Ultrastructure of the protonephridial system, of Anoplodiscus cirrusspiralis (Monogenea Monopisthocotylea).

The flame bulb is formed by a terminal cell and a proximal canal cell. The weir consists of interdigitating ribs all of which form one circle, i.e. alternating ribs do not have distinctly 'internal' or 'external' positions. Cytoplasmic cords are absent and all ribs, i.e. those continuous with the proximal canal cell and those continuous with the terminal cell, form external leptotriches. At least some external leptotriches have interconnected branches extending along the flame bulb. Internal leptotriches are not branched and arise from the basal perikaryon of the terminal cell. In the cytoplasmic cylinder at the tip of the flame bulb, structures resembling incomplete septate junctions were seen. However, neither the cytoplasmic cylinder nor the small protonephridial capillaries contain complete septate junctions as found in all other Monogenea Polyopisthocotylea, Monogenea Monopisthocotylea, Trematoda Aspidogastrea and Trematoda Digenea examined to date. In the lack of a septate junction, Anoplodiscus resembles Udonella, Amphilinidea, Gyrocotylidea and Eucestoda. However, the presence in this species of rudimentary septate junctions in the small capillaries and of complete junctions in larger ones indicates that complete junctions have been secondarily lost. Anoplodiscus resembles the Monogenea and Trematoda in the presence of lamellae in the larger protonephridial ducts. For the first time in a monogenean, the ultrastructure of the excretory bladder is described. A nucleated convoluted duct opens through a narrow connecting duct into the bladder, which in turn opens through a narrow connecting duct into the excretory pore lined by tegument. Convoluted duct, connecting ducts and bladder are lined by a lamellated epitheliu.(ABSTRACT TRUNCATED AT 250 WORDS)     

Morphology of urogenital system in female Echinopardalis atrata (Acanthocephala)

Four major areas of the urogenital system of Echinopardalis atrata are examined: (1) capsular protonephridial system, (2) uterine bell complex, (3) uterus, (4) vagina. Photomicrographs of cross sections from wax preparations depict morphological changes along the length of this system. Diagrammatic illustrations show relationships between excretory ducts and oviducts in the uterine bell complex. Relative positions of dorsal and ventral ligament accessory cells, median wall cells, and sheathing syncytium are also shown in this complex. The common oviduct and excretory canal join to form a ciliated urogenital canal that empties into the lumen of the uterus along the latter's anterior mid-dorsal surface. The excretory bladder is located on the inside mid-dorsal surface of the bell wall and is serviced by 2 nephridial canals--1 from each of 2 capsular protonephridia. The vagina affixes the posterior terminus of the uterus to the tegument and consists of an internal and external sphincter surrounding a hypodermal lining.     

Ultrastructure of the male accessory ducts and prostate gland of Diclidophora merlangi (Monogenoidea)

The vas deferens, seminal vesicle, penis and common genital atrium of the monogenean, Diclidophora merlangi are lined by a very flat, lamellate epithelium. The structure is apparently syncytical, although nuclei or perikaryons have not been observed. The epithelium extends to just inside the gonopore where a septate desmosome marks the union with body tegument. There is minor regional variation in structure. The terminal portion of the seminal vesicle and the penis lumen are lined in part by the luminal cytoplasm of the prostate gland which surrounds this part of the reproductive tract. The prostate gland cells are synthetically active and produce a characteristic secretory body that is released either singly by exocytosis, involving membrane fusion, or in bulk via apocrine secretion. The secretion is acidophilic, PAS-positive and reactive for protein. The penis is sucker-like in structure and armed with a ring of 16 genital hooklets. Cilia have not been observed in any part of the male reproductive tract, and sense receptors are not apparent in the tegument surrounding the gonopore.     

Fasciola hepatica: the ultrastructure of the epithelium of the seminal vesicle, the ejaculatory duct and the cirrus.

The ultrastructure of the seminal vesicle, ejaculatory duct, cirrus sac and cirrus is described. The epithelium of the seminal vesicle consists of a single layer of squamous to cuboidal cells. The apical ends of the cells have thin polymorphic lamellae and long narrow pits, both of which enclose normal spermatozoa. The cells have a moderate amount of GER and Golgi complexes which produce a lucid secretory body. The ejaculatory duct epithelium is composed of cuboidal to columnar cells between or through which project the terminal parts of the ducts of the unicellular prostate glands. The apical surfaces of the epithelia are extended into triangular or filiform projections having thin sinuous lamellae. The cytoplasm contains GER cisternae and Golgi complexes which synthesize a dense ovoid secretion. The cirrus sac and cirrus are covered by a thin modified tegument. The cirrus has many spines and the normal ratio of T1 and T2 type of secretory bodies, whereas the cirrus sac has few spines and the T2 type of secretory body predominates over the T1 type. The significance and possible functions of the structures observed in the three tissues are discussed.     

An ultrastructural study of alimentary tract development in the cercariae of Prosorhynchoides borealis (Digenea,Bucephalidae)

Podvyaznaya I. 2011. An ultrastructural study of alimentary tract development in the cercariae of Prosorhynchoides borealis (Digenea, Bucephalidae). —Acta Zoologica (Stockholm) 92 : 170–178. The development of digestive system in Prosorhynchoides borealis cercariae was studied using transmission electron microscopy. The foregut and caecum primordia arise in early cercarial embryos as two adjoining cellular cords. The primordial pharynx appears as a cluster of myoblasts in the mid‐part of the foregut primordium whose proximal end abuts onto the ventral embryonic tegument. Later, a lumen develops within the gut primordia and their component cells form the embryonic cellular epithelium with an essentially similar structure in the foregut and caecal regions. Subsequently, the foregut epithelial cells merge to form a syncytium. This process proceeds asynchronously and the most proximal foregut area remains cellular for the longest time. The syncytial lining of the foregut establishes syncytial connections with secretory cytons differentiating in the surrounding parenchyma. These cytons produce secretory granules, which are transported through cytoplasmic connections to the foregut syncytium. Before cercariae reach maturity, their foregut epithelium becomes anucleate and continuous with the external tegument. By the end of cercarial development, numerous short lamellae appear on the luminal surface of the caecal epithelium. The caecal cells become involved in secretory activity as indicated by the presence of Golgi‐derived secretory bodies in their cytoplasm.     

Studies on host specificity in Paragonimus westermani: II. Histochemical and cytochemical characterization of metacercariae and worms from rats and dogs

Histochemical tests were done on newly excysted metacercariae and worms recovered from an abnormal host (rat) and the definitive host (dog) for some oxidoreductases, phosphatases and glycosidases. The results demonstrate that rat worms have enzymatic distribution and intensities more similar to those of metacercariae than to adult worms from dogs. Ultracytochemical examination of acid and alkaline phosphatase and Mg-ATPase activity was also carried out. Acid phosphatase activity occurred exceptionally in the excretory bladder and caeca of dog worms. No activity was observed in rat worms except for lysosomal granules in the tegument. Alkaline phosphatase activity was exhibited in the excretory bladder in both dog and rat worms. Mg-ATPase activity occurred in the tegument and parenchymal cells in dog worms and in the excretory bladder in rat worms. In metacercariae, little or no reaction for these enzymes was present except for Mg-ATPase activity on the excretory ducts. These observations, together with the histochemical results, indicate that metabolic activity in rat worms is higher than in metacercariae although it is strongly reduced compared with dog worms.     

Electron microscope studies of Fasciola hepatica. 13. Fine structure of newly excysted juvenile

The gross morphology and fine structure of the newly excysted juvenile fluke are described. The tegument is organized as in the adult, with a spine-containing surface syncytium connected to a perinuclear region lying below the muscle layers. It differs from the adult, however, in having only one type of perinuclear region and one type of secretory body. The digestive system has all the morphological characteristics of a secretory epithelium, rather than an absorptive one. It has numerous dense secretory bodies, ribosomes, and GER, an irregular apical surface due to eccrine secretion, and a lumen filled with a moderately dense material derived from the dispersed secretory granules.The excretory system closely resembles that of the adult, but has, in addition, part of its ascending ducts ciliated and concretions as well as lipid droplets as visible excretory products. The muscle is identical with that of the adult and the parenchyma is also very similar to the adult, although it has more lipid droplets and is associated in a less complex way with cells of other organ systems. Groups of embryonic cells are present and are characterized by a dense, invaginated nucleus surrounded by a very thin layer of cytoplasm.     

Distribution and ultrastructure of two types of scolex gland cells in adult Proteocephalus macrocephalus (Cestoda, Proteocephalidea)

In the scolex-neck region of the adult Proteocephalus macrocephalus two types of eccrine gland cells are present. The first type of gland cells, localized in the frontal part of the scolex only, contains large, more or less round electron lucid granules. The second type of unicellular glands produces large electron dense granules. These electron dense granular gland cells are localized primarily in the neck region, only few are present in the scolex apex. The secretion of both types of gland cells is concentrated in the ducts opening to the exterior. The ducts are fixed to the plasmalemma of the tegument by septate junctions. The function of both types of gland cells is discussed.     

Electron microscope studies of Fasciola hepatica III. Fine structure of the prostate gland.

An ultrastructural study of the prostate gland of Fasciola hepatica shows it to be composed of numerous unicellular glands. These gland cells contain an extensive granular endoplasmic reticulum (GER) system parts of which are intimately associated with septum-like invaginations of the plasma membrane extending almost to the nucleus. Also associated with the GER are many Golgi complexes which secrete large electron-lucid carbohydrate-rich secretory vesicles. The secretion passes up the gland ducts along with a very dense granular and fibrillar material. The ducts have a peripheral microtubular skeleton and are tightly bound to the epithelium of the ejaculatory duct by septate desmosomes. Secretory vesicles are stored in the expanded ends of the ducts where they pass through the ejaculatory epithelium and their content is discharged by the bursting of their limiting membrane.     

Junctional types in the tissues of an onychophoran: the apparent lack of gap and tight junctions in Peripatus

The Onychophora are a rare group of primitive invertebrates, relatively little investigated. Tissues from a range of their digestive, secretory and excretory organs have been examined to establish the features of their intercellular junctions. Glutaraldehyde-fixed cells from the midgut and rectum, as well as the renal organ, mucous gland, salivary gland, epidermis, CNS and testis from specimens of Peripatus acacioi, have been studied by thin section and freeze-fracture electron microscopy. Adjacent cells in the epithelia of all these tissues are joined by apical zonulae adhaerentes, associated with a thick band of cytoskeletal fibrils. These are followed by regular intercellular junctional clefts, which, in thin sections, have the dense, relatively unstriated, appearance of smooth septate junctions (SSJ). However, freeze-fracture reveals that only the midgut has what appear to be characteristic SSJs with parallel alignments of closely-packed rows of intramembranous particles (IMPs); these IMPs are much lower in profile than is common in such junctions elsewhere. The mucous gland, testis, rectal and renal tissues exhibit, after freeze-fracture, the characteristic features of pleated septate junctions (PSJ) with undulating rows of aligned but separated junctional particles. Suggestions of tricellular septate junctions are found in replicas at the interfaces between 3 cells. In addition, renal tissues exhibit scalariform junctions in the basal regions of their cells. Between these basal scalariform and apical septate junctions, other junctions with reduced intercellular clefts are observed in these renal tissues as well as the rectum, but these appear not to be gap junctions. Such have not been unequivocally observed in any of the tissues studied from this primitive organism; the same is true of tight junctions.     

Fine structure of the protonephridial system in planaria

Summary Distal to the flame cells, the protonephridial tubules of fresh-water planarians are circumferentially composed of at least two cells attached by septate junctions; and may be divided, on the basis of morphological criteria, into three longitudinal regions. The cells of nonciliated ductules and ciliated collecting ducts appear to be absorbing material from the lumen; and a distinct proximal-distal polarity is present in each individual cell. At the proximal pole are concentrated micropinocytotic caveolae with amorphous and structural coats on the luminal and cytoplasmic surfaces, respectively. Proceeding distally, a Golgi complex is situated between the micropinocytotic vesicles and large, basophilic, paracrystaline granules. This unusual polarity is interpreted to be important to the resorptive function of the cells.In four areas of the worm, the branched collecting ducts combine to form single osmoregulatory (O. R.) ducts. The O. R. cells have many mitochondria located in slender processes formed by basal and lateral invaginations and interdigitations. The adjacent plasmalemmas of normally fixed cells are separated by a 180 Å gap; but higher tonicity fixative shrinks the cells, increasing the apparent extracellular space. The O. R. cells differ from analogous cells in higher animals in their function as an osmoregulatory epithelium in the absence of a basement membrane.This investigation was supported by NIH Pre-doctoral Training Grant 5T1 GM 723-07.The author is grateful for the interest and guidance of Dr. Orin M. Lofthus and Dr. David B. Slautterback; and is pleased to acknowledge the generous support of undergraduate research by the President and Fellows of Carleton College, Northfield, Minnesota which made possible the initial stages of this work.     

