Histopathological study of von Ebner's lingual salivary glands in Trypanosoma cruzi-infected mice

In the present study we describe the histopathological alterations induced by RC strain of Trypanosoma cruzi in the mouse von Ebner's lingual salivary glands during the acute period of infection: Amastigotes were found in von Ebner's gland acini cells, excretory duct cells, intralobular connective tissue, inside the acini lumen and muscle fibres. Desorganized parenchyma with impairment at the acinar and duct level, and intense lymphoplasmocytic infiltrate were seen.     

von Ebner's glands intercalated duct adenocarcinoma with PALB2 gene mutation

Secretory carcinoma of the salivary glands is a distinct entity with distinct morphologic features, immunohistochemical profile and molecular alterations. It mainly affects middle aged individuals with slight male predominance and parotid gland is the most common site of involvement. Although ETV6-NTRK3 gene fusion is considered pathognomonic for secretory carcinoma, advances in molecular profiling of this tumor have led to the discovery of novel ETV6 fusion partners and gene mutations. Herein, we describe a case of an adenocarcinoma of intercalated duct origin favor secretory carcinoma, in a unique location of von Ebner's glands of mobile tongue in a 40-year-old Caucasian female. Aside from being in a unique location, the tumor showed somatic mutation for PALB2 gene which has not been described so far in secretory carcinoma. Discovery of novel fusions and mutations have therapeutic implications with respect to targeted therapy.     

Expression of IGFBPs in the developing mouse submandibular and von Ebner's glands

The expression of insulin-like growth factor binding proteins (IGFBPs) in the developing mouse submandibular and von Ebner’s glands was determined by in situ hybridization and by an immunohistochemical method. In the submandibular glands, IGFBP-2 and IGFBP-4 mRNAs were expressed in the terminal end-buds (TEB) at E13–E17, concomitant with epithelial branching. IGFBP-3 mRNA was expressed in the mesenchyme surrounding the TEB; and IGFBP-5 mRNA, in the ducts. At E17, IGFBP-5 mRNA expression was observed not only in the ducts but also in the TEB. Similarly, IGFBP-4 mRNA expression was observed not only in the TEB but also in the mesenchyme. After birth, IGFBP-4 expression was observed only in the connective tissue and disappeared by P14. That of IGFBP-7 appeared at P1 and was observed in the connective tissue until P21. The IGFBP-5 mRNA expression pattern after birth was the same as that seen at E17, but at P21 IGFBP-5 was immunohistochemically expressed only in the duct. The mRNA level of IGFBP-2 expression at postnatal days was weak, but its protein was detected in the ducts and acini at P14–P21. In von Ebner’s glands, which appeared at the base of the circumvallate papillae at E17, only IGFBP-2 and IGFBP-4 mRNAs were expressed in the ducts and acini. Postnatally, IGFBP-4 was substituted by IGFBP-5 in the same region. Immunohistochemically, IGFBP-5 and IGFBP-2 were expressed in the ducts and acini at P14–P21. Throughout the study, IGFBP-6 was not detected by in situ hybridization, the immunoreactivity for it was observed in the nerve fibers of submandibular and von Ebner’s glands. These data support a role for these molecules as local mediators of salivary growth and differentiation.     

The effects of histamine,pyrilamine, cimetidine,and ranitidine on secretion of lingual lipase and amylase from rat von Ebner's glands

Minced von Ebner's glands of rat tongue were incubatedin vitro with histamine and histamine receptor antagonists. At various time intervals, media and homogenates of the tissue were assayed for lingual lipase and amylase activity and percentage secretion calculated. Histamine elicited moderate secretion (10%) of lingual lipase and amylase. In contrast, pyrilamine, and H₁ receptor antagonist, elicited>60% secretion. There were statistically significant differences between the percentage secretion of lingual lipase and amylase for basal secretion, as well as for histmine-and pyrilamine-evoked secretion of lingual lipase and amylase for basal secretion, as well as for histamine-and pyrilamine-evoked secretion above basal. The H₂ receptor inhibitors, cimetidine and ranitidine, stimulated secretion of only amylase, but not lingual lipase. When combined with histamine, these antagonists partially inhibited only the secretion of histamine-evoked lingual lipase, but not amylase. The differences in percentage secretion between the two enzymes indicate that exocytosis may not be the only process involved in protein secretion. The anomalous effects of the H₁ and H₂ receptor antagonists necessitate a more detailed characterization of the receptors of von Ebner's glands.     

