Vinblastine-induced microtubular paracrystals in prolactin cells of anterior pituitary gland of lactating rats.

Vinblastine sulfate in physiological saline was injected directly into the pituitary glands of lactating rats. Injections were made through the ear canal using a syringe equipped with a 24-gauge needle. The animals were killed at 2, 4, or 6 hours after the injections. When the anterior pituitary glands were examined by electron microscopy, many microtubular paracrystalline deposits were seen in the prolactin and growth hormone cells. The usual cytoplasmic microtubules and microfilaments were not seen in the cytoplasm of these cells. Granular extrusion (exocytosis) was markedly depressed, and an accumulation of secretory granules was definitely observed in the prolactin cells after the administration of vinblastine.     

Scolex Glands Associated with the Rostella in Three Species of the Dilepididae (Cestoda: Cyclophyllidea)

The microanatomy, fine structure and cytochemistry of scolex glands of Vitta riparia, Angularella beema and Trichocephaloidis megalocephala are examined by light and electron microscopy. Cytochemical tests include PAS, mercury bromphenol blue and performic acid-alcian blue for light microscopy and periodic acid-thiocarbohydrazide-OsO₄ for electron microscopy. The scolex glands are organized in two spatially isolated syncytia, one located in the rostellum, the other in the rostellar sac. The cytoplasm of the gland syncytia is characterized by a high affinity for haematoxylin. Cytochemical tests indicate the presence of moderate amounts of glycoprotein in the glands. A specialized type of secretion—dark oval or ovoid bodies with diameter 0.3–0.5 μm are observed by EM in both the rostellum glands and the rostellar-sac glands of V. riparia and T. megalocephala , and in the rostellar-sac gland of A. beema . The rostellum gland of A. beema produces larger dark oval bodies measuring up to 0.9 μm. Lipid droplets are also observed in the glandular cytoplasm. Some tegumental cytons containing discoid bodies are found between the glandular perikarya. The glandular products and the lipid droplets are secreted via the rostellar tegument. © 1997 Published by Elsevier Science Ltd on behalf of The Royal Swedish Academy of Sciences.     

Salivary glands of <Emphasis Type="Italic">Amblyomma cajennense</Emphasis> (Acari: Ixodidae): a histological and an ultrastructural overview

The present study on the salivary glands of semi-engorged Amblyomma cajennense females has identified the various cell types present in this tissue and allowed its morphohistochemical characterization. Marking techniques were applied to detect polysaccharides (PAS), proteins (bromophenol blue), lipids (Nile blue) and calcium (von Kossa), as well as those of scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results obtained by TEM showed and confirmed that these individuals’ glands are also formed by round acini that are connected to the common excretory duct through acinar and intermediate ducts. Histological data as well as ultrastructural ones showed that the glands are formed by types I, II and III acini. In this study with salivary glands polysaccharides, proteins, lipids and calcium were observed in the cytoplasm and/or cell secretion granules—both free or forming complexes, as the intensity of the marking varied according to the cell as well as the type of acini analyzed, showing the structural and functional complexity of the tick salivary glands, characteristics that give the multifunctional character to this organ.     

Occurrence of unusual heterogeneous lipid-containing granule-storing cells in the main excretory duct epithelium of the male mouse submandibular gland

Summary The fine structure of the main excretory duct epithelium of the male mouse submandibular glands was investigated by scanning and transmission electron microscopy. Three principal cell-types were observed: type I and II, and basal cells. This epithelium was characterized by the presence of intercellular canaliculi. Type-I cells were the most numerous. They had an abundance of mitochondria, well-developed Golgi apparatus, a few electron-lucent lipid-containing granules and poorly developed basal infoldings. These cells were also characterized by many glycogen granules throughout the cytoplasm and abundant smooth endoplasmic reticulum in the apical cytoplasm. Type-II cells were the second most numerous. Their most characteristic feature was the presence of abundant heterogeneous lipid-containing granules having acid phosphatase activity at the periphery. They were concentrated in the infra- and supranuclear cytoplasm. The granules may be derived from mitochondrial transformation and seem to be a special kind of secondary autolysosome. Type-II cells also contained abundant mitochondria throughout the cytoplasm, much smooth endoplasmic reticulum in the apical cytoplasm, a well developed Golgi apparatus adjacent to the heterogeneous lipid-containing granules and no basal infoldings. Basal cells were situated adjacent to the basal lamina. They had a large nucleus and the cytoplasm was filled with glycogen granules.     

