Organization of the nervous system of physonectid siphonophores

Summary An antiserum to the sequence Arg-Phe-amide (RFamide) was used to stain the nervous systems of various physonectid siphonophores. In the stem of Nanomia bijuga, this antiserum stained an ectodermal nerve net, which was interrupted, at regular intervals, by transverse collars of neurons. Injection of Lucifer yellow into the giant axon of the stem showed that this axon was dye-coupled to an ectodermal nerve net that resembled the RFamide-positive network. Ectodermal nets of neurons were also found in the pneumatophore, gastrozooids, tentacles and tentilla. At the junctions of the pneumatophore, the gastrozooids, the dactylozooids and the gonozooids with the stem, and at the junctions of tentacles and tentilla, collars or rings of neurons occurred. The stem was connected to the phyllozooids and nectophores by muscular lamellae, which were bordered by chains of neurons. At the margin of the nectophores, an immunoreactive nerve ring was found. Connected to this ring and located in theseitliche Zapfen (sidely-located patche), were two agglomerations of nerve cells. On the upper side of the bell margin, positioned at 90° relative to the seitliche Zapfen, a delta-shaped neuronal structure was found. This structure was connected to the nerve ring and was associated with a muscle, which ran a short distance along the exumbrellar surface.The nervous systems of Agalma elegans, Forskalia edwardsi, Forskalia leuckarti and Halistemma rubrum resembled that of Nanomia bijuga in all major respects.     

Arachidonic acid and the control of body pattern inHydra

Summary Repeated stimulation ofHydra magnipapillata with the diacylglycerol (DG) 1,2-sn-dioctanoylglycerol (diC₈) induces an increase in positional value and eventually the development of ectopic heads. Upon stimulation, the polyps release [¹⁴C]-arachidonic acid from previously labelled endogenous sources. Arachidonic acid (AA) is not released into the external medium but remains within the animal, AA, linoleic acid and their lipoxygenase products were identified by gas chromatography-mass spectrometry. Several metabolites were found, most abundantly 12-HETE (hydroxy-eicosa-tetraenoic acid), 8-HETE, 9-HODE (hydroxy-octadecadienoic acid), and 13-HODE; this is the first evidence of their presence in coelenterates. Externally applied AA causes ectopic head formation, though less effectively than diC₈. When administered simultaneously, (diC₈) and AA, which both are known to activate protein kinase C (PKC), act synergistically in inducing ectopic head formation. Since released endogenous AA can spread in tissues, it may mediate a temporal and spatial extension of PKC activation and, hence, broaden the range in which positional value increases. However, in addition to the activation of PKC, the generation of AA metabolites appears to be essential for the induction of ectopic head formation, since not only a selective inhibitor of PKC, chelerythrine, but also an inhibitor of lipoxygenases, NDGA (nordihydroguaiaretic acid), significantly reduces the effectiveness of both AA and DG. Correspondence to: W.A. Müller     

Signal transmission and covert prepattern in the metamorphosis of Hydractinia echinata (Hydrozoa)

Summary Planulae are simply structured larvae lacking an overt longitudinal organization. In the course of a rapid metamorphosis, however, they transform into polyps, which display striking structural patterns. Metamorphosis takes place only in response to external stimuli. Surgical removal and transplantation of larval parts reveal that external stimuli, including artificial inducers such as cesium ions, tumor promoters and diacylglycerol, act on the anterior quarter of the larva where sensory cells containing Arg-Phe-amide-like peptides are located. The external stimuli initiate the release of an internal signal, which is transmitted to the posterior end causing the successive transformation of larval into adult tissue. The transformation front moves from the anterior to the posterior quarter in 60 min. The internal signal can be released or bypassed by a transitory lowering of the Mg²⁺ content of the seawater. By using this procedure, or by administering an extract containing the putative internal signal substance, each isolated part of the larva can be induced to metamorphose separately. Provided there is no time for regeneration after cutting before metamorphosis is initiated, the most anterior fragment forms only stolons, the most posterior fragment forms only a head. The overt pattern of the polyp is, therefore, generated under the influence of a covert anterior-posterior prepattern of the larva.     

Polyp morphogenesis in a scyphozoan: Evidence for a head inhibitor from the presumptive foot end in vegetative buds ofCassiopeia andromeda

Summary Buds ofCassiopeia andromeda have been transected into fragments of various sizes. Depending on their original position in the organism, on their size and on the age of the dissected buds, the fragments either regenerated or developed to a solitary polyp's head without stalk and peduncle. Generally, basal fragments tended to regenerate complete buds, young apical parts mostly differenciated polyp heads whereas apical and middle parts of progressively older buds regenerated buds with increasing frequency. To explain the alteration of the developmental capacities a head inhibitor is postulated which originates from the basal end of the buds and which expands towards the apical pole with increasing age of the buds.     

