Structure of the central nervous system of a juvenile acoel, Symsagittifera roscoffensis
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The neuroarchitecture of Acoela has been at the center of morphological debates. Some authors, using immunochemical tools, suggest that the nervous system in Acoela is organized as a commissural brain that bears little resemblance to the central, ganglionic type brain of other flatworms, and bilaterians in general. Others, who used histological staining on paraffin sections, conclude that it is a compact structure (an endonal brain; e.g., Raikova 2004; von Graff 1891; Delage Arch Zool Exp Gén 4:109-144, 1886). To address this question with modern tools, we have obtained images from serial transmission electron microscopic sections of the entire hatchling of Symsagittifera roscoffensis. In addition, we obtained data from wholemounts of hatchlings labeled with markers for serotonin and tyrosinated tubulin. Our data show that the central nervous system of a juvenile S. roscoffensis consists of an anterior compact brain, formed by a dense, bilobed mass of neuronal cell bodies surrounding a central neuropile. The neuropile flanks the median statocyst and contains several types of neurites, classified according to their types of synaptic vesicles. The neuropile issues three pairs of nerve cords that run at different dorso-ventral positions along the whole length of the body. Neuronal cell bodies flank the cords, and neuromuscular synapses are abundant. The TEM analysis also reveals different classes of peripheral sensory neurons and provides valuable information about the spatial relationships between neurites and other cell types within the brain and nerve cords. We conclude that the acoel S. roscoffensis has a central brain that is comparable in size and architecture to the brain of other (rhabditophoran) flatworms.
KeywordsAcoel Central nervous system Nerve cords Nerve net Sensory receptors Transmission electronic microscopy 3D modeling software
Acoela are small aquatic (mostly marine) worms characterized by the absence of body cavities, a proper gut, protonephridia, and oviducts. (von Graff 1891; Bresslau 1909; Hyman 1951; Bush 1981; Rieger et al. 1991; Hooge and Tyler 2003; Achatz 2005). Morphological studies based on the male copulatory organ, the sperm structure, and the body wall musculature (Hooge 2001; Kostenko and Mankaev 1990) have distinguished 21 families and about 380 species (Hooge and Tyler 2006) to date. Traditionally, Acoela were placed among the Platyhelminthes, but recent molecular phylogenetic studies suggest that this taxon is the sister group of the remaining bilaterians (Ruiz-Trillo et al. 1999, 2004; Halanych 2004; Sempere et al. 2007; Wallberg et al. 2007; Philippe et al. 2007; Hejnol et al. 2009). In addition, according to some authors, morphological studies using characters such as ciliary rootlets, epidermis, and brain, also favor the separation of the Acoela from the remainder of the platyhelminthes (“Rhabditophora”) and place the Acoela as the first offshot of the bilaterian animals (Haszprunar 1996; Kotikova and Raikova 2008).
If Acoela are the earliest member of Bilateria, this placement would have profound implications for the theory of bilaterian origins (Salvini-Plawen 1978; Holland 2003; Baguñà and Riutort 2004; Hejnol and Martindale 2008). This scenario, in fact, suggests the possibility that the common bilaterian ancestor might have had the structural complexity of a modern acoel, underlining the importance of understanding in detail the structural and functional characteristics of the acoel bauplan. In this paper we present the results of our analysis of the nervous system of the acoel Symsagittifera roscoffensis.
The nervous system of Acoela has so far been studied mainly by immuno-histochemical methods (i.e., antibodies against different neurotransmitters; Raikova 2004; Reuter et al. 1998; Kotikova and Raikova 2008; Gaerber et al. 2007), and ultrastructural approaches (Reisinger 1925; Ramachandra et al. 2000; Tyler 2001). Based on the immuno-histochemical markers (in particular, the expression of the transmitter serotonin), Raikova (2004) claimed that the central nervous system (CNS) of Acoela is a commissural brain (i.e., a regular pattern of longitudinal nerve cords interconnected by transversal commissures). However, it is important to point out that such markers reveal only a very limited set of neurons, leaving a significant part of the nervous system unlabeled (Cebrià 2008; Grimmelikhuijzen et al. 2002). Using a different set of approaches involving the analysis of histological material and electron microscopy, other authors have demonstrated the presence of a central brain surrounding the statocyst in this group of animals (von Graff 1891; Delage 1886; Reisinger 1925; Ramachandra et al. 2000; Tyler 2001). In a detailed analysis, Delage (1886) showed that the CNS in adult and juvenile Convoluta (Symsagittifera) schultzii (Acoela, Sagittiferidae) appears to be formed by a bilobed mass of neuronal bodies with commissure and connective complexes. More recently, with the help of transmission electron microscopy, it has been possible to obtain a more detailed view of the constituent cells in two acoel species, Convoluta (Symsagittifera) psammophila and Otocelis rubropunctata (Acoela, Oticelididae) (Bedini and Lanfranchi 1991).