The morphology and ultrastructure of “amphipod silk” glands in <Emphasis Type="Italic">Ampithoe rubricata</Emphasis> (Crustacea,Amphipoda, Ampithoidae)

The anatomy and ultrastructure of “amphipod silk” glands in Ampithoe rubricata Montagu 1818 (Ampithoidae) have been studied. The morphology and ultrastructure of the glands in pereopods 3 and 4 have been examined in semithin and ultrathin sections using light and transmission electron microscopy. The glands of two types producing secretions different in their chemical compositions are observed in these pereopods. The ducts of the glands of both types lead to a common reservoir in the dactylus. Each gland comprises several secretory cells and one duct cell. The structure earlier regarded as the chitin wall of the duct is the cytoplasm of the duct cell; the presence of this cell in the studied glands is demonstrated for the first time. The secretory cells contain one or two nuclei and form rows along each duct cell. A new, previously unknown type of crustacean glands is described.     

The clypeal glands of Mynoglenes and of some other linyphiid spiders

The clypeal glands of three New Zealand Linyphiidae currently placed in Mynoglenes are described, by light, scanning and transmission electron microscopy. Shallow sulci beneath the lateral eyes of both sexes trap secretions which are produced by greatly elongated cells packed radially with respect to a given sulcus, and each voiding its product to the exterior by an individual ductule. The function of the secretion is unknown, although the ultrastructure of the gland resembles that of the defensive glands of many insects, but there is no separate duct cell, and the basal region of each secretory cell exhibits a unique strategy of membrane amplification, which divides the cytoplasm longitudinally into compartments by folds of the plasma membrane, compartments being still further subdivided into "tails". Patterns of vacuolation observed in various regions of the cytoplasm support the hypothesis that these unusual structures may be concerned with rapid water transport from the haemocoele, and that the cells discharge their contents by a "flush-out" mechanism. It is shown that male Erigoninae with cephalic specializations have similar clypeal glands, but with cytological profiles (in alcohol-fixed material) which suggest that special forms of membrane amplification are not present. Glands are absent in female Erigoninae, and in males with unmodified heads. It is suggested that in this latter subfamily the cephalic modifications may serve as presenting surfaces for sexual pheromones.     

Immunoelectron microscopic localization of epidermal growth factor in the eccrine and apocrine sweat glands.

We studied the localization of the epidermal growth factor (EGF) in eccrine and apocrine sweat glands with light microscopic and electron microscopic immunohistochemistry. Anti-human EGF (anti-hEGF) polyclonal antiserum and anti-hEGF monoclonal antibody (MAb) were used for the study. Light microscopic immunohistochemistry with monoclonal and polyclonal antibodies showed that hEGF-like immunoreactivity was strongly positive in the myoepithelial cells and weakly positive in the secretory cells of eccrine sweat glands. In apocrine sweat glands, it was strongly positive in the secretory cells as well as in the myoepithelial cells. Immunoelectron microscopy with polyclonal antibody showed that hEGF-like immunoreactivity was present in secretory granules of apocrine secretory cells. These granules had mitochondrion-like internal structure. No reactivity was observed on the eccrine secretory cells by immunoelectron microscopy. Neither dark cell granules nor mitochondria in eccrine secretory cells were labeled with anti-hEGF antibody. In both eccrine and apocrine sweat glands, hEGF-like immunoreactivity was diffusely present in the cytoplasm of myoepithelial cells. However, nuclei and mitochondria of myoepithelial cells were devoid of immunoreactivity for hEGF. Our observations indicate that apocrine sweat glands may secrete more hEGF in the sweat than eccrine sweat glands.     

