Histological and ultrastructural studies of the basal disk of Hydra

Summary The gastrodermis and mesoglea of the basal disk of Hydra were investigated to conclude a three-part series of papers. The gastrodermis is composed of digestive cells (most predominant cell type), mucous and nerve cells (both immature and fully differentiated). The principal function of the digestive cells appears to be storage of protein, lipid and glycogen reserves which are utilized by neighboring cells. Mucous cells apparently use some of the reserves to synthesize their secretions which lubricate cells and prevent cell damage during egestion of waste through the aboral pore. The function of the gastrodermal nerve cells is uncertain.The mesoglea of the basal disk, contains the same structural components as seen in other regions of the polyp. It is reasonable to assume that it maintains the same function of cell adhesion and migration. As the mesoglea converges on the aboral pore, it loses its structural integrity and cells are sloughed off the column.This investigation was supported by The National Science Foundation, Grant Number GB-27395.     

Isolation of tissue layers in hermatypic corals by N-acetylcysteine: morphological and proteomic examinations

Corals are diploblastic in body pattern and include two tissue layers, the epidermis and gastrodermis, interconnected by an acellular matrix mesoglea. During development, cells in these tissue layers differentiate morphologically and functionally. In most hermatypic corals, the gastrodermis further develops an ability to associate with microalgae dinoflagellates. This endosymbiosis occurs inside specific host gastrodermal cells, and its mechanism still remains unclear notwithstanding decades of research. The delay in progress is partly due to the difficulty in separating the gastrodermis and its symbionts from the epidermis for detailed cellular and biochemical investigations. The present study reports a simple method to separate these two tissue layers in hermatypic corals using the reducing agent, N-acetylcysteine (NAC). Efficient tissue and proteomic isolations are demonstrated by microscopy and two-dimensional SDS polyacrylamide gel electrophoresis (2D SDS-PAGE). The NAC treatment was able to separate tissue layers without inducing protein degradation. Furthermore, the sensitivity of protein detection greatly increases in the isolated tissue layers. The application of the present technique provides future research on endosymbiosis and coral development with a tool for higher accuracy and sensitivity.     

Cellular differentiation and morphogenesis in Cordylophora

Summary The interstitial cells ofCordylophora were destroyed by treating animals with 4,500 Roentgens of x-irradiation. Within 5–6 days after treatment no interstitial cells were detected in the treated animals and they were never seen in later stages. Some cell divisions were noted in the epidermal epithelio-muscular cells of the x-rayed animals which survived for four weeks. This was ample time to perform reaggregation-reconstitution experiments.Isolated, untreated coenosarc formed a mass from which hydranths and stolons arose. X-rayed coenosarc also formed these structures, although regenerative capacity was less than that of normal coenosarc. The number of stolons and hydranths produced decreased with length of time after irradiation. Both normal and x-rayed coenosarc masses exhibited a tendency to form a greater number of hydranths than stolons when the ratio of epidermis to gastrodermis was low and a greater number of stolons when the ratio of epidermis to gastrodermis was high. Masses prepared from the amounts of epidermis and gastrodermis normally found in intact animals produced intermediate numbers of hydranths and stolons.Isolated, untreated epidermis produced a gastrodermal layer from interstitial cells. They migrated to the inner surface of the epidermal epithelio-muscular cells, enlarged and differentiated into typical gastrodermal-digestive cells. These preparations formed hydranths and developed into colonies. X-irradiated epidermis did not form an inner gastrodermal layer but did secrete perisarc on the periphery. In some ases a second layer of epidermal epithelio-muscular cells was noted on the interior of the x-rayed masses. However, none of the irradiated epidermal masses produced hydranths or stolons or survived to form colonies.Gastrodermis was isolated from normal animals and although the cells rounded up into a spherical mass no morphogenesis occurred and the masses disintegrated within 12–24 hours. Irradiated gastrodermis behaved in the same manner.Normal epidermis was applied to x-rayed gastrodermis and from these preparations normal animals were produced.Normal, untreated gastrodermis combined with x-rayed epidermis yielded viable animals. Interstitial cells appeared to be produced by dedifferentiation of gland cells. The interstitial cells thus formed were able to divide and differentiate into cnidoblasts typical of epidermis.Thus, inCordylophora both epidermal and gastrodermal cells have the capacity to form cell types characteristic of the reciprocal layer.

