Dynamic tuning of hair bundle mechanoreceptors in a sea anemone during predation

The sea anemone Haliplanella luciae (Cnidaria, Anthozoa) detects chemical and mechanical stimuli from prey. Hair bundle mechanoreceptors on the tentacles participate in regulating discharge of microbasic p-mastigophore nematocysts. Properly stimulated hair bundles sensitize the anemone to discharge nematocysts into objects that contact the tentacles. The hair bundle mechanoreceptors are composed of stereocilia derived from a multicellular complex. This complex consists of a single sensory neuron surrounded by two to four supporting cells. The mechanoreceptor is similar in many ways to vertebrate hair cells of the acousticolateralis system. However, anemone hair bundles are adjustable in structure and responsiveness according to the activity of two different chemoreceptors. One chemoreceptor binds N -acetylated sugars and the other binds amino compounds including proline. N -acetylated sugars induce lengthening of the hair bundle and a downward shift in frequencies that elicit maximal discharge of microbasic p-mastigophore nematocysts. Furthermore, N -acetylated sugars shift maximal discharge to smaller amplitude vibrations. Thus, N -acetylated sugars likely tune hair bundles so that small, swimming zooplankton stimulate maximal discharge. Proline leaks into the seawater from the hemolymph of wounded prey. Proline induces shortening of the hair bundle and shifts maximal discharge of nematocysts to higher frequencies and to larger amplitude vibrations. Thus, proline likely tunes hair bundles so that small, wounded, prey stimulate maximal discharge of nematocysts as they struggle to escape. Thus, suitably sized prey stimulate maximal discharge of microbasic p-mastigophore nematocysts upon first contacting the anemone tentacle and again upon attempting to escape.     

Active Nematocyst Isolation Via Nudibranchs

Cnidarian venoms are potentially valuable tools for biomedical research and drug development. They are contained within nematocysts, the stinging organelles of cnidarians. Several methods exist for the isolation of nematocysts from cnidarian tissues; most are tedious and target nematocysts from specific tissues. We have discovered that the isolated active nematocyst complement (cnidome) of several sea anemone (Cnidaria: Anthozoa) species is readily accessible. These nematocysts are isolated, concentrated, and released to the aqueous environment as a by-product of aeolid nudibranch Spurilla neapolitana cultures. S. neapolitana feed on venomous sea anemones laden with stinging nematocysts. The ingested stinging organelles of several sea anemone species are effectively excreted in the nudibranch feces. We succeeded in purifying the active organelles and inducing their discharge. Thus, our current study presents the attractive possibility of using nudibranchs to produce nematocysts for the investigation of novel marine compounds.     

Nematocysts of Rhopilema nomadica (Scyphozoa: Rhizostomeae), an immigrant jellyfish in the eastern mediterranean

Rhopilema nomadica—a recently discovered scyphomedusa in the eastern Mediterranean—is considered a lessepsian migrant. Its nematocysts were extracted from the scapular and mouth-arm tentacles and examined using light and electron microscopy techniques. The morphometric parameters of the nematocysts were measured before and after complete discharge. Three categories of nematocysts were identified: heterotrichous isorhiza haploneme, holotrichous isorhiza haploneme, and heterotrichous microbasic eurytele. The relative abundance of the nematocysts and their occurrence in tissues of the jellyfish were noted. A brief discussion concerning the classification of certain types of nematocysts is given. A comparison with the available data on other Rhopilema species revealed that the nematocyst categories of R. nomadica are more similar to those of the Atlantic R. verrilli than to those of the Western Pacific R. esculentum. A brief comparison of the injuries caused by these species is given. © 1995 Wiley-Liss, Inc.     

