Apical surface of hydrozoan nematocytes: Structural adaptations to mechanosensory and exocytotic functions

At the apical cell pole of the nematocytes of a hydrozoan (Hydra vulgaris), cytoskeletal elements of different molecular families (microfilaments, microtubules, cross-striated rootlets) are combined in a complex framework. As determined by transmission and scanning electron microscopy, the stimulus-transducing cnidocil apparatus of these mechanosensitive cells is forced into a lateral position, facilitating the close apposition of the nematocyst to the apical cell membrane. The nematocyst, a single, extraordinarily large, exocytotic organelle, is held in position by a microtubular basket. The cnidocil apparatus and microtubular basket are linked to an ellipsoid arrangement of pseudovilli, i.e., small surface protrusions containing cross-striated rods. These nematocyte-specific, cytoskeletal elements mediate the anchorage of the entire cytoskeletal framework to the apical cell membrane. The apical membranes of the nematocyte and nematocyst are separated by a distance of only ～ 50 nm. Structural modifications on the external side of the cyst membrane resemble those of synaptic membranes. © 1994 Wiley-Liss, Inc.     

The ciliated sensory cell of Stauridiosarsia producta (Cnidaria,Hydrozoa) — a nematocyst-free nematocyte?

Summary A mechanosensitive ciliated cell type of the polyp Stauridiosarsia producta (Hydrozoa) was investigated by means of electron microscopy. These cells bear at their apical cell surface a modified cilium, a set of seven stereovilli, a so-called pseudovillar system and a large vacuole. Cilium and stereovilli are interconnected like the cnidocil apparatus of hydrozoan nematocytes which is responsible for mechanoelectric transduction. The vacuole is enclosed by and linked to the pseudovillar system by a microtubular basket. Considering its structural organization and physiological activities the ciliated sensory cell closely resembles a nematocyte that has lost its ability ot produce a nematocyst.     

Arrangement of accessory cells and nematocytes bearing mastigophores in the tentacles of the cubozoan Chironex fleckeri

Nematocytes containing microbasic mastigophores are intimately associated with accessory cells in the epidermis of Chironex fleckeri. Large microbasic mastigophores may be surrounded by seven to nine such cells. Each accessory cell possesses an apical portion containing secretory droplets and a basal portion which carries a radially oriented fibre linking the cell to the underlying mesogloea. The fibre is capable of projecting and retracting the accessory cell. Junctional complexes occur between accessory cells and the apical regions of neighbouring mastigophores. Each nematocyte bearing a mastigophore contains a triggering apparatus consisting of a cnidocil surrounded by microvilli. This apparatus protrudes from an invagination in the apical region of the nematocyte and is exposed when the mastigophore is in the fire-ready position. A basket of filaments which make contact with microvilli surrounds the apical end of the nematocyst like a collar. The basket is linked via fibrous bundles which envelop the mastigophore to radially oriented fibres basally. These fibres are capable of projecting and retracting the mastigophore and its associated triggering apparatus. Up to nine such fibres were observed to be associated with a single large microbasic mastigophore. Microtubules averaging 25 nm in diameter and linked via cross bridges to electrondense material were detected in the radial fibres of both nematocytes and accessory cells. Retraction of the accessory cells and projection of nematocytes result in mastigophores being brought to the firing line and in the exposure of the cnidocil apparatus.     

Anchorage and retraction of nematocytes in the tentacles of the cubopolyp Carybdea marsupialis are mediated by a species-specific mesogleal support

Each tentacle of the cubopolyp Carybdea marsupialis is armed with only a single nematocyte at its tip. The correct position of the nematocyte is maintained by a crown-shaped cup formed by the mesoglea. In maximally contracted tentacles, the nematocyte and 7–10 surrounding accessory cells are completely retracted into an ectodermal invagination. A belt of muscle cells revealing a distinct cross-striation in specimens labelled with fluorescein-isothiocyanate-phalloidin is located around the basal part of the nematocyte. These muscle cells are linked both to the mesogleal cup and to the nematocyte by specialized desmosomal contact zones. An additional set of long slender muscle strands runs through the complete length of the tentacles. Their myofibrils reveal only a weak striation pattern. Whereas the contraction of the tentacles seems to depend on the slender muscle strands, the retraction of the apical cell complex is thought to be mediated by the cross-striated muscle belt.     