Lipolytic activity of human lingual glands (Ebner)

Human tongue preparations contain lipolytic activity similar to that present in human esophageal and gastric aspirates and in serous glands of rat tongue. The activity is present in homogenates of the glandular region (Ebner) beneath the cirumvallate papillae, and in secretions collected from the trough of the papillae. The lipolytic enzyme hydrolyzes long chain triglycerides to partial glycerides (di- and monoglyceride), glycerol, and free fatty acids at pH optimum 5.4. Lipolytic activity, expressed as nanomoles of triglyceride hydrolyzed per minute was in the range of 0 to 500 per gm. of tongue homogenate and 78 to 277 per ml. of aspirate from the vallate papillae. There was a 50% inhibition of the lipolytic activity by 4 mM sodium taurodeoxycholate. Specimens obtained from the region of the vallate papillae were examined by light and electron microscopy. Electron-dense granules similar to secretory granules present in rat Ebner's gland and in serous acini of human submaxillary glands were detected. Our findings suggest that in man, as previously reported in the rat, the lingual serous glands secrete a lipase that acts in the stomach where it initiates the digestion of dietary fat.     

Ultrastructural changes of posterior lingual glands after hypoglossal denervation in hamsters

Posterior lingual glands consist of two sets of minor salivary glands that serve important functions in oral physiology. To investigate the hypothesis that the hypoglossal nerve provides sympathetic innervation to the posterior lingual glands, we examined ultrastructural changes in the glands following hypoglossal denervation. In the posterior deep lingual glands (of von Ebner), the serous acinar cells showed a decrease in the number of secretory granules and an increase in lipofuscin accumulation. The ratios of cells containing lipofuscin granules were 11.39, 36.49 and 50.46%, respectively, of the control, 3- and 7-day post-axotomy glands ( P  < 0.001). Intraepithelial phagocytotic activity was increased. The mucous acinar cells in the posterior superficial lingual glands (of Weber) also showed degenerative changes after hypoglossal denervation. One week after nerve transection, marked cytoplasmic vacuolation and fragmentation of organelles were frequently observed. Degenerative changes were also found in unmyelinated axons associated with the glands. We provide the first evidence of the structural and functional connections between the sympathetic component of the hypoglossal nerve and posterior lingual glands.     

Ultrastructure and histochemistry of human anterior lingual salivary glands (glands of blandin and nuhn)

Background: Speciamens of human anterior lingual salivary glans obtained by surgery and by dissection of cadavers were studied ultrastructurally and histochemically. Methods: Specimens were obtained by surgery for ultrastructural study. Other specimens for histochemistry were obtained by dissection of fresh cadavers. Tissues for electron microscopy were fixed and processed by conventional mesns. Formalin-fixed cadaver specimens were subjected to a battery of tests for glycoconjugates. Results: The anterior lingual salivary glands are composed predominantly of mucous tubules (which come in two distinct sizes: large and small), seromucous demilunes, and rare seromucous acini. Regardless of tubule size, mucous cells are typically in appearance and, like mucous cells in other human salivary glands, contain filamentous bodies. Histochemically, the larger tubules contain neutral glycoproteins, low concentrations of sialoglycoproteins, and large amounts of sulfated glycoproteins. The small mucous tubules contain neutral glycoproteins, much sialoglycoprotein, and relatively small amounts of sulfated glycoprotein. The seromucous cells, whether demilunar or acinar, are identical. They contain numerous secretory granules, which show a spectrum of internal patterns from one individual to another. These cells have considerable concentrations of neutral- and sialoglycoproteins and lower concentrations of sulfated gly-coproteins. Countrary to previously published reports, we could find no differences in the ratio of mucous to seromucous cells along the anteriorposterior lingual axis: there was no gradient of seromucous cells in our specimens. The ducts in the anterior lingual salivary glands are not precise counterparts of those in the major salivary glands, since the former have no capsules, hence lack lobulation. Without these familiar structural landmarks, the only duct that can be identified with certainty is the intercalated duct, and then only if it is in continuity with or lies close to a secretory endpiece. Such ducts consist of simple cuboidal epithelium of prosaic appearance. The ductular epithelium gradually thickens and gives rise to what appear to be excretory ducts consisting of columnar cells with few mitochondria. Scattered within the walls of the walls of the larger ducts are patches of typical striated ducts wherein the taller cells display basal striations resulting from highly folded basal plasma membranes and numerous, vertically oriented, virgulate mitochondria. In other atypical regions of the excretory duct, basal cells may have a primary cilium that juts into the intercellular space. Conclusions: There is a high degree of structural variability in human anterior lingual salivary glands. Because of the technical difficulties in collecting pristine saliva from these glands, the precise functions(s) of these organs remains unknown. © 1994 Wiley-Liss, Inc.     

