First evidence of unpigmented rhabdomeric photoreceptors in a Microstomum species (Plathelminthes, Macrostomorpha, Microstomidae) and ultrastructure of photoreceptor-like ciliary aggregations

Microstomum spiculifer possesses a pair of intracerebral photoreceptors each consisting of a single rhabdomeric sensory cell and two cup or mantle cells. The mantle cells are devoid of pigment. In addition, four so-called ciliary aggregations, presumed to have a light-sensing function, are present. Each ciliary aggregation represents a specialized cell with an internal cavity filled with axonemes of modified cilia. Rhabdomeric photoreceptors consisting of one to three sensory cells and a single pigmented or unpigmented mantle cell are widespread within taxa of the Plathelminthes Rhabditophora. On the contrary, the existence of two mantle cells forming the eye cup is only known for M. spiculifer and a few other species of the Macrostomida. Therefore, at least two hypotheses are possible: (1) two cup cells are a basic characteristic of the Rhabditophora and a reduction from two to one cup cell has occurred secondarily or (2) the stem species of the Rhabditophora possessed rhabdomeric eyes with one cup cell, and two mantle cells have evolved within the Macrostomorpha. The existence of ciliary aggregates has been documented for several taxa of the Plathelminthes Rhabditophora. From their distribution it can not be concluded whether these differentiations are either a basic feature of the Rhabditophora or have evolved several times convergently. Accepted: 26 September 1999     

Ultrastructure of free neuromasts of Bathygobius fuscus (gobiidae) and canal neuromasts of Apogon cyanosoma (apogonidae)

Light and electron microscopic observations were made on the lateral line organs of the free neuromasts of the goby Bathygobius fuscus and the canal neuromasts of the cardinal fish Apogon cyanosoma. As in other lateral line systems, each neuromast consists of hair cells, supporting cells and mantle supporting cells, the whole being covered by a cupula. In B. fuscus the free neuromasts are mounted on papillae and have hair cells with stereocilia up to 2.5 μm long and a single kinocilium at least 25 μm long. Each neuromast is covered by a vane-like cupula that can be divided into two regions. The central region over the sensory area contains columns of myelin-like figures. These figures are absent from the outer region covering the mantle. The canal neuromasts of A. cyanosoma are diamond-shaped with up to 1,500 hair cells. The cupula is unusual in having a channel that lies over the sensory region. The hair cells have up to 45 stereocilia, the tallest reaching 2.5 μm, and a kinocilium at least 5 μm long. Tip links are shown for the first time between rows of stereocilia of the hair cells of lateral line neuromasts. The presence of tip links has now been demonstrated for all acousticolateral hair cell systems.     

The fine structure of the lateral-line organs of larval Ichthyophis (Amphibia: Gymnophiona)

Light and electron microscopic observations of the lateral-line organs of larval Ichthyophis kohtaoensis confirmed earlier reports of the occurrence of two different types of lateral-line organs. One type, the ampullary organ, possesses 15–26 egg-shaped sensory cells. Each sensory cell extends a single kinocilium surrounded by a few microvilli into the ampullary lumen. This is in contrast to the ampullary organs of urodele amphibians that contain only microvilli. The second type of organ, the ordinary neuromast, has 15–24 pear-shaped sensory cells arranged in two to three rows. Each sensory cell shows a kinocilium that is asymmetrically placed with respect to both a basal plate and approximately 60 stereovilli. The sensory cells of ampullary organs are always separated by supporting cells; those of neuromasts are occasionally in contact with one another. Numerous (neuromasts) or few (ampullary organs) mantle cells separate the organs from the epidermal cells. Only afferent synapses are found in the ampullary organs whereas vesicle-filled fibers together with afferent nerve terminals are found in neuromasts. Both organs contain similarly sized presynaptic spheres adjacent to the afferent fibers. It is suggested that the neuromasts have a mechanoreceptive function, whereas the ampullary organs have an electroreceptive one.     