Immunocytochemical evidence for an NMDA1 receptor subunit in dissociated cells of<Emphasis Type="Italic"> Hydra vulgaris</Emphasis>

We have previously reported immunocytochemical, biochemical, behavioral, and electrophysiological evidence for glutamatergic transmission through (±)--amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid (AMPA)/kainate receptors in hydra. We now report specific localization of the N-Methyl-D-aspartic acid receptor subunit 1 (NMDAR1) in epithelial, nerve, nematocytes, and interstitial cells of hydra. Macerates of tentacle/hypostome pieces of Hydra vulgaris were prepared on agar-coated slides, fixed with buffered formaldehyde/glutaraldehyde, and fluorescently labeled with monoclonal antibodies against mammalian NMDAR1. Negative controls omitted primary antibody. Digital images were recorded and analyzed. Specific localized and intense labeling was found in ectodermal battery cells, other epithelial cells, nematocytes, interstitial cells, and sensory and ganglionic nerve cells, and in battery cells was associated with enclosed nematocytes and neurons. The labeling of myonemes was more diffuse and less intense. In nerve and sensory cells, punctate labeling was prominent on cell bodies. These results are consistent with our earlier evidence for glutamatergic neurotransmission and kainate/NMDA regulation of stenotele discharge. They support other behavioral and biochemical evidence for a D-serine-sensitive, strychnine-insensitive, glycine receptor in hydra and suggest that the glutamatergic AMPA/kainate-NMDA system is an early evolved, phylogenetically old, behavioral control mechanism.     

The distribution of nerve cells inHydra attenuata Pall.

Summary Polyps ofHydra attenuata Pall. were subdivided into four axial fragments (I–IV) of about identical length. Ecto- and endoderm of each of these fragments were separated from each other and dissociated according to the technique of David (1973). Each preparation was qualitatively and quantitatively examined as to its content of nerve cells.The presence of 11 different types of nerve cells (Tardent and Weber, 1976) could be confirmed. While multipolars (M₁, M₂), symmetrical bipolars (B₁, B₂) and unipolars (U₁, U₂) were found in both layers, asymmetrical bipolars (B_3–7) are limited to the endoderm (Fig. 1), which, as a whole, contains fewer nervous elements than the ectoderm (Fig. 2). The ecto- and endoderm of the tentacles could not be separated from each other and the dissociation was only partly successful. It was, however, possible to ascertain that among the nerve cells present in the tentacles the most numerous are the symmetrical bipolars (B₁, B₂).Dr. Epp was awarded a grant of the Swiss National Science Foundation (Nr. 880.480.76). This work was also supported by grant Nr. 3.548.75 of the same Foundation. The authors are indebted to Mr. Chr. Weber for his technical help and advice     

Evidence for new catecholamines or related amino acids in some invertebrate sensory neurons

Summary In certain sensory neurons of many different invertebrate species, including the sea anemones. Metridium senile and Tealia felina and the crustacean Anemia salina, fluorophores are formed during the course of the fluorescent histochemical technique of Falck-Hillarp. The presumed catecholamine nature of the neuronal fluorogenic compound was investigated by microspectrofluorometry, and the spectral characteristics of the fluorescence in the taxonomically different species was found to be very similar (excitation maximum at 375 nm with a smaller peak or shoulder at 330 nm and sometimes a shoulder in the spectrum at 410 nm; emission maximum at 475 nm). The emission maximum coincides with that of the catecholamines and DOPA (475 nm). The excitation maximum (375 nm) directly after formaldehyde treatment, however, differs from that of the catecholamines and DOPA (410 nm), but is similar to the excitation maximum displayed by these catechol derivatives at acid pH. The spectral characteristics of the fluorophore in the sensory cells might therefore theoretically be explained by an acid pH in the cells. This seems improbable, however, and it is suggested that the phenomenon is due to the presence of unknown catechol derivatives. Analyses of the pH-dependent spectral changes indicate that the presumed catechol derivative in Tealia felina is -hydroxylated, whereas that in Anemia salina is not.     

Pulses of ammonia and methylamine induce down-regulation of nematocyte and nerve cell populations in Hydrozoa (Hydra; Hydractinia)

Summary Hydrozoa replace used-up nematocytes (cnidocytes) by proliferation and differentiation from interstitial stem cells (i cells). Repeated pulsed exposure ofHydra to elevated levels of unprotonated ammonia leads to successive loss of the various types of nematocytes: first of the stenoteles, then of the isorhizas and finally of the desmonemes. The loss is due to deficits in supply; the number of nematoblasts and differentiating intermediates is reduced. In the hydroidHydractinia the main process leading to numerical reduction was observed in vivo: mature nematocytes as well as precursors emigrate from their place of origin into the gastrovascular channels where they are removed by phagocytosis. This is a regular means by which these animals down-regulate an induced surplus of nematocytes. With lower effectiveness, pulses of methylamine, trimethylamine and glutamine also induce elimination of the nematocyte lineages. In the long term the population of nerve cells, which are permanently but slowly renewed from interstitial neuroblasts, decreases, too. After 2 months of daily repeated treatment the density of the Arg-Phe-amide-positive nerve cells was reduced to 50% of its normal level. Thus, ammonia induces down-regulation of all interstitial cell lineages. The temporal sequence of the ammonia-induced loss reflects the diverse rates with which the various i cell descendants normally are renewed.