Intestinal mucosal mast cells in normal and nematode-infected rat intestines are in intimate contact with peptidergic nerves
- PMID: 2437589
- PMCID: PMC304783
- DOI: 10.1073/pnas.84.9.2975
Intestinal mucosal mast cells in normal and nematode-infected rat intestines are in intimate contact with peptidergic nerves
Abstract
Inflammatory or allergic conditions, as well as situations where healing and repair processes occur, are characterized by the presence of increased numbers of mast cells. Previous work on the effect of neuropeptides on mast cell mediator release showed that only substance P caused such release from intestinal mucosal mast cells [Shanahan, F., Denburg, J. A., Fox, J., Bienenstock, J. & Befus, A. D. (1985) J. Immunol. 135, 1331-1337]. Accordingly, we investigated the microanatomical relationship between mast cells and enteric nerves in normal rat intestine and parasite-infected rat intestine, in which mucosal mast cell hyperplasia occurs. Combined immunohistochemistry for neuron-specific enolase and staining with alcian blue at pH 0.5 was employed on paraffin-embedded sections of normal and Nippostrongylus brasiliensis-infected rat jejunum. Sixty-seven percent of intestinal mucosal mast cells were touching subepithelial nerves, and an additional 20% were within 2 micron of nerves. Assessment of the proportion of the lamina propria occupied by mast cells (12.5%), the average mast cell area (121 +/- 28 microns 2), and the density of enteric nerves (one per 788 +/- 151 microns 2) suggested that the association was 5 times greater than would be expected by chance alone (P less than 0.0001). In consecutive sections, the nerves in contact with mast cells were also shown to contain substance P and/or calcitonin-gene-related peptide. Electron microscopy confirmed this association: 8% of the mast cells in infected rats exhibited membrane-membrane contact with unmyelinated axons containing 70- to 170-nm dense-core vesicles, and an additional 31% were situated less than 250 nm from nerves. Other mast cells appeared to embrace nerve bundles through the projection of lamellopodia. These data provide systematic quantitative evidence that a structural foundation for communication between the immune and nervous systems exists in the rat gastrointestinal tract.
Similar articles
-
Remodeling of B-50 (GAP-43)- and NSE-immunoreactive mucosal nerves in the intestines of rats infected with Nippostrongylus brasiliensis.J Neurosci. 1991 Dec;11(12):3809-21. doi: 10.1523/JNEUROSCI.11-12-03809.1991. J Neurosci. 1991. PMID: 1836018 Free PMC article.
-
Anatomical variation in mast cell nerve associations in the rat small intestine, heart, lung, and skin. Similarities of distances between neural processes and mast cells, eosinophils, or plasma cells in the jejunal lamina propria.Lab Invest. 1990 May;62(5):626-34. Lab Invest. 1990. PMID: 2342332
-
The role of mast cells in inflammatory processes: evidence for nerve/mast cell interactions.Int Arch Allergy Appl Immunol. 1987;82(3-4):238-43. doi: 10.1159/000234197. Int Arch Allergy Appl Immunol. 1987. PMID: 2437039 Review.
-
Mucosal mast cells are functionally active during spontaneous expulsion of intestinal nematode infections in rat.Nature. 1984 Nov 29-Dec 5;312(5993):450-2. doi: 10.1038/312450a0. Nature. 1984. PMID: 6504156
-
Innervation of mucosal immune cells in the gastrointestinal tract.Reg Immunol. 1992 Mar-Apr;4(2):91-9. Reg Immunol. 1992. PMID: 1354471 Review.
Cited by
-
Cellular Organization of Neuroimmune Interactions in the Gastrointestinal Tract.Trends Immunol. 2016 Jul;37(7):487-501. doi: 10.1016/j.it.2016.05.003. Epub 2016 Jun 9. Trends Immunol. 2016. PMID: 27289177 Free PMC article. Review.
-
Periarteriolar localization of mast cells promotes oriented interstitial migration of leukocytes in the hamster cheek pouch.Am J Pathol. 1989 Jan;134(1):161-9. Am J Pathol. 1989. PMID: 2536521 Free PMC article.
-
Delayed goblet cell hyperplasia, acetylcholine receptor expression, and worm expulsion in SMC-specific IL-4Ralpha-deficient mice.PLoS Pathog. 2007 Jan;3(1):e1. doi: 10.1371/journal.ppat.0030001. PLoS Pathog. 2007. PMID: 17222057 Free PMC article. Clinical Trial.
-
CP-96,345, a substance P antagonist, inhibits rat intestinal responses to Clostridium difficile toxin A but not cholera toxin.Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):947-51. doi: 10.1073/pnas.91.3.947. Proc Natl Acad Sci U S A. 1994. PMID: 7508124 Free PMC article.
-
Intestinal epithelial function: the case for immunophysiological regulation. Implications for disease (2).Dig Dis Sci. 1993 Sep;38(9):1735-45. doi: 10.1007/BF01303185. Dig Dis Sci. 1993. PMID: 8359088 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources