Is the remodeling of the polyp prepattern in a hydrozoan planula a function of larval age or size and is it of “adaptive” significance?

Eggs of medusae develop into lecithotrophic planulae that undergo metamorphosis at different ages to form polyps. As planulae age they decrease in size as their yolk stores are utilized. The planulae of most Phialidium medusae develop into polyps where there is a decrease in the size of the holdfast region and a relative increase in the size of the hydranth region as they age. These changes occur independently of the decrease in planula size. In planulae with a decrease in the size of the holdfast region and an increase in the size of the hydranth-forming region there was a 50% decline in polyps that successfully stayed attached to the substrate after metamorphosis. These aged planulae produced an initial hydranth with the same number of tentacles as polyps from full-sized young planulae while young half-sized planulae produced hydranths where the tentacle number was smaller. The first phase of polyp colony growth with a small initial hydranth was slower than growth of a colony with a larger initial hydranth. Predation during this period led to more death in colonies with a small initial hydranth. The decline in successful attachment in aged planulae was not offset by the higher rate of growth and a smaller window of time where predation leads to death, suggesting that this age-related developmental change in planulae was not adaptive.     

Embryonic development and metamorphosis of the scyphozoan <Emphasis Type="Italic">Aurelia</Emphasis>

We investigated the development of Aurelia (Cnidaria, Scyphozoa) during embryogenesis and metamorphosis into a polyp, using antibody markers combined with confocal and transmission electron microscopy. Early embryos form actively proliferating coeloblastulae. Invagination is observed during gastrulation. In the planula, (1) the ectoderm is pseudostratified with densely packed nuclei arranged in a superficial and a deep stratum, (2) the aboral pole consists of elongated ectodermal cells with basally located nuclei forming an apical organ, which is previously only known from anthozoan planulae, (3) endodermal cells are large and highly vacuolated, and (4) FMRFamide-immunoreactive nerve cells are found exclusively in the ectoderm of the aboral region. During metamorphosis into a polyp, cells in the planula endoderm, but not in the ectoderm, become strongly caspase 3 immunoreactive, suggesting that the planula endoderm, in part or in its entirety, undergoes apoptosis during metamorphosis. The polyp endoderm seems to be derived from the planula ectoderm in Aurelia, implicating the occurrence of “secondary” gastrulation during early metamorphosis.     

Pattern of cell proliferation in embryogenesis and planula development ofHydractinia echinata predicts the postmetamorphic body pattern

Summary During embryogenesis and planula development of the colonial hydroidHydractinia echinata cell proliferation decreases in a distinct spatio-temporal pattern. Arrest in S-phase activity appears first in cells localized at the posterior and then subsequently at the anterior pole of the elongating embryo. These areas do not resume S-phase activity, even during the metamorphosis of the planula larva into the primary polyp. Tissue containing the quiescent cells gives rise to the terminal structures of the polyp. The posterior area of the larva becomes the hypostome and tentacles, while the anterior part of the larva develops into the basal plate and stolon tips. In mature planulae only a very few cells continue to proliferate. These cells are found in the middle part of the larva. Labelling experiments indicate that the prospective material of the postmetamorphic tentacles and stolon tips originates from cells which have exited from the cell cycle in embryogenesis or early in planula development. Precursor cells of the nematocytes which appear in the tentacles of the polyp following metamorphosis appear to have ceased cycling before the 38th hour of embryonic development. The vast majority of the cells that constitute the stolon tips of the primary polyp leave the cell cycle not later than 58 h after the beginning of development. We also report the identification of a cell type which differentiates in the polyp without passing through a post-metamorphic S-phase. The cell type appears to be neural in origin, based upon the identification of a neuropeptide of the FMRFamide type.     