Fine structure of oncocytes in human salivary glands

Summary Oncocytes, cells displaying marked cytoplasmic acidophilia and granularity, are present in the acini and ducts of normal human salivary glands. These cells apparently originate by a process of sequential transformation of normal epithelial cells. In the early forms, there is a great increase in the number of mitochondria, which are typical in morphology. In later oncocytes, these organelles undergo striking changes in form and size. These mitochondrial changes are accompanied by the gradual disappearance from the oncocyte of other cytoplasmic membrane systems and of plasmalemmar specializations. It is suggested that the structurally modified mitochondria are biochemically deficient.

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Die Feinstruktur der Onkocyten in Speicheldrüsen der Menschen

Zusammenfassung Onkocyten finden sich sowohl in den Acini wie in den Ausführungsgängen normaler Speicheldrüsen. Sie besitzen ein eosinophil granuliertes Cytoplasma und sind wahrscheinlich Abkömmlinge normaler Drüsenzellen, aus denen sie sich über eine Reihe von Zwischenstufen entwickeln. Die Frühformen zeigen eine starke Zunahme der Mitochondrien. In den späten Stadien erfahren die Mitochondrien charakteristische Veränderungen in bezug auf Form und Größe, begleitet von einem Schwund der cytoplasmatischen Membransysteme und weiterer plasmacellulärer Spezialorganellen. Die geschädigten Mitochondrien dürften auch in ihrer biochemischen Leistung beeinträchtigt sein.

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The author acknowledges the expert technical assistance of Mr.Roy R. keppie and Mrs.Mona Brandreth.

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This work was supported in part by grants from the Max C. Fleischmann Foundation of Nevada and the Henry Spenadel Trust, and by N. C. I. grant CA 08748.     

Fine structure of the dorsal lingual epithelium of the lizard,Gekko japonicus (Lacertilia,Gekkonidae)

Three different types of lingual papilla were observed by scanning electron microscopy on the dorsal lingual epithelium of the lizard Gekko japonicus. Dome-shaped lingual papillae were located at the apex. Flat, fan-shaped lingual papillae were seen in the widest area of the lingual body. Long, scale-like lingual papillae were arranged on the latero-posterior dorsal surface. At higher magnification, microvilli and microridges were seen to be widely distributed over the surface of the papillae. By light microscopy, the epithelium of the dome-shaped papillae was composed of single, columnar epithelial cells filled with secretory granules. The tip of the epithelium of the fan-shaped and scale-like papillae was composed of stratified squamous epithelial cells without granules. The major part of the epithelium of these two types of papilla, except the tip area, was also composed of single, columnar epithelial cells with secretory granules. By transmission electron microscopy, a nucleus without a defined shape was seen to be located in the basal part of each of the single, columnar epithelial cells. Rough-surfaced endoplasmic reticulum and Golgi apparatus were well developed around the nucleus. The other, major part of the cytoplasm was filled with the spherical secretory granules, a large number of which had very electron-dense cores and moderately electron-dense peripheral regions. In the stratified squamous epithelium, a nucleus, which tended to be condensed on the free-surface side, was located in the center of each cell. Mitochondria, endoplasmic reticulum, and vesicles were observed in the cytoplasm.     