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Zusammenfassung Die Interstitialzellen vonCordylophora wurden durch Röntgenbestrahlung (4,500 r) zerstört. 5–6 Tage nach der Bestrahlung waren keine Interstitialzellen mehr feststellbar, und auch in späteren Stadien traten nie mehr solche auf. Einige Zellteilungen wurden in den Epithel-Muskelzellen der bestrahlten Tiere beobachtet. Die Tiere blieben 4 Wochen am Leben, so daß Reaggregations- und Rekonstitutionsexperimente durchgeführt werden konnten.Isoliertes, unbehandeltes Coenosark bildete eine Zellmasse, aus der heraus Hydranthen und Stolonen wuchsen. Dieselben Strukturen entstanden aus bestrahltem Coenosark, wenn auch die Regenerationsfähigkeit des bestrahlten Cornosarks vermindert war. Die Zahl der gebildeten Hydranthen und Stolonen nahm mit zunehmender Zeit nach der Bestrahlung ab. Normale und auch bestrahlte Coenosark-Massen bildeten im allgemeinen mehr Hydranthen als Stolonen, wenn das Verhältnis Epidermis: Gastrodermis niedrig war, aber mehr Stolonen, wenn dag Verhältnis hoch war. Coenosark-Massen, die Epidermis und Gastrodermis im normalerweise vorhandenen Verhältnis enthielten, bildeten intermediäre Zahlen von Hydranten und Stolonen aus.Isolierte, unbehandelte Epidermis bildete aus Interstitialzellen eine Gastrodermisschicht. Dabei wanderten die Interstitialzellen auf die innere Oberfläche der epidermalen Epithelmuskelzellen, wurden größer, und bildeten typische gastrodermale Verdauungszellen. Solche Präparate bildeten Hydranthen und entwickelten sich in Kolonien. Bestrahlte Epidermis bildete keine Gastrodermis aus, sezernierte aber Perisark auf der Peripherie. In einigen Fällen wurde eine zweite Schicht von epidermalen Epithelmuskelzellen beobachtet im Innern der bestrahlten Massen. Me aber bildete eine bestrahlte Epidermismasse Hydranthen oder Stolonen, und nie Kolonien.Wenn Gastrodermis aus normalen Tieren isoliert wurde, rundeten sich die Zellen sich zu einer kugeligen Masse ab, aber es kam nie zu einer Morphogenese, und die Massen desintegrierten innerhalb 12–24 Std. Bestrahlte Gastrodermis verhielt sich ebenso.Wenn normale Epidermis auf bestrahlte Gastrodermis gepflanzt wurde, entstanden normale Tiere.Wenn normale Gastrodermis mit bestrahlter Epidermis kombiniert wurde, entstanden ebenfalls normale Tiere. Interstitialzellen entstanden durch Dedifferenzierung von Drüsenzellen. Die dabei gebildeten Interstitialzellen teilten sich und bildeten für Epidermis typische Cnidoblasten. Bei Cordylophora haben demzufolge epidermale, als auch gastrodermale Zellen die Fähigkeit, Zellen der reziproken Zellschicht auszubilden.

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The author wishes to acknowledge the financial aid received for this project from the National Institutes of Health, Bethesda, Md. through their University Biomedical Sciences Support Program.     