Post-embryonic larval development and metamorphosis of the hydroidEudendrium racemosum (Cavolini) (Hydrozoa,Cnidaria)

The morphology and histology of the planula larva ofEudendrium racemosum (Cavolini) and its metamorphosis into the primary polyp are described from light microscopic observations. The planula hatches as a differentiated gastrula. During the lecithotrophic larval period, large ectodermal mucous cells, embedded between epitheliomuscular cells, secrete a sticky slime. Two granulated cell types occur in the ectoderm that are interpreted as secretory and sensorynervous cells, but might also be representatives of only one cell type with a multiple function. The entoderm consists of yolk-storing gastrodermal cells, digestive gland cells, interstitial cells, cnidoblasts, and premature cnidocytes. The larva starts metamorphosis by affixing its blunt aboral pole to a substratum. While the planula flattens down, the mucous cells penetrate the mesolamella and migrate through the entoderm into the gastral cavity where they are lysed. Subsequently, interstitial cells, cnidoblasts, and premature cnidocytes migrate in the opposite direction, i.e. from entoderm to ectoderm. Then, the polypoid body organization, comprising head (hydranth), stem and foot, all covered by peridermal secretion, becomes recognisable. An oral constriction divides the hypostomal portion of the gastral cavity from the stomachic portion. Within the hypostomal entoderm, cells containing secretory granules differentiate. Following growth and the multiplication of tentacles, the head periderm disappears. A ring of gland cells differentiates at the hydranth's base. The positioning of cnidae in the tentacle ectoderm, penetration of the mouth opening and the multiplication of digestive gland cells enable the polyp to change from lecithotrophic to planktotrophic nutrition.     

Endogenous photoproteins,calcium channels and calcium transients during metamorphosis in hydrozoans

Summary There are species of hydrozoans, Eutonina victoria, Mitrocomella polydiademata, and Phialidium gregarium whose eggs contain calcium-specific photoproteins. These cytoplasmic photoproteins are synthesized during oogenesis. During the cleavage stages of embryogenesis they are distributed to all of the cells of the developing planula larva. The amount of photoprotein slowly declines during the development of the planula larva, and markedly declines when the planula undergoes metamorphosis to become a polyp.Oocytes, unfertilized eggs, and fertilized eggs prior to the first cleavage do not produce light when treated with KCl. The ability to respond to KCl appears about the time of first cleavage, and is correlated with the appearance of active membrane responses. Both the KCl response and the action potentials will occur in sodium-free sea water, and both are inhibited by calcium channel blockers. These and other experiments suggest that voltage sensitive calcium channels first become active at about the time of first cleavage. These channels also appear on the same schedule in both unfertilized eggs and in enucleated egg fragments, which have been artificially activated with A23187.Developing planulae produce few or no spontaneous light responses before gastrulation. Later the frequency and magnitude of spontaneous light production increases presumably due to an increasing frequency and magnitude of calcium transients. Both the natural trigger of metamorphosis (bacteria) and an artificial trigger (CsCl) cause a conspicuous series of calcium transients. When these transients are inhibited by calcium channel blockers, metamorphosis is also inhibited.     

The Embryonic Origin of Neurosensory Cells and the Role of Nerve Cells in Metamorphosis in Phialidium gregarium (Cnidaria,Hydrozoa)

Summary

The embryonic origin of the nervous system in Phialidium gregarium was investigated. Entoderm-free planulae, surgically produced by bisection at mid-gastrulation, and normal planulae were examined by light and electron microscopy to determine their cellular composition. The cell types that occur in the epidermis of the normal planula were described. The entoderm-free planulae were found to be devoid of interstitial cells and their derivatives, the nematocytes and ganglion cells. Neurosensory cells were present, however, indicating that they are derivatives of the ectodermal epithelium.

The role of nerve elements in the initiation of metamorphosis was also examined. Normal and entoderm-free planulae treated for four hours with 0.4% colchicine at two, three, or four days of development fail to undergo cesium-induced metamorphosis. Since such treatment in other hydrozoans eliminates interstitial cells and their derivatives [1-3], it might be argued that ganglion cells are necessary to initiate metamorphosis. The observation that entoderm-free planulae, devoid of interstitial cell derivatives, are capable of responding to induction by bacteria or cesium, however, indicates that in Phialidium the colchicine effect is on other cell types. The results are compared with findings for other Cnidaria.     

