Ultrastructure of the tentacle nerve plexus and putative neural pathways in sea anemones

Abstract. Neurons of sea anemone tentacles receive stimuli via sensory cells and process and transmit information via a plexus of nerve fibers. The nerve plexus is best revealed by scanning electron microscopy of epidermal peels of the tentacles. The nerve plexus lies above the epidermal muscular layer where it appears as numerous parallel longitudinal and short interconnected nerve fibers in Calliactis parasitica . Bipolar and multipolar neurons are present and neurites form interneuronal and neuromuscular synaptic contacts. Transmission electron microscopy of cross sections of tentacles of small animals, both C. parasitica and Aiptasia pallida , reveals bundles of 50–100 nerve fibers lying above groups of longitudinal muscle fibers separated by intrusions of mesoglea. Smaller groups of 10–50 slender nerve fibers are oriented at right angles to the circular muscle formed by the bases of the digestive cells. The unmyelinated nerve fibers lack any glial wrapping, although some bundles of epidermal fibers are partially enveloped by cytoplasmic extensions of the muscle cells; small gastrodermal nerve bundles lie between digestive epithelial cells above their basal myonemes. A hypothetical model for sensory input and motor output in the epidermal and gastrodermal nerve plexuses of sea anemones is proposed.     

Antisera to the sequence Arg-Phe-amide visualize neuronal centralization in hydroid polyps

Summary Antisera to the sequence Arg-Phe-amide (RF-amide) have a high affinity to the nervous system of fixed hydroid polyps. Whole-mount incubations of several Hydra species with RFamide antisera visualize the three-dimensional structure of an ectodermal nervous system in the hypostome, tentacles, gastric region and peduncle. In the hypostome of Hydra attenuata a ganglion-like structure occurs, consisting of numerous sensory cells located in a region around the mouth opening and a dense plexus of processes which project mostly radially towards the bases of the tentacles. In Hydra oligactis an ectodermal nerve ring was observed lying at the border of hypostome and tentacle bases. This nerve ring consists of a few large ganglion cells with thick processes forming a circle around the hypostome. This is the first direct demonstration of a nerve ring in a hydroid polyp.Incubation of Hydractinia echinata gastrozooids with RFamide antisera visualizes an extremly dense plexus of neuronal processes in body and head regions. A ring of sensory cells around the mouth opening is the first group of neurons to show RFamide immunoreactivity during the development of a primary polyp. In gonozooids the oocytes and spermatophores are covered with strongly immunoreactive neurons.All examples of whole-mount incubations with RF-amide antisera clearly show that hydroid polyps have by no means a diffuse nerve net, as is often believed, and that neuronal centralization and plexus formation are common in these animals. The examples also show that treatment of intact fixed animals with RFamide antisera is a useful technique to study the anatomy or development of a principal portion of the hydroid nervous system.     

Fine structural studies of the nervous system and the apical organ in the planula larva of the sea anemone Anthopleura elegantissima

The nervous system of the planula larva of Anthopleura elegantissima consists of an apical organ, one type of endodermal receptor cell, two types of ectodermal receptor cells, central neurons and nerve plexus. Both interneural and neuromuscular synapses are found in the nerve plexus. The apical organ is a collection of about 100 long, columnar cells each bearing a long cilium and a collar of about 10 microvilli. The cilia of the apical organ are twisted together to form an apical tuft. The ciliary rootlets of the apical organ cells are extremely long, reaching to the basal processes of the cells adjacent to the mesoglea. All three types of sensory cells are tall and slender in profile and are identified by the presence of one or more of the following features: microtubules, small vesicles, membrane-bound granules and synapses. The interneurons are bipolar cells with somas restricted to the aboral end, adjacent to the apical organ. All synapses observed are polarized or asymmetrical. A diagram including all the elements of the nervous system is presented and the possible functions of the nervous system are discussed in relation to larval behavior.     

