Skip to main content
Log in

Ultrastructure of the main excretory duct epithelium of the female mouse submandibular gland with special reference to sexual dimorphism

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Abstract

The fine structure of the main excretory duct epithelium (MEDE) of female mouse submandibular gland was investigated by scanning and transmission electron microscopy and the results compared with the previously established structure of male mouse MEDE. A comparative analysis of the subepithelial capillaries of both sexes was also performed. In this pseudostratified epithelium, principal cell-types were observed: types-I,-II,-III and basal cells. This differed significantly from male MEDE, where type-II and-III are absent and type-I cells are the most numerous. The latter cell-type had abundant mitochondria, a few lipid-containing granules, lysosomes in the infra-nuclear cytoplasm and well-developed basal infoldings. These cells were also characterized by abundant glycogen granules throughout the cytoplasm, many profiles of strands of smooth endoplasmic reticulum in the apical region, and lysosomes in the infra-nuclear region. Type-II cells were the second most numerous. Their most characteristic features were the presence of tubular vesicles which appeared to be invaginated from the plasma membrane, RER, SER, free ribosomes, a few peroxisomes with nucleoids, and primary lysosomes in extremely light cytoplasm. They had many mitochondria throughout the cytoplasm, except in the apical region, a few lipid-containing granules and no basal infoldings. Type-III cells were very few and were characterized by well developed basal infoldings, abundant free ribosomes, RER, SER, vesicles containing moderately dense material, and many lipid-containing granules. They also had many mitochondria throughout the cytoplasm, except apically. Basal cells had a large nucleus and the cytoplasm had few organelles. In the male continuous capillaries predominated in the subepithelial network, and capillary density per 200 μm of epithelium (3.76±1.54) was lower than in the female, as was the number of fenestrae per 10 μm of available endothelium (4.46±1.71). In the female, fenestrated capillaries predominated, and the capillary density per 200 μm of epithelium was 6.76 (±1.54), and the number of fenestrae per 10 μm of available endothelium was 4.91 (±1.77).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Angeletti PU, Salvi ML, Tacckini G (1964) Inhibition of the testosterone effect on the submaxillary gland by actiomycin-D. Experientia 20:612–613

    Google Scholar 

  • Borst P (1986) How proteins get into microbodies (peroxisomes, glyoxysomes, glycosomes). Biochim Biophys Acta 866:179–203

    Google Scholar 

  • Burgen ASV, Seeman P (1958) The role of the salivary duct system in the formation of the saliva. Can J Biochem Physiol 36:119–143

    Google Scholar 

  • Caramia F (1966) Ultrastructure of mouse submaxillary gland. I. Sexual differences. J Ultrastruct Res 16:505–523

    Google Scholar 

  • Clough G, Smaje LH (1984) Exchange area and surface properties of the microvasculature of the rabbit submandibular gland following duct ligation. J Physiol 354:445–456

    Google Scholar 

  • Duve C de, Baudhuin P (1966) Peroxisomes. Physiol Reviews 46:323–357

    Google Scholar 

  • Fekete E (1941) Histology. In: Snell GD (ed) The biology of the laboratory mouse. Blakiston, Philadelphia, pp 89–167

    Google Scholar 

  • Fujita M, Yamamoto T (1984) Selective demonstration by tannic acid of a special cytoplasmic tubular system in the chloride cells of teleost gills. Arch Histol Jpn 47:113–118

    Google Scholar 

  • Gresik EW (1966) A previously unreported cell type in female mouse submandibular glands. J Cell Biol 31:144A

    Google Scholar 

  • Gresik EW, MacRae EK (1975) The postnatal development of the sexually dimorphic duct system and of amylase activity in the submandibular glands of mice. Cell Tissue Res 157:411–422

    Google Scholar 

  • Hand AR (1973) Morphologic and cytochemical identification of peroxisomes in the rat parotid and other exocrine gland. J Histochem Cytochem 21:131–141

    Google Scholar 

  • Henderson JR, Moss MC (1985) A morphometric study of the endocrine and exocrine capillaries of the pancreas. Q J Exp Physiol 70:347–356

    Google Scholar 

  • Hosoi K, Kobayashi M, Hiramatsu N, Minami N, Ueha T (1979) Androgenic regulation of N-acetyl-glucosaminidase activity in the submaxillary gland of mice. J Biochem 85:1483–1488

    Google Scholar 

  • Hruban Z, Rechcigl M (1969) Microbodies and related particles: Microbodies of various animal species. Int Rev Cytol [Suppl] 1:20–59

    Google Scholar 

  • Karnaky KJ Jr, Ernst SA, Philpott CW (1976a) Teleost chloride cell. I. Response of pupfish Cyprinodom variegatus gill Na, K-ATPase and chloride cell fine structure to various high salinity environments. J Cell Biol 70:144–156