Early development, pattern, and reorganization of the planula nervous system in Aurelia (Cnidaria, Scyphozoa)

We examined the development of the nervous system in Aurelia (Cnidaria, Scyphozoa) from the early planula to the polyp stage using confocal and transmission electron microscopy. Fluorescently labeled anti-FMRFamide, antitaurine, and antityrosinated tubulin antibodies were used to visualize the nervous system. The first detectable FMRFamide-like immunoreactivity occurs in a narrow circumferential belt toward the anterior/aboral end of the ectoderm in the early planula. As the planula matures, the FMRFamide-immunoreactive cells send horizontal processes (i.e., neurites) basally along the longitudinal axis. Neurites extend both anteriorly/aborally and posteriorly/orally, but the preference is for anterior neurite extension, and neurites converge to form a plexus at the aboral/anterior end at the base of the ectoderm. In the mature planula, a subset of cells in the apical organ at the anterior/aboral pole begins to show FMRFamide-like and taurine-like immunoreactivity, suggesting a sensory function of the apical organ. During metamorphosis, FMRFamide-like immunoreactivity diminishes in the ectoderm but begins to occur in the degenerating primary endoderm, indicating that degenerating FMRFamide-immunoreactive neurons are taken up by the primary endoderm. FMRFamide-like expression reappears in the ectoderm of the oral disc and the tentacle anlagen of the growing polyp, indicating metamorphosis-associated restructuring of the nervous system. These observations are discussed in the context of metazoan nervous system evolution.     

海蜇胚胎发育和变态过程超微观察

采用扫描电镜、透射电镜和蛋白银染色等方法研究了海蜇胚胎发育和变态过程中细胞超微结构变化。结果显示: (1)海蜇自受精卵至原肠期阶段细胞均等分裂, 细胞间存在大量连接, 细胞形态相近, 未出现显著分化; (2)海蜇自早期浮浪游虫阶段, 其外胚层细胞开始出现空泡化, 至4触手螅状体阶段外胚层细胞空泡体积逐渐增大, 而内胚层细胞仅在4触手螅状体阶段才出现空泡化。伴随着外胚层细胞空泡化比例的增大, 杯状体和4触手螅状体阶段出现疑似凋亡小体结构; (3)刺细胞分化于早期浮浪游虫期的外胚层近中胶层区域, 而后逐渐向外转移, 至4触手螅状体阶段发育成熟并转移至表面; (4)纤毛形成于早期浮浪幼虫, 在杯状体阶段逐渐退化, 并于4触手螅状体阶段完全消失; (5)在海蜇早期发育各个阶段, 其内部均发现大量着色较深的卵黄体, 且在浮浪游虫阶段首次发现了海蜇外层细胞主动吞噬细菌现象, 表明海蜇早期发育营养来自内源性和外源性两部分。研究结果可为阐明刺胞动物早期发育模式提供依据。     

Relay-ray way of hydroplasm movement in hydroid colonies

In this study, we continued the investigation of the distribution system of colonial hydroids in the course of its development, starting with its emergence during the planula metamorphosis and ending with the formed colony. The hydroplasmic stream system of two species of colonial hydroids—Perigonimus abyssi G.O. Sars, 1874, and Stauridia producta Wright, 1858—was studied. We found that the main principle by which hydroplasma moves in these colonies, which form no shoots, is the relay-race from one hydranth to another through a stolon fragment connecting them or it moves past the neighbouring hydranth to the next one, etc. We show that the efficiency of the conducting (distribution) system does not depend on the level of complexity of the colonial structure. The results of this study confirm the absence of general colonial processes of integration and self-regulation in hydroid polyps.     

On some features of embryonic development and metamorphosis of Aurelia aurita (Cnidaria, Scyphozoa)

Aurelia aurita is a cosmopolite species of scyphomedusae. Its anatomy and life cycle are well investigated. This work provides a detailed study on development and structure of A. aurita planula before and during its metamorphosis. Intravital observations and histology study during the settlement and metamorphosis of the planulae demonstrated that the inner manubrium lining of primary polyp (gastroderm) develops from the ectoderm of the planula posterior end. The spatial and temporal dynamics of serotonergic cells from the early embryonic stages until the formation of the primary polyp were studied for the first time. In addition, the distribution of tyrosinated tubulin and neuropeptide RF-amide at different stages of A. aurita development was traced.     