Nematocysts (stinging capsules of Cnidaria) as Donnan-potential-dominated osmotic systems

Isolated nematocysts (capsules of stinging cells in Cnidaria) from the freshwater polyp Hydra vulgaris [Weber, J., Klug, M. & Tardent, P. (1987) Comp. Biochem. Physiol. 88B, 855-862] are under a constant internal osmotic pressure of 12.5 MPa. The capsular wall which withstands this considerable pressure has an average elasticity modulus of approximately 1 GPa, enabling the cyst to swell from its relaxed state to more than double its volume. If the large concentrations of Mg2+ and Ca2+ within isolated nematocysts are substituted by alkali ions, the capsular volume increases by 15% and the final osmotic pressure rises to 15.3 MPa whereas after substitution by Ca2+ a decrease to 90% of the volume and 6.5 MPa is observed. Evidence obtained from the osmotic behavior of nematocysts, as well as data from in vitro exchange of their cations, are consistent with a physicochemical model in which the internal osmotic pressure of nematocysts and thus their ability to discharge is governed by the cationic composition of the content and the salt concentrations in the environment.     

Hydroid defenses against predators: the importance of secondary metabolites versus nematocysts

Marine hydroids are commonly thought to be defended by stinging organelles called nematocysts that penetrate predator tissues and inject proteinaceous venoms, but not all hydroids possess these nematocysts. Although an increasing number of bioactive secondary metabolites have been isolated from marine hydroids, ecological roles of these compounds are poorly known. To test the hypothesis that nematocysts and noxious secondary metabolites represent alternative defenses against predation, we examined hydroids from North Carolina, United States for: (1) the palatability of whole polyps before and after nematocysts had been deactivated; (2) the palatability of their chemical extracts; and (3) their nutritional value in terms of organic content, protein content, and levels of refractory structural material (chitin). All hydroids were avoided by a generalist predator, the pinfish Lagodon rhomboides, compared with palatable control foods. Two of these (Halocordyle disticha and Tubularia crocea) became palatable after being treated with potassium chloride to discharge their nematocysts, suggesting that these species rely on nematocysts for defenses against predators. Chemical extracts from nematocyst-defended species had no effect on fish feeding. The four species that remained unpalatable after nematocysts had been discharged (Corydendrium parasiticum, Eudendrium carneum, Hydractinia symbiolongicarpus, Tridentata marginata) possessed chemical extracts that deterred feeding by pinfish. We have isolated and characterized the structures of the deterrent metabolites in two of these species. We found no differences in nutritional content or levels of chitin between nematocyst-defended and chemically defended species, and no evidence that either of these played a role in the rejection of hydroids as prey. Our results suggest that, among hydroids, chemical defenses may be at least as common as nematocyst-based defenses and that the two may represent largely alternative defensive strategies. The four hydroid species with deterrent extracts represent four families and both sub-orders of hydroids, suggesting that chemical defenses in this group may be widespread and have multiple origins. Received: 25 May 1999 / Accepted: 1 February 2000     

Nematocyst composition of the cubomedusan Chiropsalmus quadrigatuschanges with growth

The nematocysts of Chiropsalmus quadrigatus (Cubozoa; Cubomedusa; Chirodropidae) were examined to determine if their composition changes with an increase in body size. Fixed tentacles of specimens collected in Okinawa, Japan, were homogenized and their nematocysts were observed under a differential interference contrast microscope. Six nematocyst types were observed in medusae of all sizes microbasic mastigophores (MM), large and small trirhopaloids (lTR and sTR), holotrichous isorhizas (HI), ellipsoidal isorhizas (eI), and ovoid isorhizas (oI). Two other nematocysts, large ovoid isorhizas (loI) and microbasic euryteles (ME), were observed only in small individuals. There was also marked difference in proportion of tentacular nematocysts between small and large individuals. HI was the dominant type in small specimens, while MM and eI were predominant in large specimens. Nematocyst composition in the bell and pedalia also differed between small and large individuals. Bells of small medusae contained oI and sTR, while only oI were observed in most large individuals. The pedalia of small medusae had clusters of MM, ME, sTR, and oI. Such single clusters on pedalium bases were characteristic of small individuals. The pedalia of large individuals contained scattered oI. Tentacles of medusae are used for prey capture, so the changes in the major type of nematocysts in tentacles may reflect changes in prey type.     