Ultrastructure of the copulatory organ of Haplopharynx quadristimulus and its phylogenetic significance (Plathelminthes,Haplopharyngida)

Summary The male reproductive system in Haplopharynx quadristimulus consists of paired testes, sperm ducts, seminal vesicles, seminal ducts, a copulatory organ containing prostatic vesicle and stylet apparatus, and the male canal. By electron microscopy all components appeared to be regional specializations of a canal extending from the testes to the body wall and lined by a multiciliated epithelium. The epithelium of the stylet apparatus contained six different cell types. One cell type (matrix syncytium) formed the stylet and the other five were located distal to the stylet/prostatic-vesicle junction along the male system epithelium. Each cell type was attached to the supporting intercellular matrix at a different level along the stylet apparatus. All cell types extended to the distal end of the stylet apparatus regardless of where they originated along its length. The cells in the apparatus lacked cilia, but one of the cell types contained rootlets. Modified rootlets or rootlet derivatives were possibly present in another cell type in the form of rootlet-like ribbons. The findings support the monophyly of the Macrostomida Haplopharyngida (by common occurrence of a matrix syncytium) and at the same time suggest their separation as two distinct taxa (by differences in the structure of the prostatic vesicle and other parts of the stylet apparatus).Abbreviations a accessory spine - c circular muscle - ce centriole - ci cilium - di dictyosome - e epithelial cell - ed ejaculatory duct - ep epidermal cell - f rootlet-like ribbon - g prostatic gland cell neck - g1 type I gland cell granules - g2 type II gland cell granules - g3 type III gland cell granules - h hemidesmosome - i intercellular matrix - im internal muscle - j septate junction - l stylet apparatus lumen - le spine lateral extension - lm longitudinal muscle - m matrix syncytium - mc male-canal epithelial cell - me male canal - mp male pore - mt microtubules - mv microvilli - n nucleus - nc nerve cell body - np nerve process - om oblique muscle - p prostatic vesicle epithelial cell - pv prostatic vesicle - r rootlet - s stylet - sa stylet apparatus - sc sensory receptor - sd sperm duct - se seminal duct - sl stylet lumen - sp spot desmosome - sr sperm - sv seminal vesicle - t terminal web - te testis - u ultrarhabdite - z zonula adhaerens - 2 cell type 2 - 3 cell type 3 - 4 cell type 4 - 6 cell type 6     

The seminal vesicle of the African catfish,Clarias gariepinus

Summary The seminal vesicle of the African catfish, Clarias gariepinus, consists of 36–44 fingerlike lobes built up of tubules in which a fluid is secreted containing acid polysaccharides, acid-, neutral- and basic proteins, and phospholipids. In this fluid sperm cells are stored. The seminal vesicle fluid immobilizes the sperm cells. After ejaculation, it prolongs the period of sperm activity. The seminal vesicle fluid is secreted by the epithelium lining the tubules. The tubules in the proximal part of the lobes are predominantly lined by a simple cylindrical and those of the distal part by a simple squamous epithelium. These epithelial cells contain enzymes involved in energy-liberating processes, the enzyme activites being proportional to the height of the cells. Interstitial cells between the tubules have enzyme-histochemical and ultrastructural features indicative of steroid biosynthesis. Similar characteristics are found in testicular interstitial cells. The most rostral seminal vesicle lobes and the most caudal testicular efferent tubules form a network of tubules that opens at the point where the paired parts of the sperm ducts fuse with each other. The tubules of most seminal vesicle lobes, however, form a complex system that fuses with the unpaired part of the sperm duct.     

