Skip to main content
British Journal of Experimental Pathology logoLink to British Journal of Experimental Pathology
. 1986 Dec;67(6):821–829.

Development of the airway epithelium and submucosal glands in the pig lung: changes in epithelial glycoprotein profiles.

A N Mills, M T Lopez-Vidriero, S G Haworth
PMCID: PMC2013126  PMID: 3801296

Abstract

Glycoproteins in the normal airway surface epithelium and submucosal glands of 13 Large White pigs were studied from birth to adult life using alcian blue (AB) staining at pH 2.6 or at pH 1.0, with and without sialidase digestion, and by the combination of AB and PAS (AB/PAS) stains. Immediately after birth the percentage of cells producing acidic and neutral glycoproteins increased in both airway surface epithelium and submucosal glands. In the airway surface epithelium, the percentage of mucus-secreting cells producing sulphated glycoprotein increased with age, whereas in the submucosal glands the glycoproteins were mainly sulfated between birth and 3 days and sialylated between 3 days and adult life. The percentage of cells producing neutral glycoprotein in the airway surface epithelium increased during the first 24 h of life after which there was little change with age. In the submucosal glands, however, the greatest increase in the percentage of cells producing neutral glycoprotein occurred between 7 days and adult life. The rapid increase of intracellular glycoprotein production at birth and the presence of the same types of glycoprotein in the immature pig and mature human lung, suggest that the pig may be a useful model in which to study mechanisms and changes of glycoprotein synthesis and secretion during lung development.

Full text

PDF
821

Selected References

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

  1. Boat T. F., Cheng P. W., Iyer R. N., Carlson D. M., Polony I. Human respiratory tract secretion. Mucous glycoproteins of nonpurulent tracheobronchial secretions, and sputum of patients with bronchitis and cystic fibrosis. Arch Biochem Biophys. 1976 Nov;177(1):95–104. doi: 10.1016/0003-9861(76)90419-7. [DOI] [PubMed] [Google Scholar]
  2. Haworth S. G., Hislop A. A. Adaptation of the pulmonary circulation to extra-uterine life in the pig and its relevance to the human infant. Cardiovasc Res. 1981 Feb;15(2):108–119. doi: 10.1093/cvr/15.2.108. [DOI] [PubMed] [Google Scholar]
  3. Jones R., Bolduc P., Reid L. Goblet cell glycoprotein and tracheal gland hypertrophy in rat airways: the effect of tobacco smoke with or without the anti-inflammatory agent phenylmethyloxadiazole. Br J Exp Pathol. 1973 Apr;54(2):229–239. [PMC free article] [PubMed] [Google Scholar]
  4. Jones R., Reid L. Secretory cell hyperplasia and modification of intracellular glycoprotein in rat airways induced by short periods of exposure to tobacco smoke, and the effect of the antiinflammatory agent phenylmethyloxadiazole. Lab Invest. 1978 Jul;39(1):41–49. [PubMed] [Google Scholar]
  5. Jones R., Reid L. The effect of pH on Alcian Blue staining of epithelial acid glycoproteins. II. Human bronchial submucosal gland. Histochem J. 1973 Jan;5(1):19–27. doi: 10.1007/BF01012041. [DOI] [PubMed] [Google Scholar]
  6. Lamb D., Reid L. Acidic glycoproteins produced by the mucous cells of the bronchial submucosal glands in the fetus and child: a histochemical autoradiographic study. Br J Dis Chest. 1972 Oct;66(4):248–253. doi: 10.1016/0007-0971(72)90043-5. [DOI] [PubMed] [Google Scholar]
  7. Lamb D., Reid L. Mitotic rates, goblet cell increase and histochemical changes in mucus in rat bronchial epithelium during exposure to sulphur dioxide. J Pathol Bacteriol. 1968 Jul;96(1):97–111. doi: 10.1002/path.1700960111. [DOI] [PubMed] [Google Scholar]
  8. REID L. Measurement of the bronchial mucous gland layer: a diagnostic yardstick in chronic bronchitis. Thorax. 1960 Jun;15:132–141. doi: 10.1136/thx.15.2.132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Sherman J. M., Cheng P. W., Tandler B., Boat T. F. Mucous glycoproteins from cat tracheal goblet cells and mucous glands separated with EDTA. Am Rev Respir Dis. 1981 Oct;124(4):476–479. doi: 10.1164/arrd.1981.124.4.476. [DOI] [PubMed] [Google Scholar]
  10. Stahl G. H., Ellis D. B. Biosynthesis of respiratory-tract mucins. A comparison of canine epithelial goblet-cell and submucosal-gland secretions. Biochem J. 1973 Dec;136(4):845–850. doi: 10.1042/bj1360845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. WARREN L., SPICER S. S. Biochemical and histochemical identification of sialic acid containing mucins of rodent vagina and salivary glands. J Histochem Cytochem. 1961 Jul;9:400–408. doi: 10.1177/9.4.400. [DOI] [PubMed] [Google Scholar]

Articles from British journal of experimental pathology are provided here courtesy of Wiley

RESOURCES