In spite of the use of different histological tools, it has been impossible to define so far, with cellular resolution, the fine structure of any acoel nervous system. To tackle this problem, we have started to undertake a thorough investigation of the nervous system of the S. roscoffensis hatchling. We use this species as an experimental system due to the fact that we have access to all developmental stages throughout much of the year (Keeble 1910). The use of antibody markers and of serial transmission electron microscopy sections of the complete animal, plus new 3D modeling software (TrakEM2) reveals that S. roscoffensis (and probably most acoels) have a brain containing a “central mass” of neurons that gives rise to three pairs of nerve cords that extend along the whole body length. We here provide a first description of ultrastructural details of the brain, nerve cords and peripheral nervous system of S. roscoffensis.
Materials and methods
Egg clusters were obtained from cultures of adult specimens collected in Brittany (France), near the Station Biologique de Roscoff. They were shipped to Barcelona and then stored at 15°C in plastic dishes filled with artificial seawater (ASW). ASW salinity was adjusted to the levels of the seawater around Roscoff. 50-W fluorescent tubes provided illumination and the animals were kept in a cycle of 12 h light and 12 h darkness in an environmental chamber, model SANYO MLR-350. Hatchlings were less than 3 days old when fixed. All hatchlings used in this paper were collected in 2006 and 2007.
Anti-acetyl tyrosine tubulin
The antibody reacts against tubulin’s C-terminal tyrosine, an epitope that is present in many metazoan neurons and cilia. The ubiquity of this epitope allows detecting more neuron than when using any other neuronal marker.
Specimens were fixed in 4% paraformaldehyde (PFA) (made in 1× phosphate-buffered saline; PBS) for 1 h at 4°C. After several washes in 1× PBS, they were stored in a solution of 1× PBS, 0.1% sodium acid at 4°C until use. After one wash in 1× PBS/0.1%TritonX-100 (PBT), specimens were blocked in 3%NGS/PBT for 1 h at room temperature (RT). Then they were incubated with a mouse anti-acetyl tyrosine tubulin (anti-TyrTub) antiserum (Sigma), at 1:100 dilution overnight at 4°C. Then specimens were washed several times in PBT and blocked in 3%NGS/PBT for 1 h at RT. Thereafter, specimens were incubated for 2 h with the secondary antibody, fluorescein isothiocyanate (FITC)-labeled anti-mouse immunoserum (Sigma; dilution 1:100). Finally, and after several washes in PBS, specimens were mounted in Vectashield media (Vector) and examined with an inverted confocal SPII Leica microscope. Image analysis was carried out using the software package: Leica Confocal Software.
Some samples were contrasted with phalloidin after the anti-TyrTub immunochemistry. Staining with Alexa Fluor 568-phalloidin (Molecular Probes, dilution 1:70) was performed for 1 h at RT. Following the removal of the phalloidin solution and two washes in 1× PBS, staining of cell nuclei was carried out by incubating the samples in DAPI (4′, 6-diamino-phenyin-dole, dilactate; Sigma-Aldrich, Steinheim, Germany).