The utilization of cnidarian nematocysts by aeolid nudibranchs: Nematocyst maintenance and release in spurilla

Some nudibranchs that feed on cnidarians are known to store nematocysts within cnidophage cells and use them for their own defense. Most of the nematocysts are in direct contact with the cytoplasm of the cnidophage. Nematocysts are not subjected to lysosomal enzymes because any phagocytic membrane that surrounded the nematocyst after engulfment does not persist. Cnidophage organelles are restricted to regions surrounding the nematocysts and may aid in the maintenance and development of the nematocysts. The release of cnidophages is initiated by a contraction of a dense muscle complex surrounding the cnidosac. Nematocysts do not discharge if the cnidophage membrane does not rupture upon release. A comparison of nematocyst maintenance in Spurilla neapolitana and nematocyst retention in other organisms is presented.     

Rhythmic sensitization of nematocyst discharge in response to vibrational stimuli

Sea anemones capture prey by discharging nematocysts and other cnidae. Discharge of microbasic p-mastigophore (mpm) nematocysts is regulated in part by hair bundle mechanoreceptors on tentacles arising from multicellular complexes consisting of supporting cells and a sensory neuron. Anemone hair bundles detect movements of prey and then sensitize cnidocytes (cnida-containing cells) to discharge mpm nematocysts in response to contact between the prey and tentacle. Data from a simple bioassay based on counting nematocysts discharged into test probes, indicate that approximately twice as many nematocysts discharge into test probes touched to tentacles after sensitization than before sensitization. We here report that sub-second bursts of vibrational stimuli at key frequencies (51, 55, 65, or 74 Hz; Watson GM, Mire P, Hudson RR. 1998. J Exp Zool 281:582-593) sensitize discharge for at least 90 sec. Very few complete cycles of vibration are sufficient to sensitize discharge. However, as the number of cycles of vibration is increased, discharge is sensitized in rhythmic patterns. Computer analysis of the data by fast Fourier transforms indicates discharge to vibrations at 65 Hz is sensitized every 6.75 cycles. At 51 Hz discharge is sensitized every 2.00 cycles. At 74 Hz, discharge is sensitized in a polyrhythm occurring every 4.26, 3.76, 2.46, and 2. 10 cycles, respectively. At 55 Hz, discharge is sensitized in a polyrhythm occurring every 6.09, 3.20, 2.91, and 2.0 cycles, respectively. Apparently, cells in the neuronal pathway interconnecting anemone hair bundles with cnidocytes count cycles of vibration and then sensitize discharge or not according to the tally. J. Exp. Zool. 286:262-269, 2000.     

Morphology,distribution, and evolution of apical structure of nematocysts in hexacorallia

Cnidae are complex intracellular capsules made by all cnidarians. The most diverse of these capsules are nematocysts, which are made by all members of the phylum; spirocysts and ptychocysts are made only by members of some lineages, and they show less functional and structural diversity. In nematocysts, the apex has been shown to be either a hinged cap (operculum) or three flaps that flex outward during discharge. The operculum is known only from medusozoan nematocysts; flaps are known only from nematocysts of members of the hexacorallian order Actiniaria, although they have been inferred to be characteristic of Anthozoa, the group to which Actiniaria belongs. Using scanning and transmission electron microscopy, we discover a third apical morphology in nematocysts, an apical cap, which we find in all nonactiniarian anthozoans examined. This apical cap is identical structurally to the apical cap of spirocysts, and it resembles the apical structure of ptychocysts, whose apex is documented here for the first time. Additionally, a full survey of nematocysts from all body structures of two actiniarians demonstrates that a particular type of nematocyst, the microbasic p‐mastigophore of the mesenterial filaments, does not have apical flaps. The observed variation does not correspond to conventional categorization of capsule morphology and raises questions about the function and structure of capsules across Cnidaria. Despite some ambiguity in optimization of ancestral states across cnidae, we determine that the apical cap is the plesiomorphic structure for anthozoan cnidae and that apical flaps are a synapomorphy of Actiniaria. At present, the operculum is interpreted as a synapomorphy for Medusozoa, but either it or an apical cap is the ancestral state for nematocysts. J. Morphol. 273:121–136, 2011. © 2011 Wiley Periodicals, Inc.     