Ultrastructure of the anterior alimentary tract of a monogenean, Diclidophora merlangi

The anterior alimentary tract of Diclidophora merlangi is composed of a complex series of morphologically distinct epithelia interconnected by septate desmosomes and penetrated by the openings of numerous unicellular glands. The mouth and buccal cavity are lined by an infolding of modified body tegument, distinguished by uniciliate sense receptors, buccal gland openings, and in the buccal region by a dense, spiny appearance. The prepharynx is covered by an irregularly folded epithelium and, for part of its length, by the luminal cytoplasm of the prepharyngeal gland cells. The epithelium is syncytial and pleiomorphic, and regional variation in structure is common. A separate epithelium invests the lips of the pharynx and its free surface is greatly amplified by numerous, dense lamellae of varying dimensions. The lip epithelium is continuous with cytoplasmic processes of cells located external to the pharynx. A further, distinct epithelium borders the pharynx lumen and is composed of discrete cytoplasmic units connected by short septate desmosomes. The oesophagus is lined by a modified caecal epithelium, lacking haematin cells, and, in places, is perforated by the openings of oesophageal gland cells; it is continuous with the syncytial connecting tissue of the gut caeca.     

Ultrastructural observations on the redial tegument of Paramphistomum epiclitum from the planorbid snail, Indoplanorbis exustus.

The morphology of the tegument in the redia of Paramphistomum epiclitum (Digenea: Paramphistomidae) resembles that shown by most larval and adult digeneans; an outer surface syncytium is in continuity with the cytoplasm of in-sunken, nucleated cytons. Although tegumental cytons usually contain a single nucleus, some display up to six nuclei. The tegumental syncytium lining the pharynx of P. epiclitum rediae lack underlying cytons. The apical membrane of the tegument is elaborated by folds and microvilli, which presumably facilitate uptake of nutrients and/or exchange of ions involved in osmoregulation. A single type of secretory body, resulting from the fusion of smaller vesicles produced at Golgi complexes in the cytons, occurs throughout the tegument. Uniciliate sensory receptors occur in the surface syncytium particularly around the oral opening.     

Ultrastructure of the foregut and associated glands of Calicotyle kröyeri (Monogenea: Monopisthocotylea)

The mouth, pharynx and oesophagus of Calicotyle are lined by syncytial epithelia, and there are numerous unicellular glands associated with the oesophagus. An infolding of unmodified external tegument lines the mouth cavity and is connected by discrete cytoplasmic processes to subjacent perikarya. It contains two types of secretory body and its luminal surface is invested with a finely filamentous coating. The pharynx and oesophagus are lined by irregularly-folded epithelia that are interconnected by a septate desmosome. Membranous inclusions distinguish the pharynx epithelium and there is a well developed basal lamina for insertion of the pharyngeal muscles. The oesophagus epithelium is perforated by the openings of the oesophageal glands. These lie in the surrounding parenchyma and produce a dense, membrane-bound secretion which is conveyed by duct-like extensions of the glands to the oesophagus lumen. The ducts are supported in places by microtubules and are anchored to the oesophageal epithelium by septate desmosomes. A septate desmosome also marks the junction between the epithelium and the gut caeca.     

Ultrastructure of the tegument of the metacercaria of Timoniella imbutiforme

The spinous body tegument of the metacercaria of Timoniella imbutiforme (Molin, 1859) is described in detail and found to comprise an outer tegumental syncytium connected to subjacently situated subtegumentary 'cells'. There are four types of secretory bodies in the outer syncytial layer as well as serrated overlapping spines and mitochondria. The subtegumentary 'cells' are characterized by the presence of four secretory body types as well as giant bodies which may be involved in the elaboration of the secretory bodies or spine material. The normal configuration of the somatic muscles of T. imbutiforme show that the muscular machinery necessary for activity once the larval stage becomes excysted is already in place. The sensory endings are found to be of the uniciliate type occurring in groups of up to eight in raised domes distributed over the body. Secretory gland cells are numerous and possess long ducts connected to the basal lamina of the outer syncytial layer via septate desmosomes.     