Mandibular glands of male European beewolves, Philanthus triangulum (Hymenoptera, Crabronidae)

Males of a solitary digger wasp, the European beewolf, Philanthus triangulum, possess large mandibular glands that have been reported to produce a scent marking pheromone. We analysed the morphology and ultrastructure of these glands using light microscopy as well as scanning and transmission electron microscopy. The paired glands are located laterally in the head and each side consists of a larger and a smaller part. Both parts possess a collecting duct each with distinct openings at the mandible base. However, the collecting duct of the larger part is additionally connected to the pharynx through a lateral extension. The collecting ducts are bordered by a monolayered epithelium lined with cuticle that exhibits conspicuous ramified protuberances. About 1400 acini consisting of class 3 gland cells surround the ducts and are connected to them through conducting canals. The main components in the cytoplasm of these gland cells are mitochondria, well-developed smooth endoplasmatic reticulum, and electron lucent vesicles suggesting a high secretory activity. The connection between the large gland parts and the pharynx suggests that the secretion of the mandibular glands might not only be delivered directly onto the mandibles but might also be transported to and stored in the postpharyngeal gland.     

Calcitonin gene-related peptide-like immunoreactive cells in the secretory portions of rat sweat glands

Summary We found cells with calcitonin gene-related peptide-like immunoreactivity and with many cored vesicles in the secretory portions of sweat glands of rat foot pads. About 10% of sweat glands contained single immunoreactive cells. The immunoreactive cells were flaskshaped, with a narrow apex facing the glandular lumen and the bulk of the cell body in the basal half of the glandular wall. In the cytoplasm, there were many vesicles, 100–250 nm in diameter, with cores of various electron densities. These cytochemical and cytological characteristics suggest that the immunoreactive cells are homologous to gastrointestinal basal granulated cells.     

Structure and ultrastructure of leaf and calyx glands in Galphimia brasiliensis (Malpighiaceae)

The present study describes the anatomical structure of calyx and leaf glands in Galphimia brasiliensis and analyzes the mechanism of secretion. The glands are marginal and suprabasal, cup-shaped, sessile, and scarcely visible with the naked eye. Light microscopy reveals the following features: a thin, smooth cuticle; unistratified secretory cells; subglandular parenchyma; and vascular bundle supply composed of phloem and xylem with abundant druses of calcium oxalate. Transmission electron microscopy reveals the presence of secretory cells with conspicuous nuclei, dense cytoplasm, lipid droplets, numerous vesicles, mitochondria, Golgi, rough endoplasmic reticulum (RER), and elongated plastids with osmiophilic contents. The secretion reaches the apoplastic space and accumulates beneath the cuticle. Finally, the viscous, translucent exudate is eliminated by mechanical rupture of the cuticle. Histochemical analysis confirms that lipids are the main constituent. Small amounts of polysaccharides were also identified.     

The cytology of apocrine sweat glands

Summary The secretory cells of human apocrine sweat glands are characterized by the presence of large mitochondria, which have scant cristae and an electron opaque matrix. Electron opaque granules, presumed to be a keratin, are present in the supranuclear cytoplasm. The keratin granules contain histochemically demonstrable SH, SS, and lipid groups, and they have a typical appearance by electron microscopy. Secretory vacuoles containing mucopolysaccharide are formed in association with the Golgi apparatus and are liberated from the cytoplasm by a merocrine mechanism. The duct cells of human apocrine glands contain few organelles and are presumed to alter the secretion little, if at all. The term apocrine should be retained, although the cells secrete by a merocrine mechanism, and used in a generic sense to designate a defined group of epidermally derived glands.This investigation was supported in part by Public Health Service research grants GM-03784 and GM-10102 from the Institute of General Medical Sciences.     

Cells with unusual mitochondria in the thyroid gland of an old rat]

Thyroid glands of 3 year old rats have been studied by electron microscopy. The cells with changed mitochondria were found next to the typical thyrocytes in the follicle walls. The large mitochondria with dense matrix and tubular cristae often occupy the major part of the cytoplasm in these cells. On this basis, the author considers the changed cells to be the Askanazy cells, or oncocytes. Mitochondria-rich cells were found also among calcitocytes. The origin of oncocytes from usual thyrocytes and calcitocytes is under discussion.     