New insights on ctenophore neural anatomy: immunofluorescence study in Pleurobrachia pileus (Müller, 1776)

Ctenophores are non-bilaterian animals sharing with cnidarians and bilaterians the presence of sensory receptors, nerve cells, and synapses, absent in placozoans and sponges. Although recent immunofluorescence studies have renewed our knowledge of cnidarian neuro-anatomy, ctenophores have been much less investigated despite their importance to understanding the origin and early evolution of the nervous system. In this study, the neuro-anatomy of the ctenophore Pleurobrachia pileus (Müller, 1776) was explored by whole-mount fluorescent antibody staining using antibodies against tyrosylated -tubulin, FMRFamide, and vasopressin. We describe the morphology of nerve nets and their local specializations, and the organization of the aboral neuro-sensory complex comprising the apical organ and polar fields. Two distinct nerve nets are distinguished: a mesogleal nerve net, loosely organized throughout body mesoglea, and a much more compact “nerve net” with polygonal meshes in the ectodermal epithelium. The latter is organized as a plexus of short nerve cords. This epithelial nervous system contains distinct sub-populations of dispersed FMRFamide and vasopressin immunoreactive nerve cells. In the aboral neuro-sensory complex, our most significant observations include specialized nerve nets underlying the apical organ and polar fields, a tangential bundle of actin-rich fibers (interpreted as a muscle) within the polar fields, and distinct groups of neurons labeled by anti-FMRFamide and anti-vasopressin antibodies, within the apical organ floor. These results are discussed in a comparative perspective.     

Le système nerveux des cténaires

Summary Ultrastructural evidence is given of the occurrence of nervous elements in the mesoglea of Ctenophores based on the presence of the typical synapses of this phylum.In Beroids, nervous fibers from the ectodermal nerve-net cross the epithelial basal membrane and run through the mesoglea; they are devoid of any ensheathing cell. These neurites build highly differentiated synapses upon the muscles and upon peculiar cells, tentatively named mesenchymal cells.In Cydippids, nerve fibers and nerve cell-bodies have been observed in the mesoglea of the tentacles. The mesogleal core of each tentacle contains mesenchymal cells and a thick strand of neurons and neurites, forming a kind of elongated ganglion. Neurites of either the axial neurones or the epithelial nerve-net neurones form numerous radial nerve strands across the tentacular muscles. Interneural, neuro-muscular and neuro-mesenchymal junctions are very frequent in the tentacle.As far as the organization of the mesoglea is concerned, the Ctenophora thus appear closer to Turbellaria than to Cnidaria.

Ce travail a bénéficié de la collaboration technique de Madame J. Amsellem que nous remercions vivement.     

The nervous system of parasitic cnidarian Polypodium hydriforme

The nervous system of intracellular parasitic cnidarian Polypodium hydriforme at various stages of its life cycle has been studied by the immunocytochemical method using antibodies to FMRF-amide and by electron microscopy. Neurosecretory, sensory, and ganglion cells have been identified both at the parasitic stage (planula and stolon stages, when body layers are inverted) and in free-living animals. These cells are characterized by the presence of round neurosecretory granules about 80–120 nm in diameter. Gap junctions have been detected between nerve cells. Most of the neurosecretory and sensory cells have been observed in the epidermis of sensory tentacles of free-living animals. Sensory cells possess immobile flagella. The chains of ganglion cells are located under the epidermis and penetrate mesoglea. A centriole encircled by a fragment of nuclear envelope, which is a marker of ectodermal lineage cells in Polypodium, has been described in the cytoplasm of the sensory cells, thus proving the ectodermal nature of the nervous system. Like in most cnidarians, the nervous system of Polypodium hydriforme is a network containing FMRF-amide-like neuropeptides. Neither sense organs, nor ring-shaped nerve concentrations have been observed.     