Ultrastructural features of the trophonema and oogenesis in the starlet sea anemone, Nematostella vectensis (Edwardsiidae)

Abstract. The starlet sea anemone, Nematostella vectensis Stephenson 1935, is a burrowing, estuarine species that has become a model organism for fundamental studies of cnidarian and metazoan development. During early oogenesis, oocytes appear in the basal region of the gastrodermis in the reproductive mesenteries and gradually bulge into the adjacent connective tissue space (mesoglea) where the majority of oocyte growth and vitellogenesis occurs. However, oocytes do not physically contact the cellular and amorphous matrix of the mesogleal compartment due to a thin, intervening basal lamina. Oocytes retain limited contact with the basal gastrodermal epithelium via groups of ultrastructurally modified gastrodermal cells called trophocytes. Trophocytes are monociliated accessory cells of somatic origin that collectively form a structure called the trophonema, a unique accessory cell/oocyte association not observed outside the Cnidaria. The trophonema consists of 50–60 trophocytes that maintain contact with <1% of the oocyte surface and forms a circular, bowel‐shaped depression on the luminal surface of the gastrodermis as they sink into the mesoglea with the oocyte. The oocyte remains highly polarized throughout oogenesis with the germinal vesicle positioned near the trophonema and presumably representing the future animal pole of the embryo. Contact between the trophonema and the oocyte is restricted to cell junctions connecting peripheral trophocytes and narrow extensions from the oocyte. Previous studies suggest that the trophonema plays a role in transport of extracellular digestive products from the gastrovascular cavity to the oocyte, and the ultrastructural features described in this study are consistent with that view. Vitellogenesis is described for the first time in a sea anemone. Yolk synthesis involves both autosynthetic and heterosynthetic processes including the biosynthetic activity of the Golgi complex and the uptake of extraoocytic yolk precursors via endocytosis, respectively.     

Immunogold-labeled S-phase neoblasts, total neoblast number, their distribution, and evidence for arrested neoblasts in Macrostomum lignano (Platyhelminthes, Rhabditophora)

Neoblasts in Platyhelminthes are the only cells to proliferate and differentiate into all cell types. In Macrostomum lignano, the incorporation of 5'-bromo-2'-deoxyuridine (BrdU) in neoblasts confirmed the distribution of S-phase cells in two lateral bands. BrdU labeling for light and for transmission electron microscopy (TEM) identified three populations of proliferating cells: somatic neoblasts located between the epidermis and gastrodermis (mesodermal neoblasts), neoblasts located within the gastrodermis (gastrodermal neoblasts), and gonadal S-phase cells. In adults, three stages of mesodermal neoblasts (2, 2-3, and 3) defined by their ultrastructure were found. Stage 1 neoblasts where only seen in hatchlings. These stages either were phases within the S-phase of one neoblast pool or were subsequent stages of differentiating neoblasts, each with its own cell cycle. Regular TEM and immunogold labeling provided the basis for calculating the total number of neoblasts and the ratio of labeled to non-labeled neoblasts. Somatic neoblasts represented 6.5% of the total number of cells. Of these, 27% were labeled in S-phase. Of this fraction, 33% were in stage 2, 46% in stage 2-3, and 21% in stage 3. Immunogold labeling substantiated results concerning the differentiation of neoblasts into somatic cells. Non-labeled stage 2 neoblasts were present, even after a 2-week BrdU exposure. Double labeling of mitoses and FMRF-amide revealed a close spatial relationship of mesodermal neoblasts with the nervous system. Immunogold-labeled sections showed that nearly 70% of S-phase cells were in direct contact or within 5 microm from nerve cords.     

Ultrastructural evidence for the presence of nerve cells in the gastrodermis of Hydra

Summary Two types of nerve cells, namely, neurosensory and neurosecretory cells have been identified and described in the gastrodermis of Hydra pseudoligactis. The morphological criteria used for the identification of gastrodermal nerves are based on those presented previously for epidermal nerves. The third type of nerve cell in the epidermis, ganglionic cells, was not observed in these studies. The distribution, function and origin of gastrodermal nerve cells are discussed briefly.With the technical assistance of Linda M. Bookman.     

Metamorphosis and acquisition of symbiotic algae in planula larvae and primary polyps of Acropora spp.