Metamorphosis ofHydractinia echinata Insights into pattern formation in Hydroids

Summary Hydractinia echinata is a marine, colony-forming coelenterate. Fertilized eggs develop into freely swimming planula larvae, which undergo metamorphosis to a sessile (primary) polyp. Metamorphosis can be triggered by means of certain marine bacteria and by Cs⁺. Half a day after this treatment a larva will have developed into a polyp. The induction of metamorphosis can be prevented by addition of inhibitor I, a substance partially purified from tissue ofHydra. The larvae ofH. echinata also appear to contain this substance. Inhibitor I appliedafter the onset of metamorphosis blocks its continuation as long as it remains in the culture medium. Cs⁺ applied within the same period of time also blocks the continuation of metamorphosis. However, these two agents have opposite effects on the body pattern of the resultant polyps. The experiments indicate that application of Cs⁺ triggers the generation of the pre-pattern. Inhibitor I appears to be a factor of this prepattern. A model is proposed which describes the basic features of head and foot/stolon formation not only forHydractinia but also for other related hydroids.     

A cnidarian neuropeptide of the GLWamide family induces metamorphosis of reef-building corals in the genus <Emphasis Type="Italic">Acropora</Emphasis>

Coral larvae appear to sense appropriate environments for settlement and start metamorphosis by converting external cues into internal signals, although little is known about these molecular mechanisms. A family of neuropeptides, GLWamides, are thought to be such internal signals, acting hormonally to induce metamorphosis in some hydrozoan species. Here we report that one member of the GLWamide peptide family, Hym-248, can induce metamorphosis of planula larvae in the genus Acropora. The Acropora planulae responded to the peptide in a concentration-dependent manner. The GLWamide peptide would mimic endogenous molecules to start metamorphosis in Acropora as in case of hydrozoans. In addition, the peptide could be applied to produce "coral seedlings" with the aim of reef restoration.     

Comparative fine structural studies of planulae and primary polyps of identical age of the sea pen,Ptilosarcus gurneyl

Electron microscopic study of an 18-day-old planulae and primary polyps of the sea pen, Ptilosarcus gurneyi, reveals 14 cell types: sustentacular cell A, sustentacular cell B, nerve cell, sensory cell, cnidoblast, interstitial cell, five types of gland cell (A, B, C, D and E), amoebocyte, style cell and endodermal cell. Of these, 9 are found in the planula, 12 in polyps and 7 are common to both stages. The fine structure of all cell types is described. Since the planulae and polyps in this study were identical in age of development, the gaining and losing of certain types of cells in the polyp are attributed to changes associated with settlement and metamorphosis. Modifications of the seven common cell types during metamorphosis can also be attributed to the change of life style from pelagic to benthic.     

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

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

On the Morphology of Actiniarian Larvae

Planktonic larvae of the Athenaria correspond in a number of morphological characteristics to plankto-trophic thenarian planulae. In edwardsiid planulae there are often, during the later part of the planktonic phase, a well-developed aboral physa-"Anlage" and six triangular tentacles. Holotrichous haplonemes are not uncommon in actiniarian planulae. This nemato-cyst type is, however, limited to the larva stage in the edwardsiid and some thenarian species. The phylogenetical connection between the edwardsiid and the planktotrophic thenarian planulae is stressed The striking morphological resemblances between madreporarian and lecithotrophic planulae of the family Actiniidae indicate a close phylogenetic connection between the two planula types.     

Cellular and intracellular pathways mediating the metamorphic stimulus in hydrozoan planulae

