Abstract
The distribution and enumeration of mast cell subpopulations within the respiratory tract of a high- and low-Ige responder rat strain was determined during postnatal development. Mast cells were identified in adjacent sections by the alcian blue (AB)/safranin (SAF) staining sequence, or using immunoperoxidase to detect the rat mast cell proteinases I (RMCPI) or II (RMCPII). At birth both mucosal mast cells (MMC) and connective tissue mast cells (CTMC) were represented in very low numbers at distinct locations throughout the respiratory tract. The total number of mast cells increased with age. MMC (AB+/RMCPII+ mast cells) were the predominant phenotype in the epithelium and lamina propria of the trachea and the major conducting airways of the lung in all age groups. In contrast, CTMC (AB+/RPMCPI+ and SAF+/RMCPI+ mast cells) predominated in the submucosa of the trachea and major conducting airways as well as in the parenchyma and visceral pleura of the peripheral lung. Both phenotypes co-exist in similar proportions in peribronchial adventitial tissue and adventitia surrounding large blood vessels in neonates as well as adults. In rats the tracheal epithelium is densely populated by MMC from around the time of weaning (3 weeks) and a small but generalized increase in the number of MMC at all sites within the respiratory tract is noted from this time. This increase in MMC frequency in tissue sections with increasing age is mirrored by the levels of circulating serum RMCPII. The number of bone marrow-derived MMC also increased with increasing age prior to weaning, with a significant drop (P less than 0.01) at 4 weeks of age before returning to the peak numbers in 3-week-old rats. The high-IgE responder Brown Norwegian (BN) rat strain constitutively produces significantly more IgE than the low-IgE responder White albino Glaxo (WAG) strain (P less than 0.001) at all ages studied. In contrast, only minor differences between the number and distribution of mast cells in the two strains were observed.
Full text
PDF






Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bachelet C. M., Bernaudin J. F., Fleury-Feith J. Distribution and histochemical characterization of pulmonary mast cells in the rat and guinea pig. Int Arch Allergy Appl Immunol. 1988;87(3):225–229. doi: 10.1159/000234677. [DOI] [PubMed] [Google Scholar]
- Barrett K. E., Szucs E. F., Metcalfe D. D. Mast cell heterogeneity in higher animals: a comparison of the properties of autologous lung and intestinal mast cells from nonhuman primates. J Immunol. 1986 Sep 15;137(6):2001–2008. [PubMed] [Google Scholar]
- Burri P. H. The postnatal growth of the rat lung. 3. Morphology. Anat Rec. 1974 Sep;180(1):77–98. doi: 10.1002/ar.1091800109. [DOI] [PubMed] [Google Scholar]
- Combs J. W., Lagunoff D., Benditt E. P. Differentiation and proliferation of embryonic mast cells of the rat. J Cell Biol. 1965 Jun;25(3):577–592. doi: 10.1083/jcb.25.3.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Craig S. S., Schechter N. M., Schwartz L. B. Ultrastructural analysis of maturing human T and TC mast cells in situ. Lab Invest. 1989 Jan;60(1):147–157. [PubMed] [Google Scholar]
- Cummins A. G., Munro G. H., Miller H. R., Ferguson A. Association of maturation of the small intestine at weaning with mucosal mast cell activation in the rat. Immunol Cell Biol. 1988 Oct-Dec;66(Pt 5-6):417–422. doi: 10.1038/icb.1988.53. [DOI] [PubMed] [Google Scholar]
- Denburg J. A., Telizyn S., Belda A., Dolovich J., Bienenstock J. Increased numbers of circulating basophil progenitors in atopic patients. J Allergy Clin Immunol. 1985 Sep;76(3):466–472. doi: 10.1016/0091-6749(85)90728-6. [DOI] [PubMed] [Google Scholar]
- Enerbäck L. Mast cells in rat gastrointestinal mucosa. 2. Dye-binding and metachromatic properties. Acta Pathol Microbiol Scand. 1966;66(3):303–312. doi: 10.1111/apm.1966.66.3.303. [DOI] [PubMed] [Google Scholar]
- Enerbäck L. Mucosal mast cells in the rat and in man. Int Arch Allergy Appl Immunol. 1987;82(3-4):249–255. doi: 10.1159/000234199. [DOI] [PubMed] [Google Scholar]
- Enerbäck L., Norrby K. The mast cells. Curr Top Pathol. 1989;79:169–204. doi: 10.1007/978-3-642-73855-5_8. [DOI] [PubMed] [Google Scholar]
- Gibson S., Miller H. R. Mast cell subsets in the rat distinguished immunohistochemically by their content of serine proteinases. Immunology. 1986 May;58(1):101–104. [PMC free article] [PubMed] [Google Scholar]
- Goto T., Befus D., Low R., Bienenstock J. Mast cell heterogeneity and hyperplasia in bleomycin-induced pulmonary fibrosis of rats. Am Rev Respir Dis. 1984 Nov;130(5):797–802. doi: 10.1164/arrd.1984.130.5.797. [DOI] [PubMed] [Google Scholar]