Ultrastructural study of metamorphosis in the freshwater bryozoan Plumatella fungosa (Bryozoa,Phylactolaemata)

Summary

At metamorphosis the attachment of the Plumatella larva to the substrate is effected by secretions from glandular cells in the apical plate, the leading pole during swimming. The larval mantle folds back and slides down towards the substrate. By ciliary activity an adhesive secretion is spread over the metamorphosing larva and the attachment area. Two polypides appear through the larval terminal opening. The mantle fold, together with gland cells, nerve cells, sensory cells, and muscle cells from the larva form a nutritive cell mass. Reduction of this nutritive cell mass is accomplished by autolysis and phagocytosis. An invaginated area of the nutritive cell mass is provided with a dense layer of microvilli, which seem to have an absorbtive function. The nutritive cell mass consisting of transitory larval tissues provides a significant source of nutrient for the developing polypide buds.     

On the structure of the pulmonate osphradium

Summary The osphradium of Planorbarius consists of a blindly-ending ciliated canal, formed by an infolding of the mantle epithelium, and a basal ganglion of nerve cells which is comparable in complexity with ganglia of the central nervous system. The distribution of cell types in the osphradial epithelium is specialised so that three regions can be recognised; the ciliated, the secretory and the sensory regions. The basal sensory region of the canal epithelium consists of ciliated cells and is innervated by sensory neurones of the osphradial ganglion. The middle secretory region contains mainly of mucus-secreting cells and the epithelium adjacent to the osphradial aperture of ciliated cells and secretory cells of a second type. The sensory neurones of the osphradial ganglion are bipolar or of a modified monopolar type. Other monopolar neurones, similar to those common in the central nervous system are of non-sensory function. The osphradium of Paludina, although of typical prosobranch form, possesses ciliated pits similar to the single canal of Planorbarius, which may indicate a shared modality of receptor function. A definite function cannot be ascribed to the pulmonate osphradium based on morphological evidence alone.     

Immunolabeled neuroactive substances in the osphradium of the pond snail Lymnaea stagnalis

The osphradium of molluscs is assumed to be a sensory organ. The present investigation in Lymnaea stagnalis has established two ultrastructurally different types of dendrites in the sensory epithelium. Cells immunoreactive to leucine-enkephalin and FMRFamide send processes to the sensory epithelium. These neurons of the osphradial ganglion are thus considered to be part of the sensory system, as are methionine-enkephalin-immunoreactive cells in the mantle wall in the vicinity of the osphradium. The complexity of the osphradial ganglion is further demonstrated by serotonin-immunoreactive neurons innervating the muscular coat around the osphradial canal and methionine-enkephalin-immunoreactive cells sending projections to the central nervous system.     

Development and differentiation of fetal rat sensory ganglia and spinal cord segments in vitro

Summary Fetal spinal ganglia and spinal cord segments with adhering spinal ganglia were explanted on collagen-coated coverslips. They were investigated with enzyme histochemical methods for the existence of hydrolases and dehydrogenases up to 54 days of cultivation.Alkaline phosphatase was located in arachnoid cells and in mantle cells (satellite cells). Butyrylcholinesterase and alpha-glycerophosphate-menadione-tetrazolium reductase were found in mantle cells. Acetylcholinesterase and indoxylesterase were active in the whole neuron; acid phosphatase and alpha-naphthylacetate esterase were restricted to the perikarya.During the process of cell differentiation in vitro alkaline phosphatase decreased in mantle cells. Acid phosphatase became diminished distinctly in spinal ganglion cells. The other neuronal enzymatic activities remained unaltered during the whole period of cultivation. Proliferated Schwann cells were conspicuous by their activity for butyrylcholinesterase. In newly formed myelin sheaths arylsulphatase was active. Lactate dehydrogenase was contained in the perineurium which had developed. Cultures of long duration could contain cytological formations which were reminiscent of sensory end-organs with respect to their enzyme patterns.The enzyme activities of nervous tissues in vitro in their approximation to the situation in situ are discussed.A preliminary report was presented at the 17th Meeting of the Association of German Neuropathologists and Neuroanatomists, in Freiburg, September 1972.The skilled technical assistance of Miss Johanna Sixel and Miss Charlotte Beyer is gratefully acknowledged.     