Coral planulae settle, then metamorphose and form polyps. This study examined the morphological process of metamorphosis from planulae into primary polyps in the scleractinian corals Acropora nobilis and Acropora microphthalma, using the cnidarian neuropeptide Hym-248. These two species release eggs that do not contain Symbiodinium. The mode of acquisition of freshly isolated Symbiodinium (zooxanthellae) (FIZ) by the non-symbiotic polyp was also examined. Non-Hym-248 treated swimming Acropora planulae did not develop blastopore, mesenteries or coelenteron until the induction of metamorphosis 16 days after fertilization. The oral pore was formed by invagination of the epidermal layer after formation of the coelenteron in metamorphosing polyps. At 3 days after settlement and metamorphosis, primary polyps exposed to FIZ established symbioses with the Symbiodinium. Two–four days after exposure to FIZ, the distribution of Symbiodinium was limited to the gastrodermis of the pharynx and basal part of the polyps. Eight–ten days after exposure to FIZ, Symbiodinium were present in gastrodermal cells throughout the polyps.     

Schistosoma mansoni: an in vivo study of drug-induced autophagy in the gastrodermis

The effects of Astiban, Lucanthone, Hycanthone and Niridazole on autophagic activities in the gastrodermis of Schistosoma mansoni were determined in vivo, using different dosage levels and dosage times. With Astiban, high levels of autophagy were observed in the gastrodermis 2 hours after an injection of the drug into the mouse, and this response had declined by 20 hours, marking a recovery by the parasite from the drug. Hycanthone and Lucanthone produced an autophagic response several days after the onset of treatment, and no recovery was observed in the morphology of the gastrodermis after the drug was discontinued. The effects of Niridazole on the gastrodermis were to produce the most dramatic ultrastructural changes after high doses and over several days of treatment. With all the drugs examined, gastrodermal autophagy was characterized by the formation of vacuoles containing cell components, lipid droplets and sometimes hydrolytic enzyme reaction product. The autophagic vacuoles appeared to be formed by the sequestration of cytoplasmic material by the basal membrane infoldings, and the transfer of enzymes into the vacuole from within the limiting membrane. The residues from intracellular digestion appeared to be emptied into the caecal lumen.     

Ultrastructure of neurons and synapses in the tentacle gastrodermis of the sea anemone Calliactis parasitica

Little is known about gastrodermal neurons and synapses in the tentacles of sea anemones. Using transmission electron microscopy of serial thin sections of Calliactis parasitica, we have identified both a sensory cell and a ganglion cell with granular vesicles originating from the Golgi complex and have identified four types of synapses in the tentacular gastrodermal nerve plexus. The sensory cell has a recessed apical cilium with a basal body and a perpendicularly oriented centriole, below which are several strands of striated rootlets surrounded by mitochondria. The ganglion cell lacks a cilium and resembles a bipolar neuron, with oppositely directed processes lying parallel to the basally located circular smooth muscle. Both one-way and two-way interneuronal synapses are present with 60- to 90-nm granular vesicles of various densities aligned at the paired electron-dense membranes and fine cross filaments in the intervening 13-nm cleft. Two types of neuroeffector synapses have been located. Dense granular vesicles are present at neuromuscular synapses, whereas less dense vesicles are present at neuroglandular synapses. Most of the synaptic vesicles range from 60 to 120 nm in diameter. Two types of nerve cells and a variety of synaptic loci provide morphological substrates for the spontaneous SS2 conduction pulses in the tentacular gastrodermis of C. parasitica. J Morphol 231:217–223, 1997. © 1997 Wiley-Liss, Inc.     

Quantitative analysis of cell types during growth,degrowth and regeneration in the planarians Dugesia mediterranea and Dugesia tigrina

A method of tissue maceration (dissociation) of planarian tissues into single cells was used to characterize the basic cell types in the planarians Dugesia mediterranea and Dugesia tigrina, and to determine the total cell number and distribution of cell types during growth, degrowth and regeneration.Using this method, 13 basic cell types have been determined for both species. The total number of cells increases with body length and volume whereas the distribution of cell types is only slightly affected. Growth and degrowth occur mainly through changes in total cell number leaving cell distribution only moderately affected. During regeneration, an increase in neoblast density in the blastema followed later on by increases in nerve cells are the more significant changes detected.These results are discussed in relation to mechanisms of cell renewal, blastema formation and maintenance of tissue polarity.Abbreviations nb neoblasts - nv nerve cells - ep epidermal cells - fp fixed parenchyma cells - g gastrodermal cells     