    Google Scholar 

  • Karnaky KJ Jr, Kinter LB, Kinter WB, Stirling CE (1976b) Teleost chloride cell. II. Autoradiographic localization of gill Na, K-ATPase in killifish Fundulus heteroclitus adapted to low and high salinity environments. J Cell Biol 70:157–177

    Google Scholar 

  • Karnovsky MJ (1967) The ultrastructural basis of capillary permeability studied with peroxidase as a tracer. J Cell Biol 35:213–236

    Google Scholar 

  • Karnovsky MJ (1971) Use of ferrocyanide-reduced osmium tetroxide in electron microscopy. 14th Annual Meeting Am Soc Cell Biol, p 146

  • Kindl H (1982) The biosynthesis of microbodies (Peroxisomes, Glyoxysomes). Int Rev Cytol 80:193–229

    Google Scholar 

  • Komuro T, Yamamoto T (1975) The renal chloride cell of the fresh-water catfish, Parasilurus asotus, with special reference to the tubular membrane system. Cell Tissue Res 160:263–271

    Google Scholar 

  • Lacassagne A (1940) Dimorphism sexuel de la glande sousmaxillaire chez la souris. CR Soc Biol 133:180–181

    Google Scholar 

  • Lazarow PB, Duve C de (1976) A fatty acyl-CoA oxidizing system in rat liver peroxisomes; enhancement by clofibrate, a hypolipidemic drug. Proc Natl Acad Sci USA 73:2043–2046

    Google Scholar 

  • Mizuhira V, Amakawa T, Yamashina S, Shirai N, Uchida S (1970) Electron microscopic studies on the localization of sodium ions and sodium-potassium-activated adenosinetriphosphatase in chloride cells of eel gills. Exp Cell Res 59:346–348

    Google Scholar 

  • Nakamura T, Fujji M, Kaiho M, Kumegawa M (1974) Sex difference in glucose-6-phosphate dehydrogenase activity in the submaxillary gland of mice. Biochim Biophys Acta 362:110–120

    Google Scholar 

  • Napolitano L, Lebaron F, Scaletti J (1967) Preservation of myelin lamellar structure in the absence of lipids. J Cell Biol 34:817–826

    Google Scholar 

  • Oliver WJ, Gross F (1967) Effect of testosterone and duct ligation on submaxillary renin-like principle. Am J Physiol 213:341–346

    Google Scholar 

  • Sato A, Miyoshi S (1988) Ultrastructure of the main excretory duct of the rat parotid and submandibular glands with a review of the literature. Anat Rec 220:239–251

    Google Scholar 

  • Sato A, Miyoshi S (1990) Morphometric study of the microvasculature of the main excretory duct subepithelia of the rat parotid. submandibular and sublingual salivary glands. Anat Rec 226:288–294

    Google Scholar 

  • Sato A, Miyoshi S (1992) Occurrence of unusual heterogeneous lipid-containing granule storing cells in the main excretory duct epithelium of the male mouse submandibular gland. Cell Tissue Res 268:31–40

    Google Scholar 

  • Sawada K, Noumura T (1991) Effects of castration and sex steroids on sexually dimorphic development of the mouse submandibular gland. Acta Anat 140:97–103

    Google Scholar 

  • Schneyer LH (1968) Secretory processes in perfused excretory duct of rat submaxillary gland. Am J Physiol 215:664–670

    Google Scholar 

  • Schneyer LH (1969) Secretion of potassium by perfused excretory duct of rat submaxillary gland. Am J Physiol 217:1324–1329

    Google Scholar 

  • Schneyer LH, Young JA, Schneyer CA (1972) Salivary secretion of electrolytes. Physiol Rev 52:720–777

    Google Scholar 

  • Shirai N, Utida S (1970) Development and degeneration of the chloride cells during seawater and freshwater adaptation of the Japanese eel, Anguilla japonica. Z Zellforsch 103:247–264

    Google Scholar 

  • Simionescu N, Simionescu M, Palade GE (1973) Permeability of muscle capillaries to exogenous myoglobin. J Cell Biol 57:424–452

    Google Scholar 

  • Young JA, Frömter E, Schögel E, Hamann KF (1967) A microperfusion investigation of sodium resorption and potassium secretion by the main excretory duct of the submaxillary gland. Pflüger Arch Ges Physiol 295:157–172

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sato, A., Goto, F. & Miyoshi, S. Ultrastructure of the main excretory duct epithelium of the female mouse submandibular gland with special reference to sexual dimorphism. Cell Tissue Res 277, 407–415 (1994). https://doi.org/10.1007/BF00300213

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00300213

Key words

Navigation