Morphology of the granular secretory glands in skin of poison-dart frogs (Dendrobatidae)

The granular glands of nine species of dendrobatid frogs were examined using light and electron microscopy. The glands are surrounded by a discontinuous layer of smooth muscle cells. Within the glands proper the secretory cells form a true syncytium. Multiple flattened nuclei lie at the periphery of the gland. The peripheral cytoplasm also contains mitochondria, rough surfaced endoplasmic reticulum, the Golgi apparatus, and an abundance of smooth endoplasmic reticulum. Centrally, most of the gland is filled with membrane-bound granules surrounded by amorphous cytoplasm. Few other organelles are found in this region. Early in the secretory cycle, the central part of the gland is filled with flocculent material which appears to be progressively partitioned off by membranes to form the droplet anlage. As granules form, the structure of the contents becomes progressively more vesicular. Dense vesicles, which bud off from the Golgi apparatus, fuse with the granular membrane during the development of granules, and might contain enzymes involved in toxin synthesis. The granules at this point resemble multivesicular bodies. Their structure is similar in all species of dendrobatid frogs even though the different frogs secrete substances of different chemical structure and toxicity.     

Programmed cell death in the larval salivary glands of <Emphasis Type="Italic">Apis mellifera</Emphasis> (Hymenoptera,Apidae)

The morphological and histochemical features of degeneration in honeybee (Apis mellifera) salivary glands were investigated in 5th instar larvae and in the pre-pupal period. The distribution and activity patterns of acid phosphatase enzyme were also analysed. As a routine, the larval salivary glands were fixed and processed for light microscopy and transmission electron microscopy. Tissue sections were subsequently stained with haematoxylin-eosin, bromophenol blue, silver, or a variant of the critical electrolyte concentration (CEC) method. Ultrathin sections were contrasted with uranyl acetate and lead citrate. Glands were processed for the histochemical and cytochemical localization of acid phosphatase, as well as biochemical assay to detect its activity pattern. Acid phosphatase activity was histochemically detected in all the salivary glands analysed. The cytochemical results showed acid phosphatase in vesicles, Golgi apparatus and lysosomes during the secretory phase and, additionally, in autophagic structures and luminal secretion during the degenerative phase. These findings were in agreement with the biochemical assay. At the end of the 5th instar, the glandular cells had a vacuolated cytoplasm and pyknotic nuclei, and epithelial cells were shed into the glandular lumen. The transition phase from the 5th instar to the pre-pupal period was characterized by intense vacuolation of the basal cytoplasm and release of parts of the cytoplasm into the lumen by apical blebbing; these blebs contained cytoplasmic RNA, rough endoplasmic reticule and, occasionally, nuclear material. In the pre-pupal phase, the glandular epithelium showed progressive degeneration so that at the end of this phase only nuclei and remnants of the cytoplasm were observed. The nuclei were pyknotic, with peripheral chromatin and blebs. The gland remained in the haemolymph and was recycled during metamorphosis. The programmed cell death in this gland represented a morphological form intermediate between apoptosis and autophagy.     

Ultrastructure of the cardiac and pyloric glands of the gastric mucosa of the South African hedgehog,Atelerix frontalis

The cardiac and pyloric glands in the gastric mucosa of the South African hedgehog, Atelerix frontalis, are described. The cardiac area of the stomach contains proper cardiac glands and lacks undifferentiated fundic glands. The cardiac glands are simple tubular, coiled, and lined with columnar cells ultrastructurally similar to those of the gastric surface epithelium. Secretory granules with varying electron densities fill the apical cytoplasm of these cells. In contrast to other mammals, these glands lack mucous neck cells. The neck of the pyloric glands contains only a single cell type, whereas the basal regions of these glands contain “light” and “dark” cells. The secretory granules in the “dark” cells and the pyloric neck cells have a moderate electron density and often contain an electron dense core. An electron-lucent cytoplasm with numerous polysomes is characteristic of the “light” cells. Some “light” cells contain electron-dense granules in the apical cytoplasm. The presence of only neutral mucins in the cardiac gland cells denotes the absence of mucous neck cells. The acidic mucins within the pyloric neck cells seem to indicate that these cells are mucous neck cells, whereas the neutral mucins within the basally located pyloric gland cells show at least a partial functional difference from the pyloric neck cells. © 1993 Wiley-Liss, Inc.     