Fasciola gigantica: Histology of the digestive tract and the expression of cathepsin L

The digestive tract of Fasciola gigantica is composed of the oral sucker, buccal tube, pharynx, esophagus, and caecum. The tegumental-type epithelium lines the first four parts of the digestive tract while the caecal-type epithelium lines the remaining parts from the caecal bifurcation. The caecal-epithelial cells are classified into 3 types according to their staining properties and ultrastructural characteristics, as related to the amount of food contents in the caecal lumen. All caecal-type epithelial cells synthesize and secrete cathepsin L, a major group of enzymes in the digestive tract, as detected by in situ hybridization and immunolocalization. Moreover, the secreted cathepsin L is also adsorbed on the outer surface of the tegument and the glycocalyx coating of the surface of the tegument, whereas the tegumental cells and tegumental syncytium covering the parasite’s body and lining the proximal part of the digestive tract exhibit no in situ hybridization signal and immunostaining for cathepsin L.     

Ultrastructure du canal des glandes agrégées et flagelliformes d'Araneus diadematus Clerck (Araneae,Araneidae)

Summary The excretory ducts of the silk glands which produce the viscid spiral of the webs ofAraneus diadematus show a complex structure. The duct of aggregate glands consists of three superposed types of cells. Several connective layers cover large and irregular nodule-forming cells which are rich in glycogen and mitochondria surrounded by invaginations of the plasma membranes. The internal cells, whose apical poles are lined by a cuticular intima, would be quite ordinary if not for the fact that they often carry large vacuoles which seem to empty themselves by exocytosis. Activity in the nodule cells is perceived from variations in the glycogen level and from the appearance of the mitochondria. Internal cells of the duct, when within the posterior spinneret, gradually acquire the characteristics of absorbing cells.The duct of flagelliform glands consists of two types of cells. The external cells, bounded by a simple basal lamina, are rich in mitochondria, glycogen, and invaginations of the plasma membranes; their activity is shown by variations in glycogen level and the extent of the extracellular spaces. The internal cells show numerous mitochondria either at the apical or basal poles, variable glycogen levels, long microvilli, and signs of apical absorption by pinocytosis; the sub-cuticular layer of the intima is particularly thick.We propose a functional interpretation of the aspects described above, and discuss it in terms of recent data on the chemical composition of silks. The excretory ducts are held to modify, by their activity, the secretory products of both types of glands. Solutes, especially phosphate ions, cross both cells and intima and would enter the glue of the aggregate glands which then undergoes partial dehydration in the posterior spinnerets. The product of the flagelliform glands seems to all appearance dehydrated during its passage in the duct and up to about the half-way through the posterior spinnerets. The liquid would flow through an extracellular path below the apical septate junctions of the internal cells. This study therefore favours attributing important role to the excretory ducts of silk glands in the final phase of the formation of silk fibres by spiders.     

A review of protonephridial excretory systems in Acanthocephala

Our present understanding of the excretory system of Acanthocephala is largely the result of work done by 5 German scholars: Kaiser, Schepotieff, Meyer, Kilian, and von Haffner. Present studies indicate that a protonephridial system is restricted to the family Oligacanthorhynchidae. However, many members of this family have not had a protonephridial system described. Three nephridial designs have been described: 1) dendritic type, organized as branches of a tree where each final branch terminates in a ciliated bulb; 2) capsular type, in which all ciliated bulbs empty directly into a common chamber; and 3) rudimentary type, consisting of a single cell with a patent ciliary pouch but no ducts to the outside. The first 2 types are a syncytia with 3 nuclei located in the capsule or stem wall and none in the flame bulbs. These excretory systems consist of 2 clusters of flame bulbs that empty separately into an expandable excretory bladder which in turn empties into ducts of the reproductive system. This urogenital system empties to the outside through a gonopore located at the tip of the penis in males and the posterior terminus of the vagina in females. Cilia occur in certain excretory tubes, depending on sex and species, but are unknown in the excretory bladder or ducts leading into it. The rudimentary type consists of a cell whose posterior extension terminates near the bursal lumen, but it is not known if this is significant for the discharge of material. There is no information on the physiology or biochemistry of the excretory system or its products.