) of the body column at both sides of the mesentery. Towards the distal part of the mesentery, the parietal muscle is separated from the retractor muscle by the stalk. In the retractor muscle the extensive folding of the mesoglea is even more pronounced and branched than in the parietal muscle, but it is formed only on one side (Figure 2C, Figure 3C). The side of the retractor muscle within the mesentery is non-random and defines the directive axis. Between the mesenterial filament (also termed septal filament) at the tip and the retractor muscle, a gametogenic region containing either eggs or sperm – directly embedded within the mesoglea – is present in sexually mature animals.Both parietal and retractor muscle are longitudinal muscles, with the former showing a more complex branching (secondary branching) of the mesoglea (Figure 2C, Figure 3C, Figure 4A); this increases the surface and enables more muscle cells to attach. As a result the overall surface area of myonemes is generally larger in the retractor than in the parietal muscle. In the ring muscle of the body wall the myonemes are arranged perpendicular to the oral-aboral axis. Instead of being a contiguous ring of muscle cells, it consists of eight portions situated between the mesenteries and merging directly into the parietal muscle to each side (Figure 2D, Figure 3B).
Parietal and retractor muscles retain an epithelial organization
In cross-sections of the adult polyp, the cells of the retractor muscle are strongly entangled, making it difficult to follow each cell border from the base to the apex. At the proximal (towards the parietal muscle) and the distal border (towards the mesenterial filament) of the retractor muscle, the myonemes are closer to the apex of the epithelium. Here, a clear continuity can be observed, and the apical part of the cell contributes in building up the epithelium. Via thin cytoplasmic bridges, the apical part is connected to the robust basal, myofilament-containing part, which lies adjacent to the mesoglea (Figure 4E, F). The myonemes are large and well pronounced in the central region of the retractor muscle sheet (Figure 4G). Although not visible in single sections, these myonemes probably also still exhibit a connection to the epithelium. This interpretation is based on the fact that the space between the folded sheet of myonemes is filled with numerous cytoplasmic bridges, all of which originate from single myonemes running towards the apex of the epithelium. The myonemes are connected to each other by spot-like adherens junctions (Figure 4G) and are anchored to the mesoglea by focal adhesion sites (Figure 4E inlet).Likewise, the parietal muscle consists of a serial arrangement of myonemes (Figure 4B). The folding of the muscle sheets is less complex in this region, making it easier to follow individual cells from the base to the apex on single sections. Similar to the retractor muscle, the apical part of the cell in the parietal muscle is connected to neighboring cells to form an epithelium; the myonemes are connected to the apical part by cytoplasmic bridges (Figure 4D). A prominent neural plexus is situated on both sides of the parietal muscle; neurites run mainly along the oral-aboral axis (Figure 4C). The myonemes are again anchored by adherens junctions to neighboring cells and by focal adhesion sites to the mesoglea (Figure 4C, inlet 1).Ring muscle cells are oriented perpendicular to the longitudinal muscles. They span the body wall gastrodermis (adult endoderm) between the parietal muscle portions of all eight mesenteries and show a clear integration into the epithelium, having their myofilaments located at their bases (Figure 4H). In brief, all three muscle types of the body column show an epithelial organisation, but the retractor and parietal muscles are highly modified.
The tentacle muscle system consists of basiepithelial myocytes and epitheliomuscular cells
Tentacles are basically tube-like expansions of the body column at the oral pole with continuation of the gastric cavity (Figure 1). Therefore they are structured in the same way as the double-layered body column, lacking any endodermal invaginations such as mesenteries in the body column (Figure 5A). Most of the cell types present in the tentacles are situated in the epidermis (adult ectoderm), making it most important for the functions of the tentacle. At least two different types of gland cells are present, one with electron-dense and one with electron-light vesicles. One of which has recently been shown to secrete a toxin . Since the main function of the tentacle is to capture prey, it is unsurprising that it is very rich in spirocysts. The longitudinal muscle consists of a discontinuous sheet of myonemes located at the base of the epidermis, forming a ring around the mesoglea. A prominent neural plexus lies on top of that muscle layer; it also shows a ring-like structure (Figure 5B). To clarify whether the basally located myonemes exhibit a connection to the apex of the epithelium, as is the case in the columnar muscles, we produced serial longitudinal- and cross-sections of tentacles. We found that the nuclei of the muscle cells are located near the myofilaments and that no cytoplasmic bridges between the basal myonemes and the apical part of the epithelium are formed. The elongated muscle cells are arranged side by side, connected laterally by spot-like adherens junctions (Figure 5C + D). Through the discontinuous sheet of muscle cells, overlying epithelial cells send their processes and attach to the mesoglea (Figure 5C + F).The gastrodermis of the tentacle is mainly composed of circular muscle cells. They resemble the circular muscles of the body column in that their myofilaments are located basally and in that the connection between the apex and the base of their cells is not drawn into long and thin cytoplasmic bridges. Due to the low myofilament density, the tentacle ring muscle is comparatively weakly developed (Figure 5E).
