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The influence of fixation on the carbohydrate cytochemistry of rat salivary gland secretory granules

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A series of studies was performed to assess the optimum fixation conditions for staining of carbohydrate-containing constituents of rat salivary gland secretory granules. In the parotid and submandibular salivary glands of the rat, the reactivity of secretory granules, at both the light and electron microscopic level, with routine stains and with cytochemical reagents was highly dependent upon the nature of the fixative employed. At the light microscopic level, secretory granules in rat parotid gland were periodic acid-Schiff (PAS) positive if fixed with buffered formalin fixatives. However, if the gland was fixed with lipid-solvent-containing fixatives, or with formalin at a very acid pH (as in Bouin's fixative), the PAS reactivity of the granules was lost. In the submandibular gland of rats, the acinar cells and granular tubules behaved similarly after such fixation in terms of their PAS reactivity, particularly in males; acinar cells of the female submandibular gland stained only lightly with PAS. At the fine structural level, the morphology of secretory granule constituents depended on the buffer used (cacodylate, phosphate or collidine) and on whether or not tissue was post-osmicated. Post-osmication considerably reduced the reaction of secretory granule components with stains for carbohydrates.

The experimental evidence indicated that the carbohydrate-containing components of both parotid and submandibular gland secretory granules were not typical long-chain neutral or acidic mucins, but were rather glycolipids or lipophilic glycoproteins that were solubilized by lipid solvents or at acidic pH and were lost or destroyed in the presence of strong oxidants.

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References

  • Amsterdam, A., Ohad, I. &Schramm, M. (1969). Dynamic changes in the ultrastructure of the acinar cell of the rat parotid gland during the secretory cycle.J. Cell Biol. 41, 753.

    Google Scholar 

  • Cope, G. H., Pratten, M. K. &Williams, M. A. (1976). Correlative morphological and biochemical study of the effects of isoprenaline on the organelle and membrane content of the rabbit parotid gland.Histochem. J. 8, 403.

    Google Scholar 

  • Dewey, M. (1958). A histochemical and biochemical study of the parotid gland in normal and hypophysectomized rats.Am. J. Anat. 102, 243.

    Google Scholar 

  • Elftman, H. (1958). Effects of fixation on lipoid histochemistry.J. Histochem. Cytochem. 6, 317.

    Google Scholar 

  • Flon, H. &Gerstner, R. (1968). Salivary glands of the hamster. I. The submandibular gland: A histochemical study after preservation with various fixatives.Acta Histochem. 31, 234.

    Google Scholar 

  • Hotchkiss, R. D. (1948). A microchemical reaction resulting in the staining of polysaccharide structures in fixed tissue preparations.Arch. Biochem. 16, 131.

    Google Scholar 

  • Kanda, T., Mayfield, E. D., Jr., &Ghidoni, J. J. (1968). Ultrastructural alterations in submaxillary acinar cells following isproterenol administration: A new form of secretion granules.Expl molec. Pathal. 9, 189.

    Google Scholar 

  • Karnovsky, M. J. (1965). A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron microscopy.J. Cell Biol. 27, 137A.

    Google Scholar 

  • Koenig, H. (1967). On the structure-linked latency of the lysosomal enzymes.J. Histochem. Cytochem. 15, 767–8.

    Google Scholar 

  • Koenig, H. (1969). Lysosomes in the nervous system. In:Lysosomes in Biology and Pathology, Vol. 2. (eds. J. T. Dingle & H. B. Fell) pp. 11–162. Amsterdam: North Holland Publ. Co

    Google Scholar 

  • Kronman, J. &Chauncey, H. (1965). Testosterone-induced changes in salivary gland histochemistry in the female golden hamster.J. oral Therapeutics Pharmacology 1, 392.

    Google Scholar 

  • Kronman, J. &Spinale, J. (1965). A histochemical study of testosterone-induced changes in the submandibular and sublingual gland of mice.Am. J. Anat. 117, 417.

    Google Scholar 

  • Lacassagne, A. (1940). Dimorphisme sexuel de la glande sous-maxillaire chez la souris.C. r. Soc. Biol. (Paris) 133, 180.

    Google Scholar 

  • Leblond, C. P. (1950). Distribution of periodic acid-reactive carbohydrates in the adult rat.Am. J. Anat. 86, 1.

    Google Scholar 

  • Lillie, J. H. &Han, S. S. (1973). Secretory protein synthesis in the stimulated rat parotid gland. Temporal dissociation of the maximal response from secretion.J. Cell. Biol. 59, 708.