Ultrastructure of sensory cells on the mantle tentacles of the gastropod Notoacmea scutum

Previous studies have indicated that the mantle margin of the gastropod mollusc Notoacmea scutum is sensitive to chemical, photic, and mechanical stimulation. Here, the ultrastructure of sensory cells on the mantle tentacles of N. scutum is examined by transmission electron microscopy to determine if morphological types of sensory cells can be correlated with known sensory capabilities. The sensory cells of the mantle tentacles are found to be ciliated, primary receptors with subepithelial nuclei. The ciliated sensory endings are concentrated at the tip of the tentacles, but also occur in smaller numbers along the shaft. Ultrastructural differences between cilia form the basis of distinguishing two types of sensory ending. Type 1 sensory endings, which are over 90% of the endings, bar unusual cilia that typically are filled with an electron-dense material. Type 2 sensory endings bear cilia that have a 9 + 2 arrangement of longitudinal elements and thus more closely resemble previously reported sensory cilia of molluscs.     

Morphological,histochemical, and ultrastructural characterization of the accessory cells of neuromasts in the salamander Pleurodeles waltlii

Summary The ultrastructural and histochemical features of the accessory cells of the neuromast of the salamander P. waltlii have been examined. Three types of accessory cells, supporting, mantle, and basal, were found, but only the first 2 are considered in this article. Supporting cells characterized by a highly dilated endoplasmic reticulum occur among and surrounding sensory cells. Mantle cells, morphologically different from the supporting cells, surround the remainder of the neuromast. Both types of accessory cells exhibit histochemically different secretory materials. Our morphological results suggest that both accessory cells contribute to the formation of cupular material.     

Distribution and Ultrastructure of Ciliated Sensory Receptors in the Posterior Mantle Epithelium of Dentalium rectius (Mollusca,Scaphopoda)

The scaphopod mantle cavity opens posteriorly via the pavilion, a siphon-like extension of the posterior mantle through which the respiratory currents pass. The pavilion was examined for ciliated sensory cells in Dentalium rectius Carpenter, 1865, using scanning and transmission electron micropscopy. Three types of sensory receptor were distinguished on the basis of number, length and ultrastructure of the associated cilia. Receptors with 2–5 cilia of ? 1.7 μm length lined the pavilion edge. A second type, possessing 1–2 cilia, ? 8.2 μm in length, was found throughout the internal and on part of the external surface of the pavilion. The third receptor type consisted of a rigid bundle of 16–40 cilia with a length of ? 14.4 μm, and was present close to the periphery and at the base of the pavilion near the entrance to the mantle cavity. The structure and distribution of these cells are similar to peripheral chemo- and mechanoreceptors which sample respiratory currents and the surrounding environment in other molluscs, but they may assume a greater functional significance in scaphopods due to the absence of an osphradium in this class.     

Ultrastructure of the preseptal part of metanephridia in Nais variabilis and Dero digitata (Annelida, Clitellata)

The composition and arrangement of cells in the preseptal region of metanephridia have been examined by ultrastructural methods in two naidid species, Nais variabilis and Dero digitata. Within this region special attention has been paid to the portion around the orifice and the region where the metanephridium penetrates the septum. In N. variabilis, the preseptal region is composed of four cells and, in D. digitata, three cells are present. In both species three cells correspond in position and ultrastructural details and, hence, are interpreted as homologous. These are the mantle cell, the flame cell, and the canal cell. The mantle cell covers the preseptal region and surrounds the opening. The margin around the orifice is endowed with cilia, which extend into the coelomic space and beat irregularly. They do not enter the orifice and, thus, are not part of the internal ciliary flame. Posteriorly, in D. digitata, the mantle cell originates from the septal wall, i.e., its extensions spread in the plane of the frontal coelothelium of the septum. In N. variabilis, the mantle cell is continued by a further cell, enwrapping the posterior region of the preseptal part. This cell, called the septal cell, is anchored in the septal wall like the mantle cell in D. digitata. Both cells are interpreted as mesodermal components of the metanephridium. The flame cell lies beneath the mantle cell. In front, on its dorsal wall, many cilia are inserted which extend posteriorly into the nephridial canal forming a flame. In D. digitata, the caudal extension of this cell was examined in more detail; it originates from an intraseptal position. The canal cell lines the anterior lumen of the nephridial duct. While the mantle cell and flame cell enclose the organ from a dorsal position, the canal cell lies opposite embracing the lumen from a ventromedial position. Behind, it extends into the postseptal region for a certain distance. It is concluded that metanephridia in the Clitellata have a coelothelial component and, probably, are not just descendants of a single cell, the nephridioblast. The results further indicate that a flame cell and a mantle cell or some corresponding coelothelial cells may be constitutive elements of the ground plan of the clitellate metanephridium. Phylogenetic consequences for non-clitellate Annelida are discussed. Accepted: 21 December 1999     