Development of columnar longitudinal muscles
To investigate the development of columnar longitudinal muscles, subpharyngeal cross-sections of different stages ranging from mid-planula to juvenile polyps were produced. Columnar longitudinal muscles are located in the mesentery, which corresponds to a folding of the endodermal epithelium. The first pair of mesenteries becomes visible on a macroscopic level at the primary polyp stage. They are called primary mesenteries and can be easily distinguished from the remaining three pairs of secondary mesenteries because of their early-formed mesenterial filaments at the distal tip. By comparison the secondary mesenteries form their mesenterial filaments only later during polyp growth. However, when reaching adulthood, all eight mesenteries have developed to a similar degree and they cannot be distinguished anymore on a macroscopic level.Needless to say, a mesenterial anlage is required before muscle cells can develop. A first morphological indication of muscle differentiation was observed in the primary mesenteries of the mid-planula stage (Figure 6A-C). The base of the mesentery (future parietal muscle site) lacks any clear signs of muscle cells (Figure 6B). At the same time, a few cells containing a small number of myofilaments were already visible along the mesentery, lying adjacently to the mesoglea (Figure 6C, inlet). Secondary mesenteries at this stage have not developed any morphologically visible muscular structures yet (data not shown). In late planula stages (Figure 6D-I) the future muscle regions become apparent. The retractor muscle cells of the primary mesenteries have formed additional myofilaments and are positioned side by side (Figure 6E). They emerge slightly distal of the mesentery base, already formed exclusively on one side of the mesentery. At this stage, no clear myofilament formation is visible at the base of the mesentery (Figure 6F). In secondary mesenteries, both muscle groups – parietal and retractor muscles – are identifiable. Unlike the situation in primary mesenteries, here the retractor muscle cells form at the tip of the mesentery, without any bias to one side yet (Figure 6G-I). Generally, muscle cells do not differentiate synchronously in all eight mesenteries. This process is usually quite variable, and neither primary, nor secondary mesenteries are distinctly ahead in the differentiation of muscle cells.In early primary polyps the morphology has changed noticeably. The body wall endoderm has become thinner and the secondary mesenteries are easier visible within the endoderm. The primary mesenteries no longer lie opposite each other and become clearly shifted to one side (Figure 7A). In the retractor- and parietal muscle region of primary and secondary mesenteries, the number of cells with myofilaments increases. At this stage the formation of a neural plexus next to the parietal muscle begins (Figure 7B). In contrast to the parietal muscle, retractor muscle cells of the primary mesenteries already start to constrict the myoneme from the rest of the cell, and cytoplasmic bridges become visible (Figure 7C). In secondary mesenteries (Figure 7D-F), myonemes of the retractor muscle are still located at the tip, but they are already more pronounced on one side of the mesentery (Figure 7F).In the juvenile polyp (Figure 7G-I) the relative position of the primary to the secondary mesenteries becomes clear (although already set in the early planula). The primary mesentery at this stage is composed of a distal mesenterial filament and a proximally located bulged tissue (extending from the stalk to the mesenterial filament) harbouring the retractor muscle at its base. In one of the six secondary mesenteries the mesenterial filament has started to form at the tip; in the remaining ones the retractor muscle is still the most distal structure (Figure 7G). In fully differentiated polyps the secondary mesenteries will have grown to the same size as the primary ones; then, the origin of every single mesentery can only be reconstructed by determining the position of the retractor muscles. The morphology of the parietal muscle resembles that of early stages with the exception that more cells are involved in building up the muscle sheet and that the myonemes become increasingly constricted from the apical epithelial part. The basal part maintains a connection to the apical one and neighboring muscle cells are anchored to each other by adherens junctions at their basal sides. In comparison to the situation in adults (Figure 2B, Figure 3B) the muscle sheets have not folded yet (Figure 7H). The myonemes of the retractor muscle are more densely packed with myofilaments than in the parietal muscle and the cytoplasmic bridge between the base and apex of the cell is already constricted. Like in the parietal muscle, the myonemes are connected to each other by adherens junctions. The muscle sheet is no longer arranged in a straight way, but has started to produce the first folding (Figure 7I). This process will proceed during the maturation of the juvenile, ultimately yielding the typically multiple-folded, one-sided muscle “flag”.The orientation of the retractor muscles leads to an internal bilateral symmetry and is consistent within different individuals. Primary mesenteries always have a predetermined place in this system. This makes it possible to predict the site of retractor muscle formation as soon as the mesenteries have set and before there are any morphological signs of muscle cell differentiation (Figure 7J).Staining with phalloidin additionally demonstrated the accumulation of F-actin in presumptive muscle cells during the development from the planula to the primary polyp. Endodermally located F-actin is already present in the early planula but does not yet show a clear concentration and uniform orientation (Figure 8A, D, G). In the late planula those actin threads become increasingly concentrated and exhibit a clear orientation along the oral-aboral axis. In the future tentacle bulb region, single cells have accumulated F-actin in their basal part (Figure 8B, E, H). In the early primary polyp an increasing number of future tentacle cells show concentrated F-actin; the columnar muscles already are differentiated into a parietal- and a retractor muscle region (Figure 8C, F, I).