The cnidarian nematocyst: a miniature extracellular matrix within a secretory vesicle

Nematocysts are the taxon-defining features of all cnidarians including jellyfish, sea anemones, and corals. They are highly sophisticated organelles used for the capture of prey and defense. The nematocyst capsule is produced within a giant post-Golgi vesicle, which is continuously fed by proteins from the secretory pathway. Mature nematocysts consist of a hollow capsule body in which a long tubule is coiled up that, upon discharge, is expelled in a harpoon-like fashion. This is accompanied by the release of a toxin cocktail stored in the capsule matrix. Nematocyst discharge, which is one of the fastest processes in biology, is driven by an extreme osmotic pressure of about 150 bar. The molecular analysis of the nematocyst has from the beginning indicated a collagenous nature of the capsule structure. In particular, a large family of unusual minicollagens has been demonstrated to form the highly resistant scaffold of the capsule. Recent findings on the molecular composition of Hydra nematocysts have confirmed the notion of a specialized extracellular matrix, which is assembled during an intracellular secretion process to form the most complex predatory apparatus at the cellular level.     

NEMATOCYSTS OF THE SEA ANEMONE METRIDIUM

Six types of nematocysts and their nematocytes in tentaclesand acontia of the sea anemone Metridium senile fimbriatum werestudied by electron microscopy. Microbasic b-mastigophores, microbasic amastigophores, and basitrichshave one fundamental feature in common: a straight, complexly-foldedshaft with dense spines pointing apically. An additional resemblancebetween a b-mastigophore and a basitrich is the possession ofa long, narrow, coiled thread bearing spines. An amastigophoreis characterized by a short, looped, unspined thread and a cup-shapedgranular matrix. Atrich and holotrich nematocysts have a coiled, spined tubeof uniform diameter which lies in an evenly granular matrixfilling the entire capsule. The above five nematocysts have three flaps at the apex of thecapsule which open upon discharge, and each nematocyte possessesa flagellum with which is associated one or two centrioles anda striated rootlet. The long rootlet of the b-mastigophorebearingnematocyte passes through a circular band of fibrils surroundingthe neck region of the capsule, and the short rootlet of theatrich lies in a dense fibrous sheath surrounding all but theapex of the capsule. The spirocyst differs from the other nematocysts in having athin, ridged, singlewalled capsule; an inverted tube containingbundles of tubules; an apical disk covered only by a thin layerof granular material and the nematocyst membrane; and the absenceof a flagellum in its nematocyte. Theories of excitation and mechanism of discharge of nematocystsand the function of spirocysts are discussed in the light ofthis and other recent studies of the fine structure of nematocysts.Special attention is drawn to the probable role of the foldsin the walls of shaft and thread in increasing the length ofthe tube upon discharge.     

Discharge of nematocysts isolated from aeolid nudibranchs

Nematocysts were extracted from 3 nudibranch species and one sea anemone species, and the ability of several test fluids to promote discharge was examined. Except when isolated in sodium citrate, nudibranch nematocysts did not discharge in response to any test fluids. Nudibranch nematocysts isolated in sodium citrate discharged when tested with EGTA, distilled water, and calcium-free artificial seawater, but there were differences among the 3 nudibranch species. Nematocysts isolated from one nudibranch species and nematocysts isolated from that nudibranch's sea anemone prey differed in the percentage that discharged in response to EGTA and distilled water. These results suggest that nematocysts stored by nudibranchs are altered in some way, resulting in the different discharge responses.     