    Google Scholar 

  • Lillie, R. D. (1965).Histopathologic Technique and Practical Histochemistry. 3rd edn, p. 198. N.Y.: Blakiston Div., McGraw-Hill Book Co.

    Google Scholar 

  • Munger, B. L. (1964). Histochemical studies on seromucous- and mucous-secreting cells of human salivary glands.Am. J. Anat. 115, 411.

    Google Scholar 

  • Pearse, A. G. E. (1961).Histochemistry. Theoretical and Applied 2nd edn., pp. 232 and 71. Boston: Little Brown and Company.

    Google Scholar 

  • Pizzolato, P. &Lillie, R. D. (1973). Mayer's tannic acid-ferric chloride stain for mucins.J. Histochem. Cytochem. 21, 56.

    Google Scholar 

  • Ravetto, C., Galluzzo, F. &Siervo, R. (1964). On the presence of a ganglioside in bovine submaxillary gland.J. Histochem. Cytochem. 12, 791.

    Google Scholar 

  • Sannes, P. L., Katsuyama, T. & Spicer, S. S. (1977). Tannic acid-metal salt sequences in histochemistry and ultrastructural cytochemistry. (Submitted)

  • Seifert, G. (1962). Electronmikroskopische Befunde an den Speicheldrusenacini nach Enwirkung von Noradrenalin.Beit. Pathol. Anat. 127, 111–36.

    Google Scholar 

  • Seifert, G. (1967). Experimental sialadenosis by isoproterenol and other agents: histochemistry and electron microscopy. In:Secretory Mechanisms of Salivary Glands. (eds. L. H. Schneyer and C. A. Schneyer) pp. 191–207. N.Y.: Academic Press.

    Google Scholar 

  • Shackleford, J., &Klapper, C. E. (1962). A sexual dimorphism of hamster submaxillary mucin.Anat. Rec. 142, 495.

    Google Scholar 

  • Shackleford, J. &Wilborn, W. (1968). Structural and histocyemical diversity in mammalian salivary glands.Alabama J. Med. Sci. 5, 180.

    Google Scholar 

  • Simson, J. A. V. (1969a). A study of the effects of isoproterenol on the cytology of the parotid and submandibular glands of the rat. Ph.D. Thesis, S.U.N.Y., Upstate Medical Center, Syracuse, New York.

    Google Scholar 

  • Simson, J. A. V. (1969b). Discharge and restitution of secretory material in the rat parotid gland in response to isoproterenol.Z. Zellforsch.,101, 175.

    Google Scholar 

  • Simson, J. A. V., Hall, B. J. &Spicer,S. S. (1973). Histochemical evidence for lipoidal material in secretory granules of rat salivary glands.Histochem. J.,5, 239–54.

    Google Scholar 

  • Simson, J. A. V., Spicer, S. S. &Hall, B. J. (1974). Morphology and cytochemistry of rat salivary gland acinar secretory granules and their alteration by isoproterenol I. Parotid gland.J. Ultrastruct. Res. 48, 465–82.

    Google Scholar 

  • Simson, J. A. V., Spicer, S. S. & Sannes, P. L. (1977). Morphology and cytochemistry of rat submandibular acinar cell granules and their alteration by isoproterenol. (Submitted)

  • Spurr, A. R. (1969). A low-viscosity epoxy resin embedding medium for electron microscopy.J. Ultrast. Res. 26, 31.

    Google Scholar 

  • Takahama, M. &Barka, T. (1967). Electron microscopic alterations of submaxillary gland produced by isoproterenol.J. Ultrast. Res. 17, 452.

    Google Scholar 

  • Takaya, K. (1976). The variable refractivity of the protein or polypeptide hormone-producing cells showing a unique luminescence in the dark-field microscope.Histochem. J. 8, 13.

    Google Scholar 

  • Thiery, J. P. (1967). Mise en evidence des polysaccharides sur coupes fines en microscopie electronique.J. Microscopie. 6, 987.

    Google Scholar 

  • Warren, L. &Spicer, S. S. (1961). Biochemical and histochemical identification of sialic acid containing mucous of rodent vagina and salivary glands.J. Histochem. Cytochem. 9, 400.

    Google Scholar 

  • Wigglesworth, B. B. (1971). Bound lipid in the tissues of mammal and insect: a new histochemical method.J. Cell Science 8, 709.

    Google Scholar 

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Simson, J.A.V. The influence of fixation on the carbohydrate cytochemistry of rat salivary gland secretory granules. Histochem J 9, 645–657 (1977). https://doi.org/10.1007/BF01002906

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