Cytological Studies of the Nematocysts of Hydra : II. The Stenoteles

Entire hydras or tentacles were prepared for electron microscopy as described in the preceding paper. The stenotele capsule has been observed to be composed of an external membrane, a thick chitinous or keratin layer, and an inner membrane. A sac-like extension of the capsular wall into the capsule bears spines and stylets on its inner surface and evagination of this structure occurs on discharge. Profiles of tubular or membranous structures often are seen within the capsules of resting stenoteles. These structures are presumably related to the external filament. The spines often reveal a flattened aspect which suggests that at least some of them might more accurately be called "vanes." A cnidocil has been found to accompany each stenotele. This study revealed several aspects of the developmental stages of stenoteles: A vacuole is formed which is nearly surrounded by the nematocyte nucleus. The vacuole content changes in density and a capsular wall is formed at the periphery of the vacuole. Tubules differentiate from the capsular matrix, and spines and stylets develop somewhat later. An operculum is formed from the nematocyte cytoplasm.     

Cytological studies of the nematocysts of Hydra. II. The stenoteles

Entire hydras or tentacles were prepared for electron microscopy as described in the preceding paper. The stenotele capsule has been observed to be composed of an external membrane, a thick chitinous or keratin layer, and an inner membrane. A sac-like extension of the capsular wall into the capsule bears spines and stylets on its inner surface and evagination of this structure occurs on discharge. Profiles of tubular or membranous structures often are seen within the capsules of resting stenoteles. These structures are presumably related to the external filament. The spines often reveal a flattened aspect which suggests that at least some of them might more accurately be called "vanes." A cnidocil has been found to accompany each stenotele. This study revealed several aspects of the developmental stages of stenoteles: A vacuole is formed which is nearly surrounded by the nematocyte nucleus. The vacuole content changes in density and a capsular wall is formed at the periphery of the vacuole. Tubules differentiate from the capsular matrix, and spines and stylets develop somewhat later. An operculum is formed from the nematocyte cytoplasm.     

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.     

Myoanatomy of <Emphasis Type="Italic">Barentsia discreta</Emphasis> (Busk, 1886) (Kamptozoa: Coloniales)

The anatomy of the muscular system of Barentsia discreta (Kamptozoa) was studied by confocal laser scanning and transmission electron microscopy. The calyx musculature, muscles associated with the digestive tract, atrial ring muscles, and tentacle muscles are described. The structure of the muscular bulbus located in the upper part of the stalk and the muscle base of the stalk were examined. The middle part of the stalk and the stolon lack musculature. The structure of the star-cell complex lying at the boundary of the stalk and calyx was examined in detail. Emschermann’s (1969) opinion was confirmed that the star-cell complex performs the function of a heart, providing the transport of substances from the calyx to the stalk and stolon. The general plan of the muscle arrangement is similar in all Kamptozoa; it consists of central muscles of the calyx, atrial ring muscles, tentacle muscles, and muscles associated with the digestive tract. Oral, lateral, and aboral muscles extending from the stalk into the calyx, which were described for solitary forms, are lacking in the calyx of colonial B. discreta. The calyx of B. discreta is separated from the stalk by a septum, through which muscles do not penetrate from the stalk.     

Cellular structure and ultrastructure of the black coral Antipathes aperta: 1. Organization of the tentacular epidermis and nervous system

The tentacular epidermis of the black coral Antipathes aperta is organized into three distinct regions, containing at least nine different types of cells. The outermost region is dominated by spirocytes along with two types of nematocytes, organized into discrete wart-like batteries. The two nematocyte types both contain microbasic b-mastigophore nematocysts. The outer boundary of the wart is marked by the presence of both spumous and vesicular mucus cells. The ciliation of the wart is contributed principally by the spirocytes. Warts are enveloped and separated from one another by an unusual neurosensory cell complex that extends from the tentacular surface to the mesogleal connective tissue foundation. Funnel-like, flagellated cells composing the complex connect with ganglion cells composing the dominant portion of the nerve net system. Branches of this complex also penetrate the central portion of the wart, making direct contact with the cnidae. The tentacular mid-region is composed of nematocytes and spirocytes in various stages of maturation, along with epitheliomuscular cell (EMC) somata. The EMC's narrow apically extend toward the tentacle surface, forming contacts with the cnidae. The basal end of the EMC expands to form the larger portion of the tentacular musculature. The inner region of tentacular epidermis is marked by a neuromuscular complex sheathed by extensions of mesoglea. The ganglion cells occur as a plexus deep within the tentacle and form polarized junctions with the EMC's, but neuromuscular synapses are not well enough defined for documentation. Polarized synapses lacking well-defined membrane thickenings characterize the interneuronal junctions. Granular cells lining the mesogleal surface appear to be responsible for mesogleal fibrillogenesis.     