This antibody specifically recognizes a monoamine neurotransmitter (5-hydroxytryptamine, or 5-HT) that is synthesized in serotonergic neurons. The anti-5-HT staining method has been widely used to reveal the overall structure of the nervous system in Acoela (Raikova 2004). Specimens were fixed in 4% PFA (made in 1× PBS) for 1 h at 4°C. After several washes in 1× PBS, they were dehydrated through a methanol series and stored in 100% methanol at −20°C until use. After rehydration and several washes in 1× PBS/0.2% TritonX-100, specimens were blocked in 1× PBS/0.2%TritonX-100/2%BSA for 1 h at RT. Then they were incubated overnight at 4°C with rabbit anti-serotonin antibody (Sigma) at 1:500 dilution. The specimens were subsequently washed several times in 1× PBS/0.2% TritonX-100 and later incubated for 1 h with the secondary antibody FITC-labeled anti-rabbit immunoserum (Sigma; dilution 1: 200). After several final washes, specimens were mounted in Fluoromount media (SouthernBiotech) and examined with an inverted confocal SPII Leica microscope. Image analysis was carried out using the software package: Leica Confocal Software.
Transmission electronic microscopy
The hatchlings were first relaxed with a solution of 7.14% MgCl2 (made in ASW) for 5 min at RT. Then they were prefixed for 24 h at 4°C in a solution of 4% paraformaldehyde and 2.5% glutaraldehyde, made in a phosphate buffer 0.1 M pH 7.3. After several washes in phosphate buffer 0.1 M pH 7.3, they were post-fixed in 1% osmium tetraoxide (made in phosphate buffer 0.1 M pH 7.3) for 1 h at 4°C. Specimens were later washed several times in distilled water. Finally they were dehydrated through an acetone series at 4°C. These animals were embedded in Spurr resin. Transverse ultrathin sections of 60-70 nm thickness were produced in an Ultracut E ultramicrotome (Reichert-Jung) and collected on formvar-coated copper slot grids. The grids were stained with saturated uranyl acetate for 30 min at 37°C, followed by the incubation in Reynolds lead citrate for 3 min. The entire body of the hatchling was sectioned. Two to three ultrathin sections are cut every 1 µm along the first 40 μm of the animal’s body. From here to the posterior end of the animal, the ultrathin sections were cut every 2 µm. The sections were examined with a transmission electron microscope (JEOL 100CX operating at 80 kV). Pictures were taken on type 4489 EM film (Kodak). As pictures were taken at high magnification, every section is represented, on average, by 30 negatives. The negatives were subsequently digitalized using a scanner HP Scanjet 7400c with the software Epson Perfection 4990 Photo.
Two digital 3D models of the nervous system were produced: one from confocal stacks and the other from transmission electronic microscopy (TEM) serial sections. The first model was generated using the software TrakEM 2.0 (Albert Cardona; UCLA; with an Image J plug-in for three-dimensional modeling, see http://www.ini.uzh.ch/∼acardona/trakem2.html). The axonal processes, the sensory neurons, the nerve cords, and the central nervous system, which were revealed by the anti-tyrosin tubulin antibody, were outlined using the modeling functions. The traces were rendered in the program to generate a 3D model of the hatchling’s nervous system. A second model, based on serial transmission electron microscope sections of S. roscoffensis, was generated using the same software. First, the 30 negatives representing each given section were “stitched” electronically into a montage. Subsequently, montages of 73 sections were aligned and combined into a “stack”. Using the various modeling functions offered by TrakEM2, ciliary receptors, neuropile, and axon bundles were segmented, after which they could be displayed as a 3D digital model. Note that, given the relatively large gaps between adjacent sections, counts of individual cells (in particular sensory receptors) are not particularly accurate, given that the size of the ciliated apical pole of these cells is smaller than the average interval between sections. However, counts of all classes of receptors are affected by this shortcoming equally, so that our conclusions regarding (approximate) relative frequency of different sensory cells should be realistic.
The pattern of the brain neuropile and nerve cords
The brain neuropile comprises two bilateral, roughly triangular domains that flank the statocyst and are linked by three commissures (Fig. 2a, c, g). From anterior to posterior, we distinguish commissures c1, c2 and c3. C1 and c2 cross-anterior and posterior of the statocyst, respectively; c3 interconnects the posterior tips of the neuropile. The ventral longitudinal nerve cords enter the brain at the level of commissure c1 (Fig. 2b); the dlc at the level of c2; and the dmc at the level of c3 (Fig. 2a, c). Numerous thinner and shorter fiber bundles radiate out from the neuropile towards the epidermis at the anterior tip of the body (Fig. 2b).