Primary sensory neurons containing command neuron peptide constitute a morphologically distinct class of sensory neurons in the terrestrial snail

In the central nervous system of the terrestrial snail Helix, the gene HCS2, which encodes several neuropeptides of the CNP (command neuron peptide) family, is mostly expressed in cells related to withdrawal behavior. In the present work, we demonstrate that a small percentage (0.1%) of the sensory cells, located in the sensory pad and in the surrounding epithelial region ("collar") of the anterior and posterior tentacles, is immunoreactive to antisera raised against the neuropeptides CNP2 and CNP4, encoded by the HCS2 gene. No CNP-like-immunoreactive neurons have been detected among the tentacular ganglionic interneurons. The CNP-like-immunoreactive fiber bundles enter the cerebral ganglia within the nerves of the tentacles (tentacular nerve and medial lip nerve) and innervate the metacerebral lobe, viz., the integrative brain region well-known as the target area for many cerebral ganglia nerves. The procerebral lobe, which is involved in the processing of olfactory information, is not CNP-immunoreactive. Our data suggest that the sensory cells, which contain the CNP neuropeptides, belong to a class of sensory neurons with a specific function, presumably involved in the withdrawal behavior of the snail.     

Cytologische Veränderungen während der Metamorphose des CubopolypenTripedalia cystophora (Cubozoa,Carybdeidae) in die Meduse

The life cycle ofTripedalia cystophora includes a sessile saclike polyp — the asexual reproducing form — and a pelagic tetraradial medusa — the sexually reproducing generation. Medusan development can be induced by temperature increase. It reveals neither budding nor strobilation, but a real metamorphosis of a polyp to only one medusa. According to morphological and anatomical criteria the metamorphosis can be subdivided into four different stages: (1) four longitudinal furrows segment the polyp, the tentacles of which are apportionated on the four quadrants of the body. (2) The subumbrellar cavity develops by invagination of the peristom; the relicts of the fused tentacles change to four rhopalia buds. (3) Medusan architecture including four new interradial tentacles, four rhopalia and the subumbrellar swimming musculature is completed. (4) A young tetraradial medusa starts swimming. Ultrastructural analysis of those metamorphic stages show the different processes of morphogenesis: (a) Gastrodermal cells — absorptive and spumous cells — undergo transdifferentiation and proliferation to medusan cells of the same structure and function. (b) Epidermal cells, excluding the epithel muscle cells, dissociate and are autolytically withdrawn. Dedifferentiated epithel muscle cells — interstitial cells — regain the ability to develop a complete new set of somatic cells, not originally present in the polyp. They include amongst others cross-striated muscle cells, medusan typic nematocyts and particularly sensory and nervous cells. Those cells establish a nervous system with lens-eyes, simple ocelli, statocysts, diffuse nerve net and an additional nerve ring.     

The fine structure of the buccal tentacles of Holothuria forskali (Echinodermata,Holothuroidea)

Summary Ultrastructural study of the buccal tentacles of Holothuria forskali revealed that each tentacle bears numerous apical papillae. Each papilla consists of several differentiated sensory buds.The epidermis of the buds is composed of three cell types, i.e. mucus cells, ciliated cells, and glandular vesicular cells (GV cells). The GV cells have apical microvilli; they contain bundles of cross striated fibrillae associated with microtubules. Ciliated cells have a short non-motile cilium. Bud epidermal cells intimately contact an epineural nervous plate which is located slightly above the basement membrane of the epidermis. The epineural plate of each bud connects with the hyponeural nerve plexus of the tentacle. This nerve plexus consists of an axonic meshwork surrounded in places by sheath cells. The buccal tentacles have well-developed mesothelial muscles. Direct innervation of these muscles by the hyponeural nerve plexus was not seen.It is suggested that the buccal tentacles of H. forskali are sensory organs. They would recognize the organically richest areas of the sediment surface through the chemosensitive abilities of their apical buds. Tentacles presumably trap particles by wedging them between their buds and papillae.     