Ratiometric imaging of gastrodermal lipid bodies in coral–dinoflagellate endosymbiosis

Cnidaria–dinoflagellate endosymbiosis is the phenomenon of autotrophic symbionts living inside the gastrodermal cells of their animal hosts. The molecular mechanism that regulates this association remains unclear. Using quantitative microscopy, we now provide evidence that the dynamic lipid changes in gastrodermal “lipid bodies” (LBs) reflect the symbiotic status of the host cell and its symbiont in the hermatypic coral Euphyllia glabrescens. By dual-emission ratiometric imaging with a solvatochromic fluorescent probe, Nile red (9-diethylamino-5H-benzo[α]phenoxazine-5-one), we showed that the in situ distribution of polar versus neutral lipids in LBs in living gastrodermal cells and symbionts can be analyzed. The ratio of Nile red fluorescence at red (R) versus green (G) wavelength region (i.e., R/G ratio) correlated with the relative molar ratio of polar (P) versus neutral (NP) lipids (i.e., P/NP ratio). The R/G ratio in host LBs increased after bleaching, indicating a decrease in neutral lipid accumulation in gastrodermal cells. On the other hand, neutral lipid accumulation inside the symbiont LBs resulted in gradual decreases of the R/G ratio as a result of bleaching. In comparison with the bleaching event, there was no relative lipid concentration change in host LBs under continual light or dark treatments as shown by insignificant R/G ratio shift. Patterns of R/G ratio shift in symbiont LBs were also different between corals undergoing bleaching and continual light/dark treatment. In the latter, there was little lipid accumulation in symbionts, with no resulting R/G ratio decrease. These results, demonstrating that the symbiotic status positively correlated with morphological and compositional changes of lipid bodies, not only highlight the pivotal role of LBs, but also implicate an involvement of lipid trafficking in regulating the endosymbiosis.     

Cellular structure and ultrastructure of the black coral Antipathes aperta: 2. The gastrodermis and its collar cells

The gastrodermis of the black coral Antipathes aperta is associated with eight distinct types of cells, including two types of microbasic b-mastigophores (nematocysts), spumous and vesicular mucus cells, and ganglion cells that are essentially the same as in the epidermis. Three additional types of cells are unique to the gastrodermis, and are readily distinguished from those of the epidermis by their electron-opaque inclusions. These include lipoidal cells, zymogen digestive cells, and an unusual type of epitheliomuscular collar cell. The pharyngeal region is characterized by the presence of electron-opaque nematocysts, a scattering of zymogen cells, and a large number of collar cells. The latter are distinguished in part by the presence of dense microfibrillar processes that surround the microvilli and extend into adjacent collars. This interconnection results in the formation of an extensive pharyngeal meshwork. These collar cells are additionally distinguished by the placement of the collar and flagellum adjacent to a flared cup of cytoplasm. This portion of the cell is capable of endocytosis of relatively large unicellular prey, and apparently is capable of forming digestive vesicles as well. The pharyngeal gastrodermis grades into simple lobate septal filaments toward the base of the coelenteron, where large, granular nematocysts all but replace the smaller electron-opaque types Collar cells are found here as well, but in fewer numbers compared to the zymogen cells. Ultrastructural results are compared with those of other coelenterates and discussed in terms of food and modes of nutrition.     

The fine structure of the hypostome and mouth of hydra

Summary The normal morphology of the hypostome and mouth of hydra were examined by transmission electron microscopy with conventional thin sections and freeze-fracture replicas. Myonemes of the hypostome are small in diameter, have gap and intermediate-type cell junctions within each epithelial layer and are associated with the opposite epithelial layer by transmesogleal processes and gap junctions. Nematocysts and sensory cells are aggregated in the circumoral region. The fine structure of adherent flagella arising from gastrodermal gland cells, and the transition region at the mouth between epidermis and gastrodermis are described in detail for the first time. The possible functional significance of the findings is discussed.     