Ultrastructural evidence for the occurrence of three types of mechanosensitive cells in the tentacles of the cubozoan polypCarybdea marsupialis

Summary The ectodermal cell layer in the tentacles of the cubozoan polypCarybdea marsupialis contains four types of cells (types 1–4) bearing specialized cilia. Epitheliomuscular cells (type 1) are characterized by motile cilia with dynein-decorated axonemes. 200 nm long extramembranous filaments of unknown function are restricted to a belt-like region distal to the transition zone. Up to 40 rn long rigid cilia formed by a slender epithelial cell type (type 2) are surrounded by rings of short microvilli. The axonemes of these cilia are composed of incomplete microtubules and lack dynein. Microvilli and cilia are linked by intermembrane connectors. Microtubuledoublets and ciliary membrane are interconnected by microtubule-associated cross-bridges only within this contact region. At the tip of each tentacle a single nematocyte (type 3) is surrounded by 7–10 accessory cells (type 4). These both cell types are equipped with similar cilium-stereovilli-complexes consisting of a cone-like arrangement of stereovilli and a modified cilium. The axonemal modifications of the cilium, its interconnections with the surrounding stereovilli and the linkages between ciliary axoneme and ciliary membrane are similar to those known from the cnidocil-complexes of hydrozoons and other epithelial mechanosensitive cells of the collar-receptor type. Our data indicate that besides the nematocyte two other types of mechanosensory cells (types 2 and 4) are integrated in the ectodermal cell layer ofCarybdea which possibly affect the triggering mechanism of nematocyst discharge.     

Cytoskeleton-membrane interactions in the cnidocil complex of hydrozoan nematocytes

Summary Each cnidocil complex of the hydrozoans Tubularia larynx and Hydra vulgaris consists of 9 or 7–10 large stereovilli (=stereocilia), respectively, and a modified cilium, the cnidocil. The cnidocils comprise the regular 9 microtubule doublets, up to 30 additional microtubules, as well as a central filament body. Adjacent stereovilli are linked together by intermembrane connectors forming the stereovillar cone. The distal tips of the stereovilli surround the cnidocil in a closed tubular arrangement measuring up to 0.7 m in length. Within this contact region the cnidocil is linked to the stereovillar tube by another set of intermembrane connectors, which seem to hold the cnidocil in a central position within the stereovillar cone. Stereovillar membrane and actin core are linked by 16-nm long cross bridges, which display a periodicity of 16 nm and emerge from the actin core. Within the cnidocils periodically arranged membrane-cytoskeleton bridges are uniformly restricted to the contact region. Here, 24-nm long cross bridges, which are spaced by a regular distance of 20 nm, interconnect the A-tubules of the microtubule doublets and the membrane. The cnidociliary membrane is differentiated into distinct domains as revealed by freeze-fracturing. Within the contact region of the nematocytes of Tubularia larynx, intramembrane particles are arranged in 9 rows of 700 nm length and 50 nm width, separated by particlefree areas. Intramembrane particles are irregularly distributed distal to the contact region. Considering recent physiological results we presume that the latter represent chemoreceptor units, while mechanical stimuli are transmitted via the intermembrane connectors and the microtubule-membrane bridges to mechanosensitive channels within the domain of the cnidociliary membrane in the contact region.     

Functional design of tentacles in squid: linking sarcomere ultrastructure to gross morphological dynamics