Neural system reorganization during metamorphosis in the planula larva of Clava multicornis (Hydrozoa, Cnidaria)

The planula larva of the hydroid Clava multicornis (Forskål, 1775) has a complex nervous system, characterized by the presence of distinct, anteriorly concentrated peptidergic populations of amidated neurons, presumably involved in the detection of environmental stimuli and metamorphic signals. Differently from other hydrozoan larvae in C. multicornis planulae GLW-positive cells with putative sensory role have a peculiar dome-shaped forefront organization, followed by a belt of RF-positive nerve cells. By immunohistochemistry, we investigated the transformation of the peptidergic (GLW-amide and RF-amide) larval neuroanatomy at different stages of metamorphosis and the subsequent development of the primary polyp nervous system. By terminal transferase-mediated dUTP nick end-labeling assay, apoptotic nuclei were first identified in the anterior pole of the settled larva, in the same region occupied by GLW-amide positive putative sensory cells. In primary polyps, GLW-amide positive signals first encircled the hypostome area, later extending downwards along the polyp column or upwards over the hypostome dome, whereas RF-amide positive sensory cells initially appeared at the tentacles base to later extend in the tentacles and the polyp column. In spite of the possession of distinct neuroanatomies, different cnidarian planulae may share common developmental mechanisms underlying metamorphosis, including apoptosis and de novo differentiation. Our data confirm the hypothesis that the developmental dynamics of tissue rearrangements may be not uniform across different taxa.     

Distribution of catecholamine-containing,serotonin-like and neuropeptide FMRFamide-like immunoreactive neurons and processes in the nervous system of the actinotroch larva ofPhoronis muelleri (Phoronida)

Summary Glyoxylic-acid-induced fluorescence of catecholamines and antibodies against serotonin and FMRFamide were used to study the distribution of putative neurotransmitters in the actinotroch larva ofPhoronis muelleri Selys-Longchamps, 1903. Catecholamines occur in the neuropile of the apical ganglion, in the longitudinal median epistome nerves, in the epistome marginal nerves, and in the nerve along the bases of the tentacles. The tentacles have laterofrontal and latero-abfrontal bundles of processes that form two minor nerves along the lateral ciliary band of the tentacles, and a medio-frontal bundle of processes. Monopolar cells are located on the ventro-lateral part of the mesosome. Processes are located along the posterior ciliary band and as a reticulum in the epidermis. Serotonin-like immunoreactive cells and processes are located in the apical ganglion, in the longitudinal median epistome nerves, and as a dorsal and ventral pair of bundles along the tentacle bases. Processes from the latter extend into the tentacles as the medioabfrontal processes. The latero-abfrontal processes form a minor nerve along the ciliary band. The dorsal bundles forms the major nerve ring along the tentacles and processes extend from it to the metasome. Processes are located along the posterior ciliary band. FMRFamide-like immunoreactive cells and processes are found in the apical ganglion, in the longitudinal median epistome nerves and as a pair of lateral epistome processes projecting towards the ring of tentacles. In the tentacles, a pair of latero-frontal processes are found; these form a minor nerve along the ciliary band. A band of cells can be seen along the tentacle ring.     

Scanning electron microscopy of the muscle system of Hydra magnipapillata

The fine structure of the ectodermal and endodermal muscle layers of Hydra magnipapillata has been analyzed by scanning electron microscopy after hydrolytic removal of the mesoglea with NaOH and subsequent exposure of the basal and lateral aspects of the layers by mechanical dissection. The ectodermal muscle layer consists of fibrous processes of epithelial cells extending longitudinally to the body axis, whereas the endodermal muscle layer comprises cells with hexagonal bases and several strands of myonemes oriented circularly. In each layer, the muscular elements tightly interdigitate, extending a continuous muscle sheet along the mesoglea. The ectodermal and endodermal muscle sheets communicate with each other via foliate microprojections penetrating the mesoglea. On the lateral aspect of the ectodermal epithelium, spiny nerve fibers run along the upper surface of the muscle processes. The spines are often attached to muscle processes, suggesting that the former monitor muscle contraction. Nerve fibers occasionally come into contact with the mesoglea through narrow gaps between the muscle processes. In the hypostomal ectoderm, a small spindle-shaped cell, probably sensory in nature, extends an apical cilium and a long basal process.     