Different nematocytes have different synapses in the sea anemone Aiptasia pallida (Cnidaria,Anthozoa)

Sea anemones feed by discharging nematocysts into their prey, but the pathway for control of nematocyst discharge is unknown. The purpose of this study was to investigate the ultrastructural evidence of neuro-nematocyte synapses and to determine the types of synaptic vesicles present at different kinds of nematocyst-containing cells. The tip and middle of tentacles from small specimens of Aiptasia pallida were prepared for electron microscopy and serial micrographs were examined. We found clear vesicles in synapses on mastigophore-containing nematocytes and dense-cored vesicles in synapses on basitrich-containing nematocytes and on one cnidoblast with a developing nematocyst. In addition, we found reciprocal neuro-neuronal and sequential neuro-neuro-nematocyte synapses in which dense-cored vesicles were present. It was concluded that : (1) neuro-nematocyte synapses are present in sea anemones, (2) different kinds of synaptic vesicles are present at cells containing different types of nematocysts, (3) synapses are present on cnidoblasts before the developing nematocyst can be identified and these synapses may have a trophic influence on nematocyst differentiation, and (4) both reciprocal and sequential synapses are present at the nematocyte, suggesting a complex pathway for neural control of nematocyst discharge. J. Morphol. 238:53–62, 1998. © 1998 Wiley-Liss, Inc.     

A sea anemone's environment affects discharge of its isolated nematocysts

Nematocysts were isolated from individuals of Calliactis tricolor maintained under different feeding schedules or in different salinities in an attempt to determine how these culture conditions influence the discharge of isolated nematocysts. In addition, the discharge frequencies of nematocysts isolated from two different populations of sea anemones found in two different environments were also compared. Undischarged acontial nematocysts were isolated by extrusion into 1 M sodium citrate and were then treated with 5 mM EGTA to initiate discharge. Nematocysts isolated from anemones maintained under three different feeding schedules showed significantly different responses to the test solution. Nematocysts isolated from anemones maintained in two different salinities did not differ significantly in discharge frequency. Nematocysts isolated from individuals from two separate populations of C. tricolor responded significantly differently to 5 mM EGTA and to deionized water, and these responses also depended upon the isolation solution used. Environmental conditions are known to have an impact on the physiological state of most organisms, but this is the first study providing evidence that the environment or feeding state of an anemone affects discharge of isolated nematocysts. Inherent differences in ionic and osmotic characteristics among nematocysts could explain some of the ambiguities when comparing past studies of isolated nematocyst discharge.     

Formation and discharge of nematocysts is controlled by a proton gradient across the cyst membrane

Cnidaria catch and kill their prey by means of nematocysts. A nematocyst consists of a capsule containing a coiled tubule. On triggering, the cyst extrudes this tubule in an extremely rapid manner. The mechanisms and driving forces of discharge are still unknown. We found nematocysts of various cnidarians to be acidic inside and propose that the pH difference between cyst matrix and cytoplasm drives the discharge of cysts. For large cysts of Aiptasia we calculated that the internal concentration of protons and protonated carboxyl groups is about 5 M. Cysts contain polyacids in a high concentration. At a low pH several of the carboxyl groups of the polymer are uncharged. The carboxyl groups dissociate when, on triggering, the proton concentration becomes balanced across the cyst membrane. The speed of protons in water is extremely rapid. Thus, the equilibration of the proton concentration initially results in a negative net charge within the cyst and therefore in a sudden electrostatic repulsion between the dissociated carboxyl groups of the polymer. This causes an increase in the pressure of the matrix against the cyst wall. We suggest that this nonosmotic pressure increase causes the first and extremely rapid step of discharge. We propose that in a second step cations and water are taken up, generating an increase in osmotic pressure. A change in the pH value may also facilitate the invagination and evagination, respectively, of the tubule.     

Inorganic Nutrient Concentrations and Chlorophyll in the Euphotic Zone of Lake Tanganyika

The taxonomic value of nematocyst size in sea anemones is still being assessed. We evaluate size distribution of nematocysts of one type in a single individual anemone. Length of unfired nematocysts was measured along the column, tentacles, and actinopharynx of a preserved specimen of Actinodendron arboreum (Quoy & Gaimard, 1833). Mean, range, minimum, and maximum length of nematocysts vary along the column, those in the middle region being least variable. The length of nematocysts in mature (split) acrospheres is less variable than in immature (unsplit) acrospheres. There is significant variability between nematocysts in tentacles of the primary and quaternary cycles, and along a tentacle, the middle being least variable. Size distribution of actinopharynx nematocysts is complex. The results of this study suggest that assembling data on nematocysts from multiple individuals for taxonomic purposes should be used with an awareness that sampling site can be an important variable. Ideally, the position of tissue sampled should be documented, an attempt should be made to be consistent in sampling from the same position in individuals being compared, and the variability of nematocyst length at each sampled site should be assessed. Inferences can also be made on ontogeny from these data; we conclude that an actinodendrid tentacle grows from the base and at the tips of its branches.     

