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The Journal of Biophysical and Biochemical Cytology logoLink to The Journal of Biophysical and Biochemical Cytology
. 1961 May 1;10(1):47–57. doi: 10.1083/jcb.10.1.47

ELECTRON MICROSCOPY OF THE OXYNTIC CELL IN THE GASTRIC GLANDS OF THE BULLFROG, RANA CATESBIANA

II. The Acid-Secreting Gastric Mucosa

Albert W Sedar 1
PMCID: PMC2225058  PMID: 13749582

Abstract

The oxyntic cell in the gastric glands of the bullfrog was examined in lead hydroxide-stained sections of gastric mucosae fixed in buffered osmium tetroxide and embedded in n-butyl methacrylate. During gastric acid secretion (pH 1–2) induced by histamine administration in cannulated frogs, the pattern of fine structure in the oxyntic cell differs strikingly from that in the oxyntic cell of the non-acid-secreting stomach. The relative number of smooth surfaced profiles decreases and a greater concentration of these elements is associated with the apical region of the oxyntic cell facing the lumen of the gastric gland. Similar concentrations of these elements are found in those regions of cytoplasm surrounding intercellular canaliculi which lie between adjacent cells and communicate with the lumen of a gastric gland. In these regions, the smooth surfaced profiles (35 to 65 mµ in width) characteristically form a tubular network. The membrane-bounded contents appear to be continuous with the extracellular medium, both on the capillary side and at the apical surface of the cell adjoining the lumen of the gastric gland. Mitochondria are distributed randomly in the cytoplasmic matrix of the oxyntic cell.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BRADFORD N. M., DAVIES R. E. The site of hydrochloric acid production in the stomach as determined by indicators. Biochem J. 1950 Apr;46(4):414–420. doi: 10.1042/bj0460414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. HOGBEN C. A. Physiochemical aspects of hydrochloric acid formation. Am J Dig Dis. 1959 Mar;4(3):184–193. doi: 10.1007/BF02231222. [DOI] [PubMed] [Google Scholar]
  3. VIAL J. D., ORREGO H. Electron microscope observations on the fine structure of parietal cells. J Biophys Biochem Cytol. 1960 Apr;7:367–372. doi: 10.1083/jcb.7.2.367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. WATSON M. L. Reduction of heating artifacts in thin sections examined in the electron microscope. J Biophys Biochem Cytol. 1957 Nov 25;3(6):1017–1022. doi: 10.1083/jcb.3.6.1017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. II. Application of solutions containing lead and barium. J Biophys Biochem Cytol. 1958 Nov 25;4(6):727–730. doi: 10.1083/jcb.4.6.727. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. WATSON M. L. The use of carbon films to support tissue sections for electron microscopy. J Biophys Biochem Cytol. 1955 Mar;1(2):183–184. doi: 10.1083/jcb.1.2.183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. WHITE T. D., SWIGART R. H., REHM W. S. Limitations of the use of indicators for determination of acidity in the gastric lumina. Am J Physiol. 1956 Mar;184(3):453–456. doi: 10.1152/ajplegacy.1956.184.3.453. [DOI] [PubMed] [Google Scholar]

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