Ultrastructure of the adhesive tentacles of the limnomedusa Vallentinia gabriella (Hydrozoa,Olindiadidae)

Summary The specialized adhesive exumbrellar tentacles of the limnomedusa Vallentinia gabriella were examined by light microscopy and scanning and transmission electron microscopy. The adhesive region first differentiates some distance from the tentacle tip. As differentiation proceeds the distal part is reduced and the adhesive region comes to lie at the tentacle tip. The adhesive epithelium consists of flagellated and non-flagellated glandular cells, a few nematocytes, and a nerve plexus. The glandular cells are characterized by electron-dense granules and bundles of microtubules. The microtubules, being anchored to the mesoglea, are oriented parallel to the longitudinal axis of the cell and extend up to the cell apex. It can be assumed that the microtubules are involved in the transport of secretory granules to the cell apex. Bundles of neurites run adjacent to the mesoglea between the basal processes of the glandular cells. The neurites form interneural synapses and synapses with glandular cells. It is suggested that detachment of the specialized adhesive tentacles is under nervous control.     

Light and electron microscopic localization of a monoclonal antibody in neurons in situ in the head region of Hydra

A mouse monoclonal antibody to Hydra attenuata was used to demonstrate immunoreactive product in neurons in situ, in both whole mount and sectioned hypostomes and tentacles of H. oligactis and H. littoralis. Immunoreactive cells were concentrated around the mouth and scattered along the length of the tentacles. In the hypostome, nerve cells sent one or more processes orally and the others aborally but the processes were more distinctly stained in H. oligactis. A thin strand of five to six perihypostomal neurons was present close to the hypostome-tentacle junction. In the tentacles, neurons with long processes contacted up to five different batteries of nematocysts. Neural processes were associated with nematocyst batteries in three ways: 1) forming a perikaryal loop to encircle a centrally located stenotele, 2) branching at a distance from the perikaryon to contact a variety of nematocysts, and 3) terminal branching by one or more neurons with contacts on one to several nematocysts within a battery. Immunocytochemical localization of neurons in Hydra by light microscopy was correlated for the first time with electron microscopy. Peroxidase-antiperoxidase (PAP)-positive sensory cells were concentrated around the mouth opening. PAP-positive ganglion cells were predominant in the tentacles. Sensory cells were elongate or spindle-shaped (unipolar), triangular with two oppositely directed processes (bipolar), and multipolar (tripolar or tetrapolar) with one of the processes extending to the epidermal surface. Ganglion cells were either unipolar or bipolar or multipolar, with neurites paralleling the mesoglea and occasionally having processes abut on it.     

Cytoskeletal elements in migrating and tentacle-integrated nematocytes of a marine hydrozoan

Summary— Actively migrating nematocytes of the marine polyp Stauridiosarsia producta are converted into completely immotile cells as soon as they become integrated in the ectodermal tissue of the tentacles. Immunocytochemical and electron microscopical methods revealed that cytoskeletal elements composed of actin, tubulin, centrin and a still unidentified protein are interwoven within the complete cell. While the organization of the sensory pole of the nematocyte, containing the cnidocil complex, the pseudovillar system and the distal half of a microtubular basket surrounding the nematocyst, is not affected by the transition from a motile to an immotile cell, the cytoskeletal elements in the basal portion of the cell are re-organized. Thus, the basolateral cytoplasm of migrating cells contains less organized microtubular arrays and bundles of about 10 nm-thick filaments. In the tentacle-integrated state, the 10-nm filaments are concentrated within a stalk-like foot which is stabilized by some rigid microtubular arrays derived from the microtubular basket. By elongation of the microtubular basket towards the cellular basis, the nematocyst becomes indirectly anchored at the mesoglea. As indicated by pharmacological treatments, the stiffness of the stalk depends on its microtubular content only.     