Summary Both the natural metamorphic stimulus (an unidentified bacterial product) and an artificial trigger of metamorphosis (Cs⁺) cause large calcium transients in planula cells of the hydrozoanMitrocomella polydiademata. When these transients are inhibited with calcium channel blockers, metamorphosis is also inhibited. All cells of theMitrocomella planula contain a calcium-specific photoprotein. The cells where the calcium transients occur during natural- and Cs⁺-induced metamorphosis have been visualized in normal and entoderm free planulae that lack ganglion cells, using a compound microscope coupled to an image intensifier and video camera. During bacteria- and Cs⁺-induced metamorphosis, groups of contiguous cells, occupying from about 10% to the entire visible surface of the planula, simultaneously exhibit calcium transients. When the cells that initiate a transient comprise only part of the planula surface, the calcium transient frequently propagates and can eventually involve every cell on the visible planula surface. There is no special site on the planula surface where calcium transients are more apt to be initiated. There is no indication that propagation of a flash in one direction is more likely than in another. The velocity of propagation is virtually the same in all directions. The only feature of the spatial distribution of bacteria- and Cs⁺-induced calcium transients that appears to be necessary for the induction of metamorphosis is that at least one transient must involve all of the surface cells of the planula. The spatial behavior of calcium transients is the same in entoderm free planulae (lacking ganglion cells) as in normal planulae. The propagation of these calcium transients most probably occurs via epithelial conduction. This metamorphic step involving calcium transients is probably the intercellular communication system that informs the cells of the planula that metamorphosis will commence.Metamorphosis inMitrocomella planulae can also be induced with phorbol esters. Calcium transients do not occur during phorbol ester-induced metamorphosis, indicating that they act at a different point in the metamorphic pathway. Calcium channel blockers do not inhibit phorbol ester-induced metamorphosis. Inhibitors of protein kinase-C, inhibit both phorbol ester-induced metamorphosis and Cs⁺- and bacteria-induced metamorphosis, but have no effect on the calcium transients induced by Cs⁺. This indicates that the calcium transient mediated step in the metamorphic pathway occurs prior to protein kinase-C activation. Calcium transients probably play a major role in activating protein kinase-C.     

The biology of coral metamorphosis: molecular responses of larvae to inducers of settlement and metamorphosis

Like many other cnidarians, corals undergo metamorphosis from a motile planula larva to a sedentary polyp. In some sea anemones such as Nematostella this process is a smooth transition requiring no extrinsic stimuli, but in many corals it is more complex and is cue-driven. To better understand the molecular events underlying coral metamorphosis, competent larvae were treated with either a natural inducer of settlement (crustose coralline algae chips/extract) or LWamide, which bypasses the settlement phase and drives larvae directly into metamorphosis. Microarrays featuring > 8000 Acropora unigenes were used to follow gene expression changes during the 12 h period after these treatments, and the expression patterns of specific genes, selected on the basis of the array experiments, were investigated by in situ hybridization. Three patterns of expression were common—an aboral pattern restricted to the searching/settlement phase, a second phase of aboral expression corresponding to the beginning of the development of the calicoblastic ectoderm and continuing after metamorphosis, and a later orally-restricted pattern.     

Inductive activity of the posterior tip of planula in the marine hydroid Dynamena pumila

Activity of organizer regions is required for body plan formation in the developing organism. Transplanting a fragment of such a region to a host organism leads to the formation of a secondary body axis that consists of both the donor's and the host's tissues (Gerhart, 2001). The subject of this study, the White Sea hydroid cnidarian Dynamena pumila L. (Thecaphora, Sertulariidae), forms morphologically advanced colonies in the course of complex metamorphosis of the planula larva. To reveal an organizer region, a series of experiments has been performed in which small fragments of donor planula tissues were transplanted to embryos at the early and late gastrula stage, as well as to planulae. Only transplantations of a posterior tip fragment of a donor planula to a host planula of the same age led, in the course of metamorphosis, to the formation of a secondary shoot, which involved up to 50% of the host's tissues. After transplantations of tissue fragments of the anterior tip and the middle of the planula body, the formation of any ectopic structures was never observed. It was concluded that the posterior tip of the planula has organizer properties in Dynamena.     

The cleavage initiation site establishes the posterior pole of the hydrozoan embryo

Summary When the first cleavage of the hydrozoan egg is reversibly suppressed, two cleavage furrows frequently form simultaneously at the time of the second cleavage. If these two cleavage initiation sites are far enough apart, each one specifies a site of gastrulation, and the embryo that forms develops into a two tailed planula larva. When two tailed planulae are induced to metamorphose, they form a polyp with two stalks and hydranths.