The nerve cords extend posteriorly along the entire length of the body (Fig. 2a, c, g). Anteriorly, the cords are located deeper and appear thicker, possibly as a result of containing more fibers. Towards posteriorly, cords become thinner and come closer to the basal surface of the epidermis. Anteriorly at the level of the commissure c1, the ventral nerve cord is bifurcated, forming a short longitudinal branch that extends ventral of and parallel to the main cord until the level of commissure c3, where it ends blindly (Fig. 2b, g). In the trunk region, neighboring cords are interconnected by somewhat irregularly distributed anastomoses. In the specimen shown in Fig. 2a, b, four anastomoses connect the dorso-medial cords (commissures c4–c7); 4–5 anastomoses connect the dorso-medial with the dorso-lateral cords, and the dorso-lateral with the ventral cords (see inset of Fig. 2b). Neuronal cell bodies, preferentially clustered at the points of intersection of cords and anastomoses, flank the cords.
Anti-serotonin antibody reveals several neurons forming part of the brain and nerve cords. Labeling is found along the entire length of the ventral and both dorsal cords, the commissures surrounding the statocyst, and most transverse anastomoses of the trunk (Fig. 2e, f). Fibers and varicosities (presumably transmitter release sites; Falck 1962; Furness 1970) are strongly labeled, whereas neuronal cell bodies are difficult to discern. An exception are clustered cell bodies located in the epidermis at the anterior tip; these cells project (sensory) neurites towards the neuropile (Fig. 2f, inset).
Ultrastructure of the brain
Characteristic sizes and shapes of synaptic vesicles allow one to define different classes of presynaptic neurites (for nomenclature, see Bedini and Lanfranchi 1991).
Type 1 neurites are characterized by the presence of small clear vesicles (sv) of 20-40 nm in diameter (Fig. 5a). This is the most abundant neurite type found in the neuropile. Small clear vesicles are mostly restricted to terminal neurite branches and synapses; in some cases, they are also found in neuronal somata (Fig. 5b).
Type 2 neurites are characterized by the presence of dense-core vesicles (dcv; Fig. 5a–d) with a diameter of 60–120 nm. These vesicles contain granular material surrounded by a clear halo. We could identify numerous cell bodies (Fig. 5b), among them sensory cells integrated within the epidermis (Fig. 5d), which also contained dense-core vesicles. In some cases, both sv and dcv can occur within the same type of neuron (Fig. 5c).
Type 3 neurites have 60–90 nm granules with homogenously dense content (Fig. 5e, f). These granules have the typical characteristics described for the peptide containing vesicles of neurosecretory cells (Bedini and Lanfranchi 1991). Aside from neurites, we could identify numerous cell bodies of neurosecretory cells in the cortex (Fig. 5e).
Numerous neurons were observed to house large vesicular organelles (lv) of different diameters and texture; an example is shown in Fig. 5a. The function of these organelles, which have also been described in the literature (e.g., Bedini and Lanfranchi 1991) is not clear.
Aside from the profiles of typical cylindrical neurites, we observed irregularly shaped, highly electron-dense profiles that appear to correspond to lamellar, glia-like processes around groups of neurites (Fig. 5g, h). They occurred in the central neuropile and nerve cords. The cell bodies associated with these irregular profiles are electron-dense, often with hyper-dense nuclei filling almost the entire volume of the cell (Fig. 5h). Without additional markers it is difficult to clearly interpret this cell type. In several instances (e.g., Fig. 5h), cell bodies of these lamellated cells resembled apoptotic neuronal somata (see, for example, Fig. 3g in Larsen et al. 2009, illustrating apoptotic neurons in Drosophila larvae). More detailed studies and the use of markers for apoptosis will be required to get a clearer picture regarding the nature of the “glia-like cells” we describe here.
Although the method of sectioning did not allow reconstruct the three-dimensional architecture of terminal neurites in the neuropile, it is clear that many synapses are of the “en passant” type. Thus, terminal axonal branches form multiple swellings (“boutons” or “varicosities”) along their path which are filled with mitochondria and carry the presynaptic sites.