Ultrastructure of the lateral-line sense organs of the ratfish,Chimaera monstrosa

Summary The ultrastructure of the lateral-line neuromasts in the ratfish, Chimaera monstrosa is described. The neuromasts rest at the bottom of open grooves and consist of sensory, supporting, basal and mantle cells. Each sensory cell is equipped with sensory hairs consisting of a single kinocilium and several stereocilia. There are several types of sensory hair arrangement, and cells with a particular arrangement form patches within the neuromast. There are two types of afferent synapse. The most common afferent synapse has a presynaptic body and is typically associated with an extensive system of anastomosing tubules on the presynaptic side. When the tubules are absent, vesicles surround the presynaptic body. These synapses are often associated into synaptic fields, containing up to 35 synaptic sites. The second type of afferent synapse does not have a presynaptic body and is not associated with the tubular system. The afferent synapses of the second type do not form synaptic fields and are uncommon. The efferent synapses are either associated with a postsynaptic sac or more commonly with a strongly osmiophilic postsynaptic membrane. The accessory cells are similar to those in the acoustico-lateralis organs of other aquatic vertebrates. A possibility of movement of the presynaptic bodies and of involvement of the tubular system in the turnover of the transmitter is discussed. A comparison of the hair tuft types in the neuromasts of Ch. monstrosa with those in the labyrinth of the goldfish and of the frog is attempted.     

Fine Structure of the Ampullary Organs of the Bichir Polypterus senegalus Cuvier, 1829 (Pisces: Brachiopterygii) With Some Notes on the Phylogenetic Development of Electroreceptors

The ampullary organs of the bichir were examined by light and electron microscopy. Unlike most other ampullary organs, they are exclusively found in the epidermis and are never sunk into the subepidermal connective tissue. The sensory epithelium consists of sensory cells and supporting cells surrounded by mantle cells. The luminal surface of the sensory cell is provided with a cilium surrounded by several microvilli. In the apical cytoplasm are found numerous mitochondria and microtubules. In the basal part of the cell synaptic sheets or synaptic bodies opposite to afferent nerve endings are frequent.     

A new epidermal ciliary photoreceptive cell type in Plagiostomum lemani (Plathelminthes, Prolecithophora)

 Plagiostomum lemani possesses extremely specialized intraepidermal sensory cells. These obvious photoreceptors, which are not visible with the light microscope, are ciliary aggregations located in an intracellular cavity. The numerous spiralled cilia have the classic 9 × 2 + 2 arrangement at their base and a modified pattern of microtubules apically. The discovered differentiations do not show a connection to the surface. Neither mantle cells nor pigment cells have been found. The structural similarities with other epidermal photoreceptors of species among the different taxa of free-living Plathelminthes are outlined. Besides the larval stages of the taxon Polycladida known so far, the same kind of light-sensing photoreceptive cell has never been described in any other species of the Plathelminthes. Accepted: 16 November 1997     

Ultrastructure of the sensory palps ofTetranchyroderma papii (Gastrotricha,Macrodasyida)

Summary The sensory palps of the macrodasyoid gastrotrichTetranchyroderma papii contain processes from two types of cell: 22–23 bipolar primary sensory cells and two to three support cells. In the proximal region of the palp each sensory cell contains a short ciliary segment with a basal body and from this ciliary segment a longer distal segment lacking axonemal microtubules extends through the major part of the length of the palp. Each support cell process bears microvilli and contains a conspicuous bundle of microtubules running the entire length of the process. The cell bodies of both cell types are situated in the epidermis of the head region. The palps are interpreted as having a chemosensory function. They are considered to be homologous to the posterior cephalic sensory organ ofTurbanella cornuta, but not the head tentacles ofChordodasys antennatus or nematode amphids.     