Development of tentacle longitudinal muscles
As mentioned above, fully differentiated longitudinal muscle cells of the tentacle are situated at the base of the epidermis and show no connection to the apex of the epithelium. In order to determine whether they emerge from originally epithelial cells, we used a transgenic line (MHC::mCherry) that expresses a fluorescent reporter gene (mCherry) under the control of a muscle-specific promotor (striated-myhc, formerly myhc1) specifically in retractor and tentacle muscles . Expression of mCherry was first detected in 4 day mid-planula stages (Figure 9A-G). It starts with several single columnar cells at the oral pole close to the pharynx, spanning the whole thickness of the ectodermal epithelium. Small accumulations of actin filaments are already co-localized with the expression of mCherry in those cells (Figure 9B-D). At this stage most tentacle muscle cells have already abandoned their apical cell contacts and have sunken down to a basiepithelial position. At this stage of cellular differentiation their concentrated F-actin has increased (Figure 9E-G). Although most of the mCherry positive cells are already situated at the base, a few epithelial muscle cells may be present in early primary polyps. Many cells already formed spindle shaped, apical-basal orientated actin-filament accumulations at their bases before mCherry can be detected (Figure 9I-K). The expression of mCherry in the retractor muscle starts in the late planula (data not shown) and becomes more apparent in early primary polyps. In the latter, the nuclei and remaining cell bodies are visibly located on top of the actin-enriched contractile elements (Figure 9L-N). In older primary polyps (13d) the tentacle bulbs have started to grow out and thin actin-filaments have become aligned along the longitudinal axis of the tentacle (Figure 9O-Q). In comparison to earlier stages (7d) the orientation of actin-filaments has shifted by 90° from a basal-apical to a lateral character (Figure 9Q). Correspondingly, the muscle cells become spindle-shaped and oriented along the longitudinal axis of the tentacle, having lost their connection to the apical surface of the epithelium (Figure 9P).
The three types of muscle cell formation presented here are interpreted to be a direct consequence of biomechanical constraints. Ring muscle cells are exclusively situated in the gastrodermis of either the column or tentacles. Beyond their function as contractile units they mainly serve to build up the epithelium. Ring muscle cells are the predominant cell type of that region. The epithelium is relatively flat and a long and thin cytoplasmic bridge is mechanically not necessary to maintain a connection between the base and the apex. In the longitudinal muscles of the column (parietal and retractor muscle) the situation is different. In both muscles the basally situated muscle sheet is pleated accordion-fashioned, enabling more myonemes to attach to the mesoglea; this increases the contractile strength per area . As a result the surface area of the basal side of the epithelium considerably exceeds that of the apex. This requires modifying the interconnecting part if integration into the epithelium is to be maintained. This is exactly what we observed when examining the elongated and slim cytoplasmic bridges: they become progressively apparent when the muscle sheets start to fold.
Unlike in the column, longitudinal muscle cells of the tentacles are located in the epidermis. Tentacles serve to catch prey and are therefore rich in epidermal cell types such as gland cells and nematocytes, which facilitate this function. All cell types are more or less equally distributed in a ring-like manner around the mesoglea. This would leave less space for epitheliomuscular cells. For this reason we interpret the muscle cells to have lost their apical cell-cell junctions to acquire a basiepithelial position. As they have lost their apical cell junctions, the overlying cells must assume the role of building an epithelial barrier. In addition overlying cells require an anchoring to the mesoglea: this is now provided because the muscle layer is no longer continuous.
