Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-26T14:11:10.470Z Has data issue: false hasContentIssue false

Nasal mast cells: a preliminary report on their ultrastructure

Published online by Cambridge University Press:  09 November 2023

A. B. Drake-Lee*
Affiliation:
Royal United Hospital, Bath. The Institute of Laryngology and Otology, London
J. M. Price
Affiliation:
Royal United Hospital, Bath
C. M. Milford
Affiliation:
Royal National Throat Nose and Ear Hospital. London
R. C. Bickerton
Affiliation:
Royal National Throat Nose and Ear Hospital. London
*
Address for correspondence: A. B. Drake-Lee, Royal United Hospital, Combe Park, Bath.
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The ultrastructure of mast cells found in normal inferior turbinate was compared with the features found in the inferior turbinate in two groups of patients, those with allergic rhinitis due to dust mite hypersensitivity and those with nasal polyps; the latter group also had their polyps studied. Adenoid tissue was examined in children with secretory otitis media to see if there was evidence of mast cell degranulation, which would support the hypothesis that either local allergic or other mast cell-mediated reactions caused the condition.

The mast cells from five normal turbinates varied considerably in size, shape and distribution, but were found mainly in the submucosa. There was no difference in the morphology of cells of different sizes and they could not be sub-grouped into either connective tissue or mucosal mast cells. Most. granules were electron dense and homogeneous, although scrolls and crystalline structures were seen occasionally. Some of the granules contained lighter material and others had become vacuoles. Mitochondria were present in all cells suggesting active metabolism.

The three patients with allergic rhinitis showed extensive but variable degranulation of the mast cells in all depths of the mucosa. Nine of the 10 cases with nasal polyps had mast cells identified in both the polyp and the turbinate. They were only normal in one turbinate and in one patient it was impossible to identify mast cells. All the mast cells were degranulated extensively in all other specimens.

The adenoids from seven children had identifiable mast cells, which were less frequently found than in the turbinates. There was some degranulation in four of the patients and in one it was fairly extensive.

Type
Research Article
Copyright
Copyright © JLO (1984) Limited 1987

Footnotes

*

Based on a Prize Essay awarded to Mr. Drake-Lee by Xomed.

References

Behrent, H., Rosenkranz, U., and Schmutzer, W. (1978) Ultrastructure of isolated human mast cells during histamine release with Ionophore A23187. International Archives of Allergy and Applied Immunology, 56: 188-192.CrossRefGoogle Scholar
Bienenstock, J., Befus, D., Pearce, R., Denburg, J., and Goodacre, R. (1982) Mast cell heterogeneity: derivation and function with emphasis on the intestine. Journal of Allergy and Clinical Immunology 70: 407-412.CrossRefGoogle ScholarPubMed
Busutill, A., More, I., and McSeveney, D. (1976) Ultrastructure of the stroma of nasal polyps. Archives of Otolaryngology, 102: 589-595.CrossRefGoogle Scholar
Caulfield, J., Lewis, R., Hein, A., and Austin, K. (1980) Secretions in dissociated human pulmonary mast cells. Journal of Cell Biology, 85: 299-311.CrossRefGoogle ScholarPubMed
Cauna, N., Hindover, K., Manzethi, G., and Swanson, E. (1972) Fine structure of nasal polyps. Annak of Otolaryngology, 81: 41-58.Google ScholarPubMed
Collins, M., Church, M., Bakhshi, K., and Osbourne, J. (1985) Adenoid histamine and its possible relationship to secretory otitis media. Journal of Laryngology and Otology, 99: 685-691.CrossRefGoogle ScholarPubMed
Czarnetzki, B., Figdor, C., Kolde, C., Vroom, T., Aalberse, R., and De Vries, J. (1984) Development of human connective tissue mast cells from purified blood monocytes. Immunology, 51: 549-554.Google ScholarPubMed
Dees, S., and Lefkowitz, D. (1972) Secretory otitis media in allergic children. American Journal of Diseases of Childhood, 124: 364-368.Google ScholarPubMed
Drake-Lee, A., Lowe, D., Swanston, A., and Grace, A. (1984a) Clinical profile and recurrence of nasal polyps. Journal of Laryngology and Otology, 98: 783-793.CrossRefGoogle ScholarPubMed
Drake-Lee, A., Barker, T., and Thurley, K. (1984b) Nasal polyps (2) Fine structure of mast cells. Journal of Laryngology and Otology, 98: 285-292.CrossRefGoogle Scholar
Dvorak, A., Galli, S., Schulman, E., Lichtenstein, L., and Dvorak, H. (1983) Basophils and mast cell degranulation: ultrastructural analysis of mechanisms of mediator release. Federal Proceedings, 42: 2510-2515.Google ScholarPubMed
Enerback, L. (1981) The gut mucosal mast cells. Monographs of Allergy, 17: 222-232.Google Scholar
Galli, S., Dvorak, A., and Dvorak, H. (1984) In Progress in Allergy, Vol. 34. Mast Cell Activation and Mediator Release. Ed. Ishizaka, K. Chapter 1. Basophils and mast cells: morphological insights into their biology, secretory patterns and function. Karger. Basel.Google Scholar
Hibbert, J., and Stell, P. (1982) The role of enlarged adenoids in the aetiology of serous otitis media. Clinical Otolaryngology, 7: 253-256.CrossRefGoogle ScholarPubMed
Ishizaka, K., and Ishizaka, T. (1967) Identification of IgE antibodies as a carrier of reaginic activity. Journal of Immunology, 99: 1187-2298.CrossRefGoogle Scholar
Kawabori, S., Okuda, M., and Unno, T. (1983) Mast cells in allergic nasal epithelium and lamina propria before and after provocation. Clinical Allergy, 13: 181-189.CrossRefGoogle ScholarPubMed
Kessler, S., and Kuhn, C. (1975) Scanning electron microscopy of mast cell degranulation. Laboratory Investigations, 32: 71-77.Google ScholarPubMed
Maw, A. R. (1983) Chronic otitis media with effusion (glue ear) and adenoidectomy: prospective randomised controlled study. British Medical Journal, ii: 1586-1588.CrossRefGoogle Scholar
Miller, H. (1980) The structure, origin and function of mucosal mast cells. A brief review. Biologica Cellulaire, 39: 229-232.Google Scholar
Okuda, M., Ohtsuka, H., and Kawabori, S. (1983) Basophil leukocytes and mast cells in the nose. European Journal of Respiratory Diseases, 64 (Supplement 128): 7-14.Google Scholar
Reynolds, E. S. (1963) The use of lead citrate at high pH as an electron opaque stain in electron microscopy. Journal of Cell Biology, 17: 208-213.CrossRefGoogle ScholarPubMed
Spurr, A. (1969) A low viscosity epoxy resin medium for electron microscopy. Journal of Ultastructural Research, 26: 31-43.CrossRefGoogle ScholarPubMed
Strobel, S., Miller, H., and Ferguson, A. (1981) Human intestinal mast cells: evaluation of fixation and staining techniques. Journal of Clinical Pathology, 34: 851-858.CrossRefGoogle ScholarPubMed
Trotter, C., and Orr, T. (1973) A fine structure study of some cellular components in allergic reactions. Clinical Allergy, 3: 411-425.CrossRefGoogle ScholarPubMed
Wihl, J. (1979) Mast cells in the nasal mucosa. In The Mast Cell: its role in health and disease. Eds. Pepys, J., Edwards, A. Pitman Press, Bath, pp. 758-756.Google Scholar