Cupular organs in two species of Corella (Tunicata: Ascidiacea)

Abstract. Simple cupular organs similar to those described in Ciona intestinalis were observed in Corella eumyota. They consist of a macula containing the cell bodies of 20–30 primary sensory neurons whose cilia project into a dome‐ or finger‐shaped structure, the cupula. Rather than being found in the mantle lining as in C. intestinalis, the organs were located on the atrial surface of the branchial sac. The sensory innervation was examined in whole‐mount preparations using anti‐tubulin immunohistochemistry. Sensory neurons in C. eumyota showed no immunoreactivity with antisera raised against gonadotropin‐releasing hormone (GnRH). A novel, elongated sense organ termed the cupular strand was found in Corella inflata. It has the same basic components as the simple type of cupular organ but consists of a single, long structure containing ～1500 sensory cells. Located on the atrial surface of the branchial sac, it extends along the midline of the dorsal fold, from the gonoduct openings almost as far as the brain. Preparations were examined using optical and electron microscopy. Nerves and cilia were visualized by anti‐tubulin immunofluorescence microscopy. It was possible to follow the sensory axons from the macula of the cupular strand to points where they joined branches of the visceral nerve, which enters a nerve root at the back of the brain. In C. inflata the sensory cell bodies and their axons were immunoreactive not only with anti‐tubulin but also with an antiserum raised against Tunicate I GnRH. There was no immunoreactivity, however, with Chicken II and catfish GnRH antisera. All three GnRH antisera labeled the dorsal strand plexus, a structure associated with production of GnRH in its role as a reproductive hormone. We concluded that the GnRH‐like molecule labeled in sensory neurons differs from the form of GnRH found in the dorsal strand plexus, and may have a different function, perhaps in the neural control of ciliary activity. The function of the cupular organs in species of Corella has not yet been investigated physiologically, but by analogy with such structures in other metazoans, cupular organs are probably hydrodynamic sensors registering local disturbances or changes in water flow through the atrial cavity.     

Neural crest and placode roles in formation and patterning of cranial sensory ganglia in lamprey

Vertebrates possess paired cranial sensory ganglia derived from two embryonic cell populations, neural crest and placodes. Cranial sensory ganglia arose prior to the divergence of jawed and jawless vertebrates, but the developmental mechanisms that facilitated their evolution are unknown. Using gene expression and cell lineage tracing experiments in embryos of the sea lamprey, Petromyzon marinus, we find that in the cranial ganglia we targeted, development consists of placode‐derived neuron clusters in the core of ganglia, with neural crest cells mostly surrounding these neuronal clusters. To dissect functional roles of neural crest and placode cell associations in these developing cranial ganglia, we used CRISPR/Cas9 gene editing experiments to target genes critical for the development of each population. Genetic ablation of SoxE2 and FoxD‐A in neural crest cells resulted in differentiated cranial sensory neurons with abnormal morphologies, whereas deletion of DlxB in cranial placodes resulted in near‐total loss of cranial sensory neurons. Taken together, our cell‐lineage, gene expression, and gene editing results suggest that cranial neural crest cells may not be required for cranial ganglia specification but are essential for shaping the morphology of these sensory structures. We propose that the association of neural crest and placodes in the head of early vertebrates was a key step in the organization of neurons and glia into paired sensory ganglia.     

Ultrastructure of presumptive light sensitive ciliary organs in larvae of Poecilochaetidae,Trochochaetidae, Spionidae,Magelonidae (Annelida) and its phylogenetic significance