Comparison of muscle cell types within Cnidaria
Different groups within the Cnidaria show a very high variability in terms of how and where contractile cells are formed. In hydropolyps the muscular system is exclusively composed of smooth epitheliomuscular cells. While longitudinally orientated myonemes are located in the epidermis, circularly arranged myonemes are located in the gastrodermis. Both epithelia mainly consist of epitheliomuscular cells . In the hydromedusa of Obelia the ectodermal subumbrella is composed of epitheliomuscular cells with both radial helical myofibrils and submerged myocytes, which exhibit true striation . In scyphopolyps the muscular system is exclusively formed by the ectoderm. Here the different muscle fields are physically continuous at the peristomial pits and are either epitheliomuscular (tentacle) or formed as myocytes (column) embedded within the mesoglea. Myofibrills are striated at least in some parts of the polyp before they merge into smooth fibers . The muscle cells of Scyphomedusae are located in the ectodermal subumbrella and formed as circular striated and radial smooth epitheliomuscular cells [18, 19]. Werner and colleagues have shown that the muscular system in cubopolyps mainly consists of ectodermal muscle cells . They are either composed of myocytes, which are embedded into the mesoglea (Carybdea), or of myocytes and additional epitheliomuscular cells (Tripedalia). With the exception of the tentacle tips, all muscle cells have smooth fibers. In Cubomedusae, muscles are subumbrellar (ectodermal) and epitheliomuscular with circular, striated fibers that turn radially in the frenulae of the velarium [21, 3]. From anthozoan polyps, predominantly smooth and epitheliomuscular cells have been reported. Striated muscle fibers, however, have been found in a small subset of actiniarian anthozoans . Hyman  and Muscatine & Lenhoff  report the existence of additional epidermal muscle cells that are independent from the supporting cells and have adopted a subepidermal position. The latter descriptions are not consistent with our findings because we demonstrate the myocyte-nature of longitudinal tentacle cells: they take on a basiepithelial position, connected on the basal side to the mesoglea. In fact they represent basiepithelial myocytes.
Origin, striation and cellular organization of cnidarian muscles
In general, cnidarian tissues show a low grade of division of labor . It has been hypothesized that multifunctionality is a general feature of ancient cell types and that during the course of evolution these multiple functions were segregated among sister cell types. A case in point is epitheliomuscular cells . Our observations support this hypothesis, as we were able to observe the process of de-epithelialization of initially epithelial muscle cells to a basiepithelial location in a single animal. In contrast, a comprehensive comparative analysis of the evolutionary origin of all known muscle proteins revealed that many components are either very ancient, pre-dating the origin of animals, or they evolved rather late in specific lineages . No molecular synapomorphy has been found that would explain the emergence of striated muscles. This suggests that striated muscles have evolved independently in cnidarians, ctenophores and bilaterians, using a core set of ancient muscle proteins .
Cnidaria are still thought to exhibit the most primitive state of an interconnected muscular system . The fact that both epitheliomuscular cells and myocytes are present in all cnidarian classes indicates that they must have already been present in the last common ancestor of Cnidaria and Bilateria. While in Cnidaria epitheliomuscular cells still play a major role in building up a contractile apparatus, this function is progressively adopted by mesodermal myocytes in Bilateria. Clearly, the evolution of mesoderm constitutes a crucial step in facilitating the emergence of complex muscular systems. Myocytes themselves, however, might have played a vital role in the early evolution of mesoderm. Nemertodermatid and acoel myocytes, like other mesodermal cells, apparently originate from the gastrodermis before they eventually emigrate into a subepithelial position . A continuous sequence from epitheliomuscular cells to a subperitoneal musculature has been discovered in annelids and echinoderms, suggesting the epithelial organization of mesodermal muscle cells is an ancestral state [25–30].
In this context N. vectensis might represent an additional model for demonstrating the early stage of emigration of epitheliomuscular cells. N. vectensis myocytes have not been observed to entirely detach from the epithelium and to result in a mesenchymal, subepithelial position. Nonetheless, one can easily envisage such a process, which would ultimately lead to the situation in cubo- and scyphopolyps, where certain myocytes are completely embedded in the mesoglea [20, 17].
We thank the Core Facility Cell Imaging and Ultrastructure Research of the Faculty of Life Sciences for support with the confocal and electron microscopy. We are grateful to Michael Stachowitsch for critically reading the manuscript. This work was supported by the Austrian Science Fund (FWF) grant (P21108-B17) to U.T.
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