Fine structure of excretory ducts of human salivary glands

Excretory ducts of human major salivary glands are lined by an epithelium consisting of principal cells and by a discontinuous row of basal cells. The principal cells are tall and columnar with mitochondria, large lipofuscin granules and a central nucleus. Just beneath the plasmalemma bordering the lumen, their cytoplasm contains a number of small granules and vesicles similar to those observed in cells of striated ducts. Both in TEM and SEM, these cells also show large apical protrusions devoid of cytoplasmic organelles that may represent a kind of apocrine secretion. The cytoarchitecture of the principal cells seems to be at variance with that of cells of striated ducts. First, the cell body remains unique and does not split into major basal processes. Second, these cells usually lack the long laminated basal folds, housing vertically aligned mitochondria, that are typical of striated ducts. Instead, below the smooth area occupied by the junctional complexes, the lateral cell surfaces are completely covered by a great number of short irregular processes. These organelle-free folds are apparently involved in the mechanism of ion transport since, at their level, there is a strong reactivity for the transporting enzyme K(+)-pNPPase. The basal cells, which are small and cuboidal, have a dense and filamentous cytoplasm. Their functional role is still uncertain.     

Fine structure of the oxynticopeptic cell in the gastric glands of an elasmobranch species (Halaelurus chilensis)

Gastric mucosa of an elasmobranch species was examined by electron microscope. The gastric glands contain one form of cell whose fine structure is similar to the cell that secretes both hydrochloric acid and pepsinogen of the amphibian gastric glands proper. These oxynticopeptic cells are characterized by: (a) a luminal surface with long projections of cytoplasm having dilatations in their thickness; (b) a tubulo-vesicular system in the apical cytoplasm; (c) a great number of mitochondria, some of which are of great length; (d) a well developed granular endoplasmic reticulum and a conspicuous Golgi apparatus; and (e) a large nucleus with a conspicuous nucleolus. A fourth part of the cells are binucleated. Physiological implications of some of these ultrastructural features are discussed.     

Mouse uterine glands during the peri-implantation period: Fine structure

Mouse uterine glands, obtained during the peri-implantation period of pregnancy, were investigated using light and electron microscopy. From day 4 to day 6 of pregnancy, there was a progressive luminal dilation and an accumulation of dense homogeneous material in the gland lumina. Although numerous large electron-lucent vesicles were present in the apical portion of the glandular cells on day 4, their number decreased by days 5 and 6 of pregnancy. Dense granules were present along the apical border of many glandular cells on day 6. In addition, there was an increase in the number and more orderly arrangement of RER cisternae by day 6 of pregnancy. Cytochemical studies on days 4, 5, and 6 of pregnancy, using the periodic acid-thiocarbohydrazide-silver proteinate method for the ultrastructural localization of carbohydrate material, showed specific staining of the multivesicular bodies and the saccules of the concave surface of the Golgi complex, but not the dilated saccules of the convex surface. Specific staining was also observed over both the luminal material and apical granules present on day 6 of pregnancy. The cytochemical evidence suggests that the secretory product of the uterine glands has carbohydrate components and that carbohydrate material accumulates in the Golgi complex. In addition, the morphological changes observed imply increased secretory activity of the uterine glands during the peri-implantation period. Thus, the uterine glands must be considered an important source of uterine fluid components during the peri-implantation period.     

Fine structure of the differentiating acini in submandibular glands of isoproterenoltreted rats

Chronic treatment with isoproterenol, a β-adrenergic drug, accelerates the postnatal differentiation of the rat submandibular gland. This report compares the ultrastructure of submandibular glands of acute and chronically treated, 2, 11 and 17-day-old rats with that of controls. In all cases a greater number of acinar cells were found in the treated glands. The correlation noted between changes in the nature of the contents of the condensing vaculoes and Golgi apparatus of some proacinar cells and the formation of secretory granules intermediate in appearance between those of proacinar and acinar cells, support the hypothesis that proacinar cells are the precursors of acinar cells in the young rat. Differences in the morphology of secretory granules in acinar cells of treated and control animals are described. It is concluded that precocious differentiation of the submandibular gland may be induced by the administration of isoproterenol as early as the first day of postnatal life, that proacinar cells become recognized as acinar cells following a change in the nature of their secretory product, and that the secretory material produced by acinar cells in the treated animals is not identical to that of the controls.     

Fine structure of the dorsal lingual epithelium of the Japanese lizard, Takydromus tachydromoides.

The histology and the ultrastructure of the dorsal lingual epithelium of the Japanese lizard, Takydromus tachydromoides, were investigated by light and transmission electron microscopy. The epithelium of the anterior and middle portions of the tongue showed "orthokeratinization," being composed of a thick layer of keratinized cells. The epithelium of the posterior portion of the tongue showed "parakeratinization" and "nonkeratinization." Most of the nonkeratinized cells contained large numbers of secretory granules.