Literature DB >> 3429300

Ultrastructure of the angularis oris salivary gland in the house sparrow.

T Nagato1, B Tandler.   

Abstract

The angularis oris gland, an avian salivary gland that lies beneath the zygomatic arch, was studied in the house sparrow by means of light and electron microscopy. The gland consists of lobules composed of epithelial tubules and folds on a delicate connective tissue framework. The lobules are drained by large channels to form an intraglandular duct, which becomes the main extraglandular duct. The tubules, folds, and all ducts are covered by pseudostratified epithelium that shows progressive changes from the blind ends of tubules to the duct system. At the closed end of the tubules, the tall cells contain an aggregation of closely packed mucous droplets; their mitochondria are long and slender. As the epithelium nears the duct system, the mucus content of the tall cells is reduced and the mitochondria, which are increased in number, are ovoid. The lateral borders of the cells are complexly interlocked. In the ducts, mitochondria-rich cells with extensive lateral interfoliation comprise the major cell type; some of these cells contain a few mucous droplets at their apices. The basal cells of the pseudostratified epithelium have the same basic structure regardless of their location. These pyramidal cells have abundant cytofilaments and are joined to the basal lamina by many hemidesmosomes. Despite the absence of clear-cut morphological zonation, the angularis oris may function in a manner that is analogous to mammalian salivary glands: secretory cells produce the organic component of the saliva, mucus, while the mitochondria-rich cells with their extensive lateral membranes probably resorb electrolytes to render the final saliva hypotonic.

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Mesh:

Year:  1986        PMID: 3429300      PMCID: PMC1166500     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  13 in total

1.  THE POISON GLAND OF THE COTTONMOUTH MOCCASIN, ANCISTRODON P. PISCIVORUS, AS OBSERVED WITH THE ELECTRON MICROSCOPE.

Authors:  D L ODOR
Journal:  J Morphol       Date:  1965-07       Impact factor: 1.804

2.  Epon-maraglas embedment for electron microscopy.

Authors:  B Tandler; R J Walter
Journal:  Stain Technol       Date:  1977-07

Review 3.  Salivary secretion of electrolytes.

Authors:  L H Schneyer; J A Young; C A Schneyer
Journal:  Physiol Rev       Date:  1972-07       Impact factor: 37.312

4.  Evidence for amylase in avian salivary glands.

Authors:  S A Jerrett; W R Goodge
Journal:  J Morphol       Date:  1973-01       Impact factor: 1.804

5.  Fine structure of the venom gland epithelium of the South American rattlesnake and radioautographic studies of protein formation by the secretory cells.

Authors:  H Warshawsky; A Haddad; R P Goncalves; V Valeri; F L De Lucca
Journal:  Am J Anat       Date:  1973-09

Review 6.  Salivary glands of snakes.

Authors:  E Kochva; C Gans
Journal:  Clin Toxicol       Date:  1970-09       Impact factor: 4.467

7.  Fine structure of Duvernoy's gland of the Japanese colubrid snake, Rhabdophis tigrinus.

Authors:  S Yoshie; M Ishiyama; T Ogawa
Journal:  Arch Histol Jpn       Date:  1982-09

8.  A histological and histochemical study of the development of salivary glands in the chick (Gallus domesticus).

Authors:  L Shih; M A Gibson
Journal:  Can J Zool       Date:  1967-09       Impact factor: 1.597

9.  AN IMPROVED STAINING METHOD FOR ELECTRON MICROSCOPY.

Authors:  J G STEMPAK; R T WARD
Journal:  J Cell Biol       Date:  1964-09       Impact factor: 10.539

10.  The fine structure of the gastric mucosa in the bat.

Authors:  S ITO; R J WINCHESTER
Journal:  J Cell Biol       Date:  1963-03       Impact factor: 10.539

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