Ultrastructure of the nerve cords, peripheral nerve net and sensory neurons
Non-collared (type I) receptors with a hollow ciliary rootlet containing a granulated core (Fig. 9a, b) have a central cilium that is anchored by a wide, hollow, striated rootlet containing a granulated core (Fig. 9a: cilium not shown on the panel). The receptor apex lies above the level of the surrounding cells. The core of the rootlet contains granulated material and is always associated with a mitochondrion. Dense core vesicles are located in the basal cytoplasm. These receptors seem to be restricted to the head (Fig. 9b; violet).
Collared (type II) receptors with granular body
This type of receptor cell, which is by far the most common type (50%) is characterized by the presence of one long central single cilium surrounded by six microvilli. Instead of the rootlet, this receptor type contains a different kind of cytoplasmic specialization, called granular body, underneath the cilium (Fig. 9d). Of the six microvilli, two are located centrally adjacent to the cilium; the others are located more peripherally. The two central microvilli are extended by bundles of microfilaments which pass through the granular body (Fig. 9d, arrow). Collared receptors with granular bodies are regularly distributed along the nerve cords (Fig. 9b, in orange). In fact, each nerve cord, including the short and thin anterior branch of the ventral cord, is associated with one row (containing, in average, nine cells) of this type of receptor (Fig. 9b-d).
Collared receptors with rootlet (Fig. 9e)
This type of collared receptors accounts for 16% of all sensory cells. Its cilium is anchored by a single rootlet formed by an outer striated mantle and a core of granulated material. Proximally, the rootlet is split into numerous short, longitudinal, and oblique striated elements. These receptors are mainly formed ventrally and anteriorly (Fig. 9b, in blue).
Collared receptors with obliquely radial filament bundles in the cell apex (Fig. 9f)
The central cilium is flanked by two lateral microvilli from which prominent rootlets extend basally. The apical part of the receptor contains many dense-core vesicles. Unfortunately, our sections do not allow a more detailed description of the main rootlet in this ciliated receptor type. This type of sensory receptor is very rare. Only a few representatives of this sensory receptor were observed, mainly on the dorsal side (Fig. 9b, in red).
Structure of the acoel central nervous system
Hatchlings of S. roscoffensis possess an anterior brain, consisting of a cortex of neuronal cell bodies surrounding a central neuropile. The brain is generally similar to that described for C. (Symsagittifera) schultzii (Delage 1886) and also resembles the juvenile brain of the macrostomid M. lignano (Morris et al. 2007), although there are some notable differences. The macrostomid brain does not have a central statocyst. The neuropile forms a single crescent-shaped structure crossing the midline. Commissures form a dorsal and a ventral system of four to six bundles each, and are all embedded in the neuropile. In addition to these transverse systems of axons, vertical and longitudinally fiber bundles subdivide the macrostomid brain neuropile into several discrete compartments. A comparable compartmentalization is not evident in the considerably smaller neuropile of S. roscoffensis.
In more derived neoophoran platyhelminths the brain of adults is also larger and more complex than that of acoels. In the triclads Dugesia japonica and Schmidtea mediterranea (Agata et al. 1998; Cebrià et al. 2002; Cebrià 2008; Agata 2008) the brain consists of two lobes forming a large U-shaped structure from which nine pairs of branches project to the surface of the head region (Agata 2008).