Studies on Stenostomum grande Child, 1902 (Platyhelminthes,Catenulida): fine structure of the digestive tract and the endocytotic activity of the gastrodermis

Abstract The digestive tract and its endocytotic activity in the catenulid Stenostomum grande were studied by electron microscopy. The pharynx was typical of the simplex type. At the mouth, between the integumental epithelium and the pharyngeal epithelium proper, was a transition zone. Among the epithelial cells of this transition were monociliated sensory cells and the necks of bucco-pharyngeal secretory cells of two types. The pharyngeal epithelium proper was densely ciliated, with long ciliary rootlets and mitochondria. It was surrounded by two layers of muscles. The gastrodermis consisted of phagocytes and typical secretory Minotian cells. It was underlain by a delicate basal lamina and muscle fibers. Distinctive of the phagocytes was the presence of differentiated cilia, cup-shaped mitochondria, and vacuoles with dense inclusions. Morphological differences between pharyngeal and gastrodermal cilia suggest functional differences. Experiments using latex beads as tracers and the identification of acid phosphatase in cytoplasmic vacuoles pointed to a high level of endocytotic and digestive activity in the phagocytes. Our data demonstrate that the basic structure of the digestive tract in S. grande conforms well to that of other free-living platyhelminths, but it does have ultrastructural peculiarities.     

Developmentally regulated localization of endosymbiotic dinoflagellates in different tissue layers of coral larvae

In adult cnidarians, symbiotic dinoflagellate Symbiodinium are usually located in the gastrodermis. However, the onset of this endosymbiotic association and its regulation during larval development are unclear. This study examined the distribution of the Symbiodinium population in tissue layers of planula larvae released from the stony coral Euphyllia glabrescens. Symbiodinium were redistributed from the epidermis to the gastrodermis, at a rate that was fastest during early planulation and then decreased prior to metamorphosis. This process indicates that the endosymbiotic activity of coral tissues is developmentally regulated. During the early larval stage, both the epidermis and gastrodermis contained Symbiodinium; then, as the larvae developed toward metamorphosis, the numbers in the epidermis gradually diminished until they were only found in the gastrodermis. The mechanism of redistribution remains unknown, but may be due to a direct translocation and/or change in the proliferation of symbionts in different tissue layers.     

Further observations on dividing and non-dividing cnidoblasts in the regenerating isolated gastrodermis of Hydra

Summary Cnidoblasts derived from the dedifferentiation of gland cells in the regenerating isolated gastrodermis of Hydra are capable of nuclear and cytoplasmic division. The daughter cell containing the nematocyst apparently develops normally. The fate of the other daughter cell remains obscure, but it is believed that it is also capable of developing a nematocyst. Only a single bi-nucleated cnidoblast was observed and it was in the process of degeneration. It is suggested that at least in the present system, cnidoblasts are derived not only from interstitial cells but also from pre-existing cnidoblasts.This investigation was supported by the National Science Foundation Grant No. GB 8384.With the technical assistance of Linda Bookman.     

Numbers, distribution, and types of neurons in the pedal disk of Hydra based on a serial reconstruction from transmission electron micrographs

The numbers, distribution, and types of neurons in a pedal disk of Hydra littoralis were determined from electron micrographs of 567 serial sections approximately 0.12 micron thick. Of 248 neurons counted, we found 234 ganglion cells in the epidermis and 14 in the gastrodermis. No sensory cells with surface projecting cilia were observed in either epithelial layer of the foot region. We found ciliary structures in 196 (84%) of the epidermal neurons: 55 had a well defined cilium-stereociliary complex, 30 had a cilium lacking stereocilia, and 111 could not be classified. In contrast, 38 epidermal neurons lacked evidence of ciliary structures; 10 of the 14 gastrodermal neurons had one or more centrioles, some with an elaborate pericentriolar rootlet system, but no cilium or stereocilia. Neuronal perikarya could be classified into those with dense heterochromatic nuclei and those with light granular nuclei; often these two nuclear variations were observed in paired or triad arrangements of epidermal neurons. In addition, 68 (29%) of the epidermal neurons were characterized by the presence of small dense granules (115-178 nm in diameter) in the cytoplasm around the periciliary space. Although 32 pairs and 5 triads of contiguous neuronal perikarya were present in the epidermis, only two paired neuronal perikarya were present in the gastrodermis. The major concentration of neurons was approximately midway between the basal surface and the region of transition of epitheliomuscular cells into glandulomuscular cells. There was no evidence of large neuronal aggregations suggestive of ganglia in the pedal disk.     