This paper offers a quantitative analysis of tentacle extension in squid that integrates several levels of structural organization. The muscular stalks of the two tentacles of squid are rapidly elongated by 70 per cent of resting length during prey capture. A typical duration of the extension is 30 ms in Loligo pealei (with a contracted tentacle length of 93 mm and a strike distance of about 37 mm). In a successful strike, the terminal clubs hit the prey and attach to it via arrays of suckers.A forward dynamics model is proposed for the extension of the tentacular stalk and the forward motion of the terminal club. The stalk is modelled as a longitudinal array of thin muscular discs with extensor muscle fibres oriented parallel to the disc planes. As a disc contracts radially, it lengthens because its volume is constant. The equations of motion for the linked system of discs were formulated and solved numerically. The inputs of the model are the dimensions of the tentacle, passive and active muscle properties such as Hill''s force–velocity relationship, myofilament lengths and activation of the muscle fibres. The model predicts the changing geometry of the tentacle, the pressure and stress distribution inside the tentacle and the velocity and kinetic energy distribution of the stalk and club. These predictions are in agreement with kinematic observations from high-speed films of prey capture. The model demonstrates also that the unusually short myosin filaments (reported range 0.5–0.9 micrometre) that characterize the extensor muscles are necessary for the observed extension performance. Myosin filament lengths typical for vertebrate sarcomeres (1.58 micrometre) would lead to a significant reduction in performance. In addition, the model predicts that, to maximize peak velocity of the terminal club, the myosin filaments should be longer at the base and shorter at the tip of the stalk (0.97 micrometre at the base and 0.50 micrometre at the tip for the tentacle size above). This results from differences in dynamic loading along the stalk. Finally, the model allows exploration of the effects of changes in the dimensions and mass of the tentacle and intrinsic speed of the myofilaments on the optimum myosin filament lengths.     

Ultrastructural analysis of nematocyte removal in Hydra

A consecutive series of ultrathin sections through the distal one-third of a Hydra tentacle has revealed at least four categories of nematocytes: (1) normal, mounted nematocytes, in specific arrangements within the battery cells; (2) degenerating nematocytes, within the battery cells; (3) mature nematocytes, enclosed within endodermal cells; (4) a mature nematocyte, in the enteric cavity. The degenerating nematocytes within the battery cells and the nematocytes in the endoderm and enteric cavity appeared to be aging nematocytes undergoing death and removal. The results provide the first ultrastructural evidence for nematocyte degeneration within battery cells and also suggest phagocytosis of mature nematocytes by endodermal cells.     

Rapid exocytosis of stenotele nematocysts in Hydra vulgaris

Each cnidarian nematocyte includes a vesicular organelle, called nematocyst, which discharges its content when the cell receives appropriate stimuli. Extracellular electrical stimuli induced discharge of in situ stenoteletype nematocysts in Hydra vulgaris when the apical membrane of nematocytes was depolarized by about 25 mV or more (threshold). Stimuli hyperpolarizing the apical membrane induced discharge only at high amplitudes, adding about 80 mV or more to the resting membrane potential of the nematocyte (resulting in a voltage that may permeabilize the apical membrane). In order to determine the speed of the initiating (exocytotic) process, the delay between stimulus and a clearly visible sign of discharge (i.e., protrusion of the nematocyst's stylets) was measured using video microscopy with triggered flash illumination. The minimal delay was 330–450 s and 230–350 s for depolarizing and large hyperpolarizing stimuli, respectively. With depolarizing stimuli, all discharges of stenoteles occurred between 330 and 950 s after the stimulus. The deviation was caused by differences in the physiological state of the animals tested rather than by variance in the responsiveness of different stenoteles in the same tentacle.Voltage dependence, short latency and Ca/Mg-antagonism are similar to those characterizing exocytosis of synaptic vesicles. This correspondence suggests that discharge of nematocysts is initiated by a similar exocytotic process preceding the ejection of the nematocyst's content.     

Ordered progression of nematogenesis from stem cells through differentiation stages in the tentacle bulb of Clytia hemisphaerica (Hydrozoa, Cnidaria)

Nematogenesis, the production of stinging cells (nematocytes) in Cnidaria, can be considered as a model neurogenic process. Most molecular data concern the freshwater polyp Hydra, in which nematocyte production is scattered throughout the body column ectoderm, the mature cells then migrating to the tentacles. We have characterized tentacular nematogenesis in the Clytia hemisphaerica hydromedusa and found it to be confined to the ectoderm of the tentacle bulb, a specialized swelling at the tentacle base. Analysis by a variety of light and electron microscope techniques revealed that while cellular aspects of nematogenesis are similar to Hydra, the spatio-temporal characteristics are markedly more ordered. The tentacle bulb nematogenic ectoderm (TBE) was found to be polarized, with a clear progression of successive nematoblast stages from a proximal zone (comprising a majority of undifferentiated cells) to the distal end where the tentacle starts. Pulse-chase labelling experiments demonstrated a continuous displacement of differentiating nematoblasts towards the tentacle tip, and that nematogenesis proceeds more rapidly in Clytia than in Hydra. Compact expression domains of orthologues of known nematogenesis-associated genes (Piwi, dickkopf-3, minicollagens and NOWA) were correspondingly staggered along the TBE. These distinct characteristics make the Clytia TBE a promising experimental system for understanding the mechanisms regulating nematogenesis.     