The notion by Raikova (2004) that acoels do not have a “true” compact brain which contradicts the findings of this study and other papers (e.g., Reisinger 1925; Ramachandra et al. 2000; Tyler 2001; Achatz et al. 2010) can be explained in view of the different approach taken and different stages analyzed. Raikova (2004) used antibodies against serotonin, FMRFamide and GYIRFamide to label adult specimens of Nemertodermitida and Acoela. These markers label small subsets of neurons in the brain of most invertebrates, including various rhabditophoran flatworms (Raikova 2004; Morris et al. 2007; Cebrià 2008). For example, in acoels, as shown in the present study, the antibody against serotonin reveals one to two axons in each of the nerve cords and some of the commissures. Moreover, the location of cell bodies is all but invisible using antibodies against neurotransmitters, in particular, in case of mature nervous systems. The bulk of neuropile, surrounding the statocyst, and the surrounding cortex is not labeled by anti-serotonin or any other transmitter marker used in the literature. Finally, the relative size of the brain apparently diminishes with postembryonic development. Thus, the brain of acoel adult specimens studied by Raikova (2004) is very small compared to overall body size, and was dismissed as the “statocyst ganglion” (sensu Reisinger 1925). In its place, the superficial network of longitudinal nerve cords, connected by commissures, was considered as a “commissural brain”. However, we would postulate that the “statocyst ganglion”, which in the hatchling fills much of the anterior one third of the body and has the characteristic appearance of an invertebrate ganglion with a cortex of somata surrounding a central neuropile, represents the acoel brain.
Beyond the difference in calling the brain “statocyst ganglion”, the pattern of nerve cords and commissures and the distribution of serotonergic neurons described here for S. roscoffensis is similar to that seen by Raikova (2004) and Achatz et al. (2010) in other acoel species. Thus, in hatchlings of S. rosocoffensis, three pairs of longitudinal nerve cords run along the animal body: two dorsal and one ventral. Each pair originates anteriorly to the statocyst as a rosette of perikarya and consists of about 50 neurites. Several commissures linking the nerve cords are regularly distributed along the tracks. This pattern also corresponds closely to that of Convoluta niphoni (Achatz et al. 2010) and Isodiametra pulcra Achatz (2007). The nervous system of C. niphoni and S. roscoffensis share several structures: including the paired ventral nerve cords, the neuropile surrounding the statocyst, the ventral ring of the neuropile surrounded by a loose cellular cortex, the dorsal nerve cords that do not merge together in their anterior region, the transverse connections between the lateral (outer), and the medial (inner) dorsal nerve cords. A neuropile surrounding the statocyst is also present in I. pulchra that is not closely related to S. roscoffensis. The anterior commissural ring revealed by the 5-HT antibody has been detected in other members of the Acoela (Actinoposthiidae, Childiidae) and in Nemertodermatida (Nemertoderma westbladi and Flagellophora apelti), prompting Raikova (2004) to suggest that this ring is an ancestral character of the nervous system for the Acoela (or Acoelomorpha if we accept its monophyly; Hejnol et al. 2009). The three pairs of frontal branches containing serotonergic fibers are reminiscent of the so-called “anterior nerve fibers” described in N. westbladi (Nemertodermatida) and also of the so-called “sensory cells” present in Avagina incola (Acoela, Isodiametridae) and Childia groenlandica (Acoela, Childiidae) (Raikova 2004). Finally, the anterior clusters of serotonergic cell bodies, which are located on the lateral side of commissure c2 in S. roscoffensis, are similar to those revealed by the anti-GYIRF antibody in A. incola (Acoela, Isodiametridae).
Neurons, neurites, and synapses
Neuronal types can be classified using different criteria. Among others, the vesicular content has been used to distinguish neurons in many animal systems (Bedini and Lanfranchi 1991; Biserova et al. 2000; Reuter and Halton 2001). The three most common types of vesicles (sv, dcv, and lv) found in the nervous system of all phyla (e.g., Platyhelminths, Arthropoda, Vertebrata) are also found in S. roscoffensis. The presence of these vesicles in neurons is not mutually exclusive. Indeed in S. roscoffensis (Fig. 3d), as well as in Amphilinea foliacea (Platyhelminthes, Polycladida; Biserova et al. 2000), both sv and dcv can be distinguished in the same neuronal processes. However, in comparison to C. (S) psammophila, a well-described species, the hatchling S. roscoffensis is missing one neuronal type, the third neuronal type of C. (S.) psammophila, which is characterized by large vesicles (Bedini and Lanfranchi 1991). We cannot rule out the possibility that this type will develop later during the development or alternatively that it has been lost during evolution of the genus Symsagittifera.