Fine structure of the spiracular glands in larval Drosophila melanogaster (Meig.) (Diptera : Drosophilidae)

The spiracular glands in the third-instar larvae of Drosophila melanogaster (Diptera : Drosophilidae) were examined with light and electron microscopy. Three club-shaped, unicellular glands are associated with each spiracle. Each gland has a large nucleus with a well-developed nucleolus and polytene chromosomes. Cytoplasmic features include a prominent plasma membrane reticular system (PMRS), which contains electron-dense material and gives rise to endocytotic vesicles. Numerous lipid droplets, mitochondria, free ribosomes, glycogen, lysosomes, and vesicles are scattered throughout the cytoplasm. The smooth endoplasmic reticulum is abundant, but rough endoplasmic reticulum and Golgi complexes are sparse. Small lipid droplets appear to fuse with one another to form larger droplets. In late third-instar glands, normal mitochondria decrease in number; they appear to degenerate and become converted into dense bodies with finely granular interiors. Several microvillous channels containing lipid are present within the cytoplasm. In the lumina of most of these channels are found the distal tips of cuticular ductules. The cuticular ductules merge with one another dorsally to form the main duct that carries the lipoid secretion to the spiracle cleft. The ultrastructure of the spiracular glands is consistent with their roles in the synthesis of lipoid secretion, which is used to provide hydrophobicity of the surface and to trap small particulate matter.     

An ultrastructural study of the cysts in chicken ultimobranchial glands,with special reference to C-cells

Summary The ultimobranchial glands of the chicken were examined by electron microscopy and immunocytochemistry using a calcitonin antiserum. Electron microscopy confirmed the presence of C-cells, containing numerous secretory granules storing calcitonin, in the luminal lining of cyst-like structures found in these glands. These cells were furnished with prominent microvillar projections at their luminal surface, and the cytoplasm of the apical region was filled with fibril material. Furthermore, the cells contained prominent junctional complexes and desmosomes at their apico-lateral surfaces. In these C-cells, secretory granules were concentrated near the lumen and some were attached to the apical cell membrane. The luminal content of the cysts had a colloid-like and flocculent appearance, and was frequently seen attached to the cytoplasmic projections or apical cell membrane of the C-cells. Since the cysts progressively increase in volume and number with age, it is suggested that they may partly play a role in the storage of excess or unneeded hormonal products.     

The morphology and ultrastructure of salivary glands of Zoraptera (Insecta)

The salivary glands of two species of Zoraptera, Zorotypus caudelli and Zorotypus hubbardi, were examined and documented mainly using transmission electron microscopy (TEM). The results obtained for males and females of the two species are compared and functional aspects related to ultrastructural features are discussed. The salivary glands are divided into two regions: the secretory cell region and the long efferent duct, the latter with its distal end opening in the salivarium below the hypopharyngeal base. The secretory region consists of a complex of secretory cells provided with microvillated cavities connected by short ectodermal ducts to large ones, which are connected with the long efferent duct. The secretory cell cytoplasm contains a large system of rough endoplasmic reticulum and Golgi apparatus producing numerous dense secretions. The cells of the efferent duct, characterized by reduced cytoplasm and the presence of long membrane infoldings associated with mitochondria, are possibly involved in fluid uptaking from the duct lumen.     

Olfactory mucosa ultrastructure in the short-tailed shrews,Blarina brevicauda and Blarina carolinensis

The olfactory mucosae of the northern short-tailed shrew, Blarina brevicauda, and the southern short-tailed shrew, Blarina carolinensis, were examined by light and electron microscopy. A well-developed olfactory epithelium was observed that included all of the cells necessary to provide for a sensitive olfactory system, suggesting that olfaction plays a major role in the behavior of these animals. There were no significant differences between the olfactory mucosae of these two species. The general features of the olfactory epithelium in these shrews were similar to those reported for several other macrosmatic mammals. A new type of supporting cell, called the light supporting cell, was observed in these shrews. The light supporting cell cytoplasm exhibited very little staining by light microscopy and had low electron density by transmission electron microscopy compared to that of the more common dark supporting cell. The light supporting cell had a convex apical surface with microvilli and lacked the large amounts of smooth endoplasmic reticulum (SER) typical of the apical cytoplasm of the dark supporting cell. In the lamina propria of the mucosa, the Bowman's glands consisted of two cell types, one with electron-lucent, alcian blue-positive granules, and the other with electron-dense PAS-positive granules. The cell with electron-lucent granules contained large amounts of SER and small clumps of rough ER. The cells with electron-dense granules had large amounts of RER and little SER.