Collar cells in planula and adult tentacle ectoderm of the solitary coral Balanophyllia regia (anthozoa eupsammiidae)

Summary The planula larva of the solitary coral Balanophyllia regia has an ectoderm of flagellate, diplosomal collar cells. The collar of these cells is composed of a ring of microvilli linked with mucus strands. Four types of flagellate gland cells, three types of nematocyst and spirocysts are present in the planula ectoderm. The function of these ectoderm cells is discussed. The mesogloeal muscular and packing tissues of the planula are briefly described. The tentacle of the adult coral, examined for comparison, has an ectoderm of flattened flagellate cells with a shallow collar. Collar cells similar to those of the planula are occasionally found on the tentacle and their function is not known. Independent sensory cells built on a modified collar cell plan with collar of thickened microvilli are common in the tentacle. These are quite separate from the three kinds of tentacular nematocyte. Distended glandular areas occur in the tentacle ectoderm. The flagellate tentacle gastrodermis, muscle and mesogloeal region are briefly described. The evolutionary significance of collar cell ectoderm in a planula is discussed and the occurrence of collar cells throughout the animal kingdom, reviewed.I am most grateful to Paul Tranter of the Plymouth Laboratory for providing material and to Gareth Morgan for assistance with electron microscopy.     

Myoanatomy and serotonergic nervous system of plumatellid and fredericellid phylactolaemata (lophotrochozoa,ectoprocta)

The phylogenetic position of the Ectoprocta within the Lophotrochozoa is discussed controversially. For gaining more insight into ectoproct relationships and comparing it with other potentially related phyla, we analysed the myoanatomy and serotonergic nervous system of adult representatives of the Phylactolaemata (Plumatella emarginata, Plumatellavaihiriae, Plumatella fungosa, Fredericella sultana). The bodywall contains a mesh of circular and longitudinal muscles. On its distal end, the orifice possesses a prominent sphincter and continues into the vestibular wall, which has longitudinal and circular musculature. The tentacle sheath carries mostly longitudinal muscle fibres in Plumatella sp., whereas F. sultana also possesses regular circular muscle fibres. Three groups of muscles are associated with the lophophore: 1) Lophophoral arm muscles (missing in Fredericella), 2) epistome musculature and 3) tentacle musculature. The epistome flap is encompassed by smooth muscle fibres. A few fibres extend medially over the ganglion to its proximal floor. Abfrontal tentacle muscles have diagonally arranged muscle fibres in their proximal region, whereas the distal region is formed by a stack of muscles that resemble an inverted ‘V’. Frontal tentacle muscles show more variation and either possess one or two bases. The digestive tract possesses circular musculature which is striated except at the intestine where it is composed of smooth muscle fibres. The serotonergic nervous system is concentrated in the cerebral ganglion. From the latter a serotonergic nerve extends to each tentacle base. In Plumatella the inner row of tentacles at the lophophoral concavity lacks serotonergic nerves. Bodywall musculature is a common feature in many lophotrochozoan phyla, but among other filter feeders like the Ectoprocta is only present in the ‘lophophorate’ Phoronida. The longitudinal tentacle musculature is reminiscent of the condition found in phoronids and brachiopods, but differs to entoproct tentacles. Although this study shows some support for the ‘Lophophorata’, more comparative analyses of possibly related phyla are required. J. Morphol., 2011. © 2011 Wiley Periodicals, Inc.     

Receptor potentials and action potentials in Drosera tentacles

Summary Voltage fluctuations identified as receptor potentials can be detected with electrodes applied to the mucilage surrounding the head of a tentacle of Drosera intermedia if the head is stimulated by contact with a live insect, by the touch of a clean, inert object, or by application of salt solutions. Associated with a low receptor potential are action potentials, which occur at a frequency dependent on the magnitude of the receptor potential. These action potentials can be detected with electrodes applied to any region of the stalk of the tentacle. Inflection of the lower stalk follows the occurrence of action potentials. Inflection is minute for isolated action potentials but large and rapid when several occur within a brief interval.The apparent amplitude of action potentials recorded from the stalk is independent of receptor potential amplitude, but that of action potentials recorded from the mucilage commonly decreases as the receptor potential deviates from the baseline and increases as it returns. It is suggested that variation of apparent amplitude of the action potentials may result from postulated variation in the resistance of receptor membranes.