The existence of glia-like cells with lamelliform, electron-dense processes is unusual for flatworms (Bedini and Lanfranchi 1991). Cells with some attributes of glia were reported in several ultrastructural studies of parasitic flatworms (Biserova et al. 2000) and of a few acoel species (Bedini and Lanfranchi 1991), where the glia-like cells are characterized by a spherical nucleus surrounded by a narrow cytoplasmic sheet provided with very few organelles, and some of its attenuated cytoplasmic projections extend into the surrounding nervous tissue. In contrast, in vertebrates and “higher” invertebrates (e.g., arthropods, annelids, molluscs), glial sheaths form envelopes around peripheral nerves, central axon bundles, or neuronal somata. The glia-like cells shown here in S. roscoffensis, when considering morphology, come closest to “true” glial cells as they exist in “higher phyla”. Even though the glia-like cells do not form complete sheaths around the central neuropile or nerve cords, their lamelliform processes are extensive and they may well isolate some of the bundles of axons from each other or from other elements of the neuropile/nerve cords.
Asymmetric and symmetric synapses in the hatchlings of S. roscoffensis establish contact between the different neurons forming the central nervous system, nerve cords, and the peripheral nervous plexus. In the classical electron microscopy literature, asymmetric synapses are typically excitatory and associated with small clear synaptic vesicles. Symmetric synapses contain pleomorphic vesicles of more irregular shape and different sizes and have been linked to inhibitory transmission. However, combined physiological and structural work is required to arrive at firm conclusions in regard to correlations between function and morphology of synapses in the acoel nervous system.
A specific asymmetric synapse, the ribbon type, is observed in the central nervous system. This synaptic element is characteristic of “more advanced” invertebrate phyla (e.g., arthropods), where it appears to function as a specialized organelle involved in docking of synaptic vesicles (Schmitz 2009). Synaptic ribbons have been previously reported for otoplanid (Bedini and Lanfranchi 1991), suggesting the ancient origin of this structure.
Cells with structural characteristics of neoblasts
Neoblasts represent a unique system of totipotent stem cells that exist throughout the lifetime of adult flatworms, both Rhabditophora and Acoela. Neoblasts are able to associate with all organs and differentiate into the corresponding cell types. In Acoela, the presence of neoblasts has already been shown in Convolutriloba longifissura (Gschwentner et al. 2001) and Isodiametra pulchra (De Mulder et al. 2009). Neoblasts have a high nucleocytoplasmic ratio, few mitochondria and free ribosomes, and the nucleus consists of uncondensed chromatin with few smaller clumps of condensed chromatin. The neoblasts are located in the peripheral parenchyma. Cells with these properties are common in our electron microscopic material. As in I. pulchra, the neoblast-like cells of S. roscoffensis are located along the lateral side of the animal; fewer cells were present closer to the midline and almost absent anterior to the statocyst. Unlike I. pulchra, in S. roscoffensis, a cluster of neoblast-like cells are clustered posterior to the brain. Neoblasts are crucial for tissue homeostasis, development, and regeneration (De Mulder et al. 2009), as well as fission, as shown in C. longifissura (Acoela, Sagittiferidae; Gaerber et al. 2007). After fission (asexual reproduction), the nervous system in C. longifissura is reorganized and develops new neurons lying alongside the in-growing nerve cords, from which axons start to grow posteriorly. S. roscoffensis does not reproduce by fission. Besides S. roscoffensis is not able to regenerate a new head, as I. pulchra (De Mulder et al. 2009). However, after posterior amputation of the body, the animals are able to regenerate the lost body part and recover their initial size (A. Bery, unpublished data). The classical experiments of Hanson (1967) and the more recent work of Url (2009 bachelor’s thesis) and De Mulder et al. (2009) reported a similar regeneration capacity in several members of the acoel family, Convolutidae. Thus, the presence of neoblast-like cells along the nerve cord may represent a common feature in acoels, at least in the three families Convolutidae, Isodiametridae and Sagittiferidae (including C. longifissura, I. pulchra, and S. roscoffensis).