A modified view on octocorals: Heteroxenia fuscescens nematocysts are diverse, featuring both an ancestral and a novel type

Cnidarians are characterized by the presence of stinging cells containing nematocysts, a sophisticated injection system targeted mainly at prey-capture and defense. In the anthozoan subclass Octocorallia nematocytes have been considered to exist only in low numbers, to be small, and all of the ancestral atrichous-isorhiza type. This study, in contrast, revealed numerous nematocytes in the octocoral Heteroxenia fuscescens. The study demonstrates the applicability of cresyl-violet dye for differential staining and stimulating discharge of the nematocysts. In addition to the atrichous isorhiza-type of nematocysts, a novel type of macrobasic-mastigophore nematocysts was found, featuring a shaft, uniquely comprised of three loops and densely packed arrow-like spines. In contrast to the view that octocorals possess a single type of nematocyst, Heteroxenia fuscescens features two distinct types, indicating for the first time the diversification and complexity of nematocysts for Octocorallia.     

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.     

Evidence for involvement of TRPA1 in the detection of vibrations by hair bundle mechanoreceptors in sea anemones

A homolog of TRPA1 was identified in the genome of the anemone, Nematostella vectensis (nv-TRPA1a), and predicted to possess six ankyrin repeat domains at the N-terminus and an ion channel domain near the C-terminus. Transmembrane segments of the ion channel domain are well conserved among several known TRPA1 polypeptides. Inhibitors of TRPA1 including ruthenium red decrease vibration-dependent discharge of nematocysts in N. vectensis and Haliplanella luciae. Activators of TRPA1 including URB-597 and polygodial increase nematocyst discharge in the absence of vibrations. Co-immunoprecipitation yields a band on SDS-PAGE gels at the predicted mass of the nv-TRPA1a polypeptide among other bands. Co-immunoprecipitation performed in the presence of antigenic peptide decreases the yield of this and several other polypeptides. In untreated controls, anti-nv-TRPA1a primarily labels the base of the hair bundle with some labeling also distributed along the length of stereocilia. Tissue immunolabeled in the presence of the antigenic peptide exhibits reduced labeling. Activating chemoreceptors for N-acetylated sugars induce immunolabel to distribute distally in stereocilia. In anemones, activating chemoreceptors for N-acetylated sugars induce hair bundles to elongate among several other structural and functional changes. Taken together, these results are consistent with the possibility that nv-TRPA1a participates in signal transduction of anemone hair bundles.     

Calcium- and voltage-dependence of nematocyst discharge in Hydra vulgaris

In Hydra vulgaris, discharge of stenotele nematocysts was induced by contact with prey, electrical stimuli, or increase in the external potassium concentration. In each case 10^-4 M calcium was required in the culture medium. The results indicated a voltage- and calcium-dependent mechanism different from mechano- or chemoreception allowing calcium influx from the external medium. A threshold for activation was suggested by the steep increase of the rate of electrically induced discharge in external fields of 3.5 kV/m. Although organic antagonists for vertebrate calcium channels were ineffective in blocking the calcium-induced nematocyst discharge, inorganic divalent and trivalent cations competitively inhibited the process, with a sequence (Co²⁺ < Ni²⁺ < Cd²⁺ < La³⁺ < Gd³⁺) similar to that seen for antagonism of calcium influx through voltage-dependent channels. Magnesium, an intracellular calcium antagonist, decreased nematocyst discharge, while strontium replacing calcium supported the discharge at a lowered rate. It is concluded that in the nematocyte a voltage-activated influx of calcium through apical ion channels initiates the discharge of the nematocyst in an exocytotic process.