- Guy-Grand D., Dy M., Luffau G., Vassalli P. Gut mucosal mast cells. Origin, traffic, and differentiation. J Exp Med. 1984 Jul 1;160(1):12–28. doi: 10.1084/jem.160.1.12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haig D. M., Jarrett E. E., Tas J. In vitro studies on mast cell proliferation in N. brasiliensis infection. Immunology. 1984 Apr;51(4):643–651. [PMC free article] [PubMed] [Google Scholar]
- Haig D. M., McKee T. A., Jarrett E. E., Woodbury R., Miller H. R. Generation of mucosal mast cells is stimulated in vitro by factors derived from T cells of helminth-infected rats. Nature. 1982 Nov 11;300(5888):188–190. doi: 10.1038/300188a0. [DOI] [PubMed] [Google Scholar]
- Haig D. M., McMenamin C., Redmond J., Brown D., Young I. G., Cohen S. D., Hapel A. J. Rat IL-3 stimulates the growth of rat mucosal mast cells in culture. Immunology. 1988 Oct;65(2):205–211. [PMC free article] [PubMed] [Google Scholar]
- Holt P. G., McMenamin C. Defence against allergic sensitization in the healthy lung: the role of inhalation tolerance. Clin Exp Allergy. 1989 May;19(3):255–262. doi: 10.1111/j.1365-2222.1989.tb02380.x. [DOI] [PubMed] [Google Scholar]
- Huntley J. F., McGorum B., Newlands G. F., Miller H. R. Granulated intraepithelial lymphocytes: their relationship to mucosal mast cells and globule leucocytes in the rat. Immunology. 1984 Nov;53(3):525–535. [PMC free article] [PubMed] [Google Scholar]
- Irani A. A., Schechter N. M., Craig S. S., DeBlois G., Schwartz L. B. Two types of human mast cells that have distinct neutral protease compositions. Proc Natl Acad Sci U S A. 1986 Jun;83(12):4464–4468. doi: 10.1073/pnas.83.12.4464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Karlsson T., Ellerson J. R., Dahlbom I., Bennich H. Analysis of the serum IgE levels in nonimmunized rats of various strains by a radioimmunoassay. Scand J Immunol. 1979 Mar;9(3):217–228. doi: 10.1111/j.1365-3083.1979.tb02725.x. [DOI] [PubMed] [Google Scholar]
- Kent J. F. Distribution and fine structure of globule leucocytes in respiratory and digestive tracts of the laboratory rat. Anat Rec. 1966 Dec;156(4):439–453. doi: 10.1002/ar.1091560408. [DOI] [PubMed] [Google Scholar]
- Marks R. M., Roche W. R., Czerniecki M., Penny R., Nelson D. S. Mast cell granules cause proliferation of human microvascular endothelial cells. Lab Invest. 1986 Sep;55(3):289–294. [PubMed] [Google Scholar]
- Mayrhofer G. The nature of the thymus dependency of mucosal mast cells. II. The effect of thymectomy and of depleting recirculating lymphocytes on the response to Nippostrongylus brasilliensis. Cell Immunol. 1979 Oct;47(2):312–322. doi: 10.1016/0008-8749(79)90341-1. [DOI] [PubMed] [Google Scholar]
- McMenamin C. C., Gault E. A., Haig D. M. The effect of dexamethasone on growth and differentiation of bone-marrow derived mucosal mast cells in vitro. Immunology. 1987 Sep;62(1):29–34. [PMC free article] [PubMed] [Google Scholar]
- McMenamin C., Jarrett E. E., Sanderson A. Surface phenotype of T cells producing growth of mucosal mast cells in normal rat bone marrow culture. Immunology. 1985 Jul;55(3):399–403. [PMC free article] [PubMed] [Google Scholar]
- Miller H. R., Jarrett W. F. Immune reactions in mucous membranes. I. Intestinal mast cell response during helminth expulsion in the rat. Immunology. 1971 Mar;20(3):277–288. [PMC free article] [PubMed] [Google Scholar]
- Newlands G. F., Huntley J. F., Miller H. R. Concomitant detection of mucosal mast cells and eosinophils in the intestines of normal and Nippostrongylus-immune rats. A re-evaluation of histochemical and immunocytochemical techniques. Histochemistry. 1984;81(6):585–589. doi: 10.1007/BF00489539. [DOI] [PubMed] [Google Scholar]
- Strobel S., Miller H. R., Ferguson A. Human intestinal mucosal mast cells: evaluation of fixation and staining techniques. J Clin Pathol. 1981 Aug;34(8):851–858. doi: 10.1136/jcp.34.8.851. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tam E. K., Calonico L. D., Nadel J. A., McDonald D. M. Globule leukocytes and mast cells in the rat trachea: their number, distribution, and response to compound 48/80 and dexamethasone. Anat Embryol (Berl) 1988;178(2):107–118. doi: 10.1007/BF02463644. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Viegas M., Gomez E., Brooks J., Davies R. J. Changes in nasal mast cell numbers in and out of the pollen season. Int Arch Allergy Appl Immunol. 1987;82(3-4):275–276. doi: 10.1159/000234205. [DOI] [PubMed] [Google Scholar]
- Woodbury R. G., Gruzenski G. M., Lagunoff D. Immunofluorescent localization of a serine protease in rat small intestine. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2785–2789. doi: 10.1073/pnas.75.6.2785. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woodbury R. G., Neurath H. Purification of an atypical mast cell protease and its levels in developing rats. Biochemistry. 1978 Oct 3;17(20):4298–4304. doi: 10.1021/bi00613a029. [DOI] [PubMed] [Google Scholar]