The nerve net and sensory neurons
The nerve net in hatchlings of S. roscoffensis contains numerous subepidermal elements at the periphery of the musculature, as well as deep fibers associated with the musculature. It resembles the pattern described for all Acoela and Nemertodermatida (Raikova 2004), as well as rhabditophoran flatworms (Kotikova and Raikova 2008). At least four different types of sensory cells were distinguished in juvenile S. roscoffensis. Their concentration in the anterior part of the body suggests that the sensory receptors could play a role in the specific “searching/tasting/sniffing” behavior that is characteristic for this animal. The sensory receptors contain dense vesicles of the neurosecretory type, suggesting that sensory cells produce and release peptides. Similar vesicles have been reported in S. psammophila (Bedini et al. 1973), where vesicles are concentrated in sites of contact between the basal membrane of the receptor cells and neurites of the subepidermal plexus.
Non-collared receptors with a hollow ciliary rootlet containing a granulated core (type I in Bedini et al. 1973; type 3 in Todt and Tyler 2007) are common in the genus Symsagittifera. They are similar to the Ct1 receptor described in Convoluta thela. In both Symsagittifera and Convoluta these receptors often occur in clusters of four to eight cells. The same has been reported for various species of the rhabditophoran clade Macrostomida, where non-collared receptors occur in groups and are typically associated with glandular cells, whereas collared receptors are singlets and are not directly adjacent to glands (Xylander et al. 1997).
The collared receptors without rootlet (type II in Bedini et al. 1973; type 5 in Todt and Tyler 2007) have been described in I. pulchra (Acoela, Isodiametridae) (Pfistermüller and Tyler 2002), Proporus bermudensis (Acoela, Proporidae; P3 receptor), Convoluta convoluta (Acoela, Convolutidae; Cc3 receptor), and C. thela (Acoela, Convolutidae) (Ct3 receptor; Todt and Tyler 2007). In these species, the microvilli of the collar, which encircle the sensory cilium, are thick, straight, and heavily reinforced with microfilaments. A granular body replaces the striated rootlet. Although the general morphology of these receptors is similar, a few differences can be detected between species, mainly in the number of peripheral microvilli forming the collar, and the connection of central microvilli to the granular body (Pfistermüller and Tyler 2002). Outside the Acoela, collared receptors with granular bodies (also called tubular bodies) have been reported for rhabditophorans (e.g., Microstomum; Rieger et al. 1991), cnidarians (Holtmann and Thurm 2001) and ctenophores (Tamm and Tamm 1991). In the latter phylum, these receptors are termed actin pegs cilia and they are assumed to have chemosensory and/or mechanosensory functions.
The collared receptors with obliquely radial filament bundles in the cell apex (type 4 in Todt and Tyler 2007) are very common among Acoela; they were reported in nine of the 13 families studied by Todt and Tyler (2007), including C. convoluta and C. thela. In the latter species, these collared receptors bear obliquely radial filament bundles in the cell apex and a single hollow ciliary rootlet, which is composed of numerous strand-like elements. Unfortunately, our sections do not allow for a fine description of the main rootlet of this ciliated receptor type.
Our data indicate that the juvenile acoel central nervous system, at the light and ultrastructural level, shows all the hallmarks of an invertebrate ganglion, similar to what has been described for Rhabditophora and juvenile forms of other invertebrate taxa. In other words, our data do not support the assertion made in several previous papers that Acoela differ from rhabditophoran flatworms in terms of qualitative features of their central nervous system. Thus, hatchlings of S. roscoffensis possess a brain that is structured like a typical invertebrate ganglion, similar to what has been described for Rhabditophora and juvenile forms of other invertebrate taxa. It is of course well possible that the shape and connectivity of individual neurons in acoles show characteristic features that would set them apart from other flatworms; the availability of specific markers in the near future will help to settle this issue.
AB received an EC fellowship within the MOLMORPH network under the 6th Framework Programme “Marie Curie Host Fellowships for Early Stage Research Training (EST) (contract number MEST-CT-2005 – 020542).” We thank M. Ciluffo (UCLA) for sectioning and preparing the blocks for electron microscopy. The acquisition of images was carried out with the help of M. Ciluffo, M. de Miguel-Bonet, and scientific personnel at the Confocal microscopy facility, UB Finally, we thank A. Wanninger, O. Raikova, and P. Ladurner, and their departmental colleagues, for commenting on the study and sharing their knowledge of acoel morphology.
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