Evidence for a common pattern of peptidergic innervation of cnidocytes

Tentacles from representatives of all four classes of the phylum Cnidaria were examined using antibodies against the neuropeptides FMRFamide and RFamide to reveal the organization of neurons and nerve nets associated with cnidocytes. The tentacles of all species examined contained FMRFamide- or RFamide-immunoreactive neurons, in varying densities. In representatives from the Scyphozoa, Hydrozoa, and Cubozoa, the FMRFamide-immunoreactive neurons formed plexuses at the base of the cnidocyte assemblages; in anthozoans, the absence of discrete assemblies of cnidocytes precluded visual co-localization of cnidocytes and immunoreactive neurons. In all four classes, immunoreactive sensory cells connected these peptidergic nerve nets to the surface of the tentacle. These findings suggest that members of all four cnidarian classes share a common organizational pattern, and it is proposed that this peptidergic innervation may be involved in the chemosensory regulation of cnidocyte discharge.     

An ultrastructural study of larval settlement in the sea anemone Urticina crassicornis (Cnidaria,Actiniaria)

Laboratory-reared larvae of the sea anemone Urticina (= Tealia) crassicornis have been examined by electron microscopy prior to and following settlement on algal substrata. At 18 days postfertilization, the free-swimming planula larva measures about 600 μm long. A stomodaeal invagination occurs at the narrow end of the larva and connects with a solid mass of endoderm in the core region. The endoderm possesses septa with well-developed myonemes and is situated subjacent to a thin sheet of mesoglea. The uniformly ciliated ectoderm that constitutes the outer layer of the larva contains: (1) spirocysts, (2) nematocysts, (3) mucus, (4) three types of membrane-bound granules, (5) a basiepithelial nerve plexus, and (6) a few nongranular cells that may represent sensory neurons. Within several minutes after the introduction of the algal substratum, the planula characteristically directs its broadened aboral end toward the alga and secretes a refractile sheet of material. As the aboral end attaches to the substratum, the larva becomes noticeably shorter along its oral-aboral axis, presumably owing to the contractions of myonemes that are located within the endodermal septa. All three types of granules and the ectodermal mucoid substances are exocytosed during settlement, but spirocysts and nematocysts characteristically remain undischarged. Ovoid, PAS⁺ granules are believed to be at least partly responsible for adhesion, since these granules are concentrated at the aboral end prior to settlement and are somewhat similar in ultrastructure to putative viscid granules produced by other species. Contrary to a previous report based on light microscopy, no discrete sensory organ is evident in serial sections of the aboral ectoderm. The ability of planulae to detect suitable substrata appears to depend instead on sparsely distributed sensory cells that occur throughout the larval ectoderm.     

NADPH-diaphorase localization in the radial nerve cords of the starfish Patiria pectinifera

The presence and localization of NADPH-diaphorase (NADPH-d) in the radial nerve cords of Patiria pectonifera was shown by electron histochemistry. NADPH-d-positive structures were found in ectoneural and hyponeural regions of the radial nerve cord. Ultrastructural localization of NADPH-d was detected in neurons, sensory cells, supporting cells, and in the nerve plexus. The highest enzymatic activity in ectoneural region of the radial nerve cord is due, presumably, to the involvement of NADPH in sensory signal processing.     

The oral nerve plexus in amphioxus larvae: function,cell types and phylogenetic significance

Serial electron microscope reconstructions were used to examine the organization and cell types of the nerve plexus that surrounds the mouth in amphioxus larvae. The plexus is involved in a rejection response that occurs during feeding: a number of oral spines project across the mouth, and debris impinging on them triggers a contraction of the gill slit and pharyngeal musculature that forces water through the mouth, dislodging the debris. The oral spine cells are secondary sense cells that synapse with neurites belonging to a class of peripheral interneurons intrinsic to the oral nerve plexus. These in turn synapse with a second class of peripheral neurons with large axons that we interpret as sensory cells and which probably transmit signals to the nerve cord. The intrinsic cells also appear to synapse with each other, implying that local integrative activities of some complexity occur in the oral plexus. In comparative terms, the intrinsic neurons most closely resemble the Merkel-like accessory cells of vertebrate taste buds, and we postulate a homology between oral spine cells and taste buds, despite differences in function. There are also similarities between the amphioxus oral plexus and adoral nerves and ganglia of echinoderm larvae, suggesting homology of both the oral nerve plexus and the mouth itself between lower deuterostome phyla and chordates.