Larvae of Poecilochaetus serpens, Trochochaeta multisetosum and Polydora ciliata possess almost identical unpigmented, ciliary, presumptive light sensitive organs within the prostomium. The data corroborate hypotheses on the close relationship of Poecilochaetidae, Trochochaetidae and Spionidae and are even congruent with inclusion of Poecilochaetidae and Trochochaetidae within Spionidae. The organs in P. serpens, T. multisetosum and P. ciliata are composed of one monociliary receptor cell, one supportive cell and several associated flask shaped bipolar sensory cells. The receptor cell cilium enters the supportive cell cavity through a thin pore, dilates and then branches into a high number of disordered projections. The associated sensory cells bear one or occasionally two cilia, which run horizontally beneath or within the cuticle. The supportive cell cavity is not sealed by any cell contact from the subcuticular extracellular space. The organs in Magelona mirabilis are composed of a single supportive cell, but several receptor cells. No further sensory cells are associated. Each receptor cell sends one cilium into an own invagination of the supportive cell, and the ciliary branches are highly ordered. The examined organs in P. serpens, T. multisetosum and P. ciliata exhibit a unique organization amongst polychaetes. The organs of M. mirabilis are most probably homologous. A homology to ciliary organs of Protodrilida is conceivable. In the lineage leading to Protodrilida, primary larval organs may have been integrated into the adult body organization by heterochrony.     

Immunostaining of peripheral nerves and other tissues in whole mount preparations from hatchling cephalopods

Newly hatched paralarvae ("hatchlings") or late-stage embryos of Loligo opalescens were dissected and pieces of tissue removed for immunostaining as flat whole mounts. The general layout of the peripheral nervous system in the mantle and gills was investigated using antisera for tubulin and FMRFamide. Primary sensory neurons are densely distributed in the outer mantle epidermis and show strong FMRFamide immunoreactivity. Their axons form a plexus in the underlying dermis, but do not appear to innervate the chromatophore muscles, which are well visualized with anti-tubulin. Some cross the muscle layer and enter the stellate ganglia via the stellar nerves. The stellate ganglion neuropil contains a rich FMRFamide-immunoreactive mass of axons. It is suggested that these axons originate in large part from sensory neurons in the skin and that the known modulatory effects of FMRFamide-related peptides on motor output of the stellate ganglion may be a reflection of this sensory input in normal life. FMRFamide-immunoreactive primary sensory neurons are also abundant in the gills, but unlike those in the mantle, these cells lack cilia or other external projections. Anti-tubulin staining reveals a network of interstitial cells in the mantle dermis. Such networks may have been mistaken for nerve nets in older accounts. Additional results with Octopus vulgaris hatchlings and immunostaining for serotonin (5HT), small cardioactive peptide (SCP), and gonadotropin releasing hormone (GnRH) are briefly reported.     

Photoreceptors in species of the Macrostomida (Plathelminthes): ultrastructural findings and phylogenetic implications

The submicroscopic anatomy of intracerebral and pericerebral photoreceptors in six species of the Macrostomida is described. Cylindromacrostomum notan-dum, Paramyozonaria simplex and Macrostomum hystricinum marinum possess two rhabdomeric intracerebral photoreceptors each consisting of two pigmented cup cells and three (C. notandum and P. simplex) or two sensory cells (M. hystricinum marinum). In C. notandum and P. simplex two of the sensory cells are equal in size, while the third one is much smaller. This organisation is hypothesised as an autapomorphy of the Dolichomacrostomidae. Photoreceptors with two mantle cells are also known for Microstomum spiculifer. Since only one cup cell exists in representatives of nearly all other high-ranked taxa of the Rhabditophora, it is concluded that the characteristic ”two cup cells in rhabdomeric photoreceptors” has evolved in the stem lineage of the taxon Macrostomida or Macrostomorpha, respectively. In Myozona purpurea and Psammomacrostomum turbanelloides rhabdomeric intracerebral photoreceptors of a special type were encountered. These light-sensing organs consist of numerous cells forming an ellipsoid. The surface membranes of these cells are elongated to form filiform extensions which are tightly intertwined with each other. Pericerebral ciliary aggregations consisting of cells with an internal cavity into which axonemata of modified cilia project were observed in all species mentioned above and in Bradynectes sterreri as well. Such putative light-perceiving organs are widespread within taxa of the Plathelminthes Rhabditophora and have been hypothesised either as homologous characteristics or as analogous ones. With increasing examples being described it becomes likely that pericerebral ciliary aggregations are an apomorphic ground pattern characteristic of the Rhabditophora. Accepted: 22 January 2001