The embryonic development of the triclad <Emphasis Type="Italic">Schmidtea polychroa</Emphasis>

Triclad flatworms are well studied for their regenerative properties, yet little is known about their embryonic development. We here describe the embryonic development of the triclad Schmidtea polychroa, using histological and immunocytochemical analysis of whole-mount preparations and sections. During early cleavage (stage 1), yolk cells fuse and enclose the zygote into a syncytium. The zygote divides into blastomeres that dissociate and migrate into the syncytium. During stage 2, a subset of blastomeres differentiate into a transient embryonic epidermis that surrounds the yolk syncytium, and an embryonic pharynx. Other blastomeres divide as a scattered population of cells in the syncytium. During stage 3, the embryonic pharynx imbibes external yolk cells and a gastric cavity is formed in the center of the syncytium. The syncytial yolk and the blastomeres contained within it are compressed into a thin peripheral rind. From a location close to the embryonic pharynx, which defines the posterior pole, bilaterally symmetric ventral nerve cord pioneers extend forward. Stage 4 is characterized by massive proliferation of embryonic cells. Large yolk-filled cells lining the syncytium form the gastrodermis. During stage 5 the external syncytial yolk mantle is resorbed and the embryonic cells contained within differentiate into an irregular scaffold of muscle and nerve cells. Epidermal cells differentiate and replace the transient embryonic epidermis. Through stages 6–8, the embryo adopts its worm-like shape, and loosely scattered populations of differentiating cells consolidate into structurally defined organs. Our analysis reveals a picture of S. polychroa embryogenesis that resembles the morphogenetic events underlying regeneration.Edited by D. Tautz     

Histochemical and ultrastructural observations on feeding and digestion in Reighardia sternae (Pentastomida: Cephalobaenida)

Histological, histochemical and ultrastructural methods have been used to study gut structure and function in the cephalobaenid pentastomid Reighardia sternae (Diesing, 1864).
R. sternae feeds exclusively on blood. Haemolysis of ingested erythrocytes is thought to be initiated by non-specific esterase secreted by cells lining the posterior oesophagus. Only one other enzyme, acid phosphatase, was demonstrated; its activity is confined to the microvillar layer of the gastrodermis.
Digestion appears to be largely extracellular, as large volumes of haematin form in the gut lumen after haemolysis. However, this is supplemented by a significant amount of intracellular digestion: accumulations of iron-positive granules occur in approximately 20% of gastrodermal cells.
All gastrodermal cells are alike, and all can undertake the same intracellular digestive process. This is characterized by a number of morphologically distinct stages which have been studied using the electron microscope. The iron-positive particles distinguished under the light microscope were easily identifiable ultrastructurally. Spherical, weakly iron-positive bodies form within the cisternae of the endoplasmic reticulum. Phagosomes containing haemoglobin, or some breakdown product of haemoglobin, apparently bud off from the termini of a labyrinth system of tubules under the microvilli and fuse with the ER to form these phago-lysosomes. Intensely iron-positive heterolysosomes, also present in the cytoplasm of these cells, accumulate haemosiderin particles which are thought to be released into the cytoplasm during phago-lysosomal digestion.
The ensuing complex changes in cell morphology are, apparently, related to the elimination of spent phago-lysosomes. It has been suggested that the purpose of intracellular digestion is to provide a specific metabolite which the extracellular degradation of haemoglobin cannot supply.