2009, Number 3
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Rev Med Hosp Gen Mex 2009; 72 (3)
Morphologic changes induced by stress in the population of Paneth cells
Martínez GDI, Camacho AJ, Villanueva BI, Becerril MA
Language: Spanish
References: 26
Page: 129-135
PDF size: 240.00 Kb.
ABSTRACT
Introduction: The mucous membrane of the small intestine forms villi that are covered by epithelium that is extended between the villi into the lamina propria to form the crypts of Lieberkühn. Paneth cells (PC) are found lying at the bottom of these crypts. They show acidophilic granules into their cytoplasm containing zinc, lysozymes, phospholipase A, IgA and other antimicrobial peptides. Induction of stress causes disturbances in physiological homeostasis that activate the hypothalamus-hypophysis-adrenal axis and the autonomic nervous system, thus resulting in corticoid and catecholamine release.
Objective: To study the effects of stress on the morphology and population of the PC along the small intestine of adult rats.
Material and methods: Eighteen Wistar male rats were divided in three groups, one control and two study groups in which a stressful forced swimming-condition, whether acute or chronic, was applied, and samples of the small intestine were obtained after perfusion with PFA. Five-micron slices were obtained from the tissue samples by histological processing, and stained by Gomori trichrome, wheat lectine or rodamine coupled- anti-alpha-defensin immunodetection. Slides were analyzed under optic microscope for PC number and granule content.
Results: An increase in PC density and granule content was seen in stress-exposed groups, but not in control group. The increase in the number of cells can be interpreted as an effect of stress stimulating the maturation rate of PC, and the increase in granule content suggests that stress induces the functional activation of these cells.
Conclusions: It is concluded that the PC population is affected by stress in a way that increases its activity.
REFERENCES
Rumio C, Besusso D, Palazzo M, Selleri S, Sfondrini L, Dubini F, Ménard S, Balsari A. Degranulation of Paneth Cells via Toll-Like Receptor 9. Am J Pathol 2004; 165 (2): 373–381.
Fawcett DW. Tratado de histología. 12a ed. México: Interamericana-McGraw-Hill; 1995. p. 646-658.
Geneser F. Histología. 3a ed. México: Panamericana; 2003. p. 498-505.
Elphick DA, Mahida YR. Paneth cells: Their role in innate immunity and inflammatory disease. Gut 2005; 54: 1802-1809.
Gent A, Creamer B. Paneth cells secretion. Digestion 1972; 7: 1–12.
Shimada O, Ishikawa H, Tosaka–Shimada H, Yasuda T, Kishi K, Suzuki S. Detection of deoxyribonuclease I along the secretory pathway in Paneth cells of human small intestine. J Histochem Cytochem 1998; 46; 833-840.
Bevins CL. Events at the host-microbial interface of the gastrointestinal tract. V. Paneth cell alpha-defensins in intestinal host defense. Am J Physiol Gastrointest Liver Physiol 2005; 289: 173-176.
Guyton AC, Hall J. Tratado Fisiología Médica. México; McGraw–Hill-Interamericana; 2002. p. 817-818.
Pohlmeyer I, Jorns J, Schumacher U, Van Dame M, Peumans W, Pfuller U. Lectin histochemical investigations of the distal gut chicks with special emphasis on the follicle–associated epithelium. J Vet Med 2005; 52: 138-146.
Andreu P, Colnot S, Godard C, Gad S, Chafey P, Niwa-Kawakita M, Laurent-Puig P, Kahn A, Robine S, Perret C, Romagnolo B. Crypt-restricted proliferation and commitment to the Paneth cell lineage following Apc loss in the mouse intestine. Development 2005; 132: 1443-1451.
Batlle E, Henderson JT, Beghtel H, van den Born MM, Sancho E, Huls G, Meeldijk J, Robertson J, van de Wetering M, Pawson T, Clevers H. Beta-catenin and TCF mediate cell positioning in the intestinal epithelium by controlling the expression of EphB/ephrinB. Cell 2002; 111: 251-263.
Leis O, Madrid JF, Ballesta J, Hernández FN. An O-linked oligosaccharides in the secretory granules of rat Paneth cells: an ultrastructural cytochemical study. J Histo Cytochem 1997; 45: 285-293.
Jarillo, A. Becerril, A. Detección citoquímica de fucosa y ácido siálico/N-acetil-glucosamina en células de Paneth. Memorias Second Interamerican Congress on Electron Microscopy, Cancún Q.R.
Wehkamp J, Salzman NH, Porter E, Nuding S, Weichenthal M, Petras RE, Shen B, Schaeffeler E, Schwab M, Linzmeier R, Feathers RW, Chu H, Lima H Jr, Fellermann K, Ganz T, Stange EF, Bevins CL. Reduced Paneth cell {alpha}-defensins in ileal Crohn’s disease. Proc Natl Acad Sci USA 2005.
Ouellette AJ. Paneth cell alpha-defensins: peptide mediators of innate immunity in the small intestine. Springer Semin Immunopathol 2005; 27: 133-146.
Inada K, Tanaka H, Nakanishi H, Tsukamoto T, Ikehara Y, Tatematsu K, Nakamura S, Porter EM, Tatematsu M. Identification of Paneth cells in pyloric glands associated with gastric and intestinal mixed-type intestinal metaplasia of the human stomach. Virchows Arch 2001; 439: 14-20.
Hao HN, Zhao J, Lotoczky G, Grever WE, Lyman WD. Induction of human beta-defensin-2 expression in human astrocytes by lipopolysaccharide and cytokines. J Neurochem 2001; 77: 1027-1035.
Kamdar K, Maemoto A, Qu X, Young SK, Ouellette AJ. In vitro activation of the rhesus macaque myeloid alpha-defensin precursor proRMAD-4 by neutrophil serine proteinases. J Biol Chem 2008; 283 (47): 32361-8.
Satoh Y, Yamano M, Matsuda M. Ultrastructure of Paneth cells in the intestine of various mammals, J Electron Microsc Tech 1990; 16: 69–80.
Sundstrom G, Helander H. Quantitative electron microscopic studies on rat ileal Paneth cells under various physiological and experimental conditions. Hepatogastroenterology 1980; 27: 286–293.
Briones AA, Rocha L, Picazo O. Influence of forced swimming stress on 5-HT1A receptors and serotonin levels in mouse brain. Progress in neuro_farmacology and biological psichiatry 2005; 29: 275-281.
Porter E, Yang H, Yavagal S, Preza GC, Murillo O, Lima H, Greene S, Mahoozi L, Klein-Patel M, Diamond G, Gulati S, Ganz T, Rice PA, Quayle AJ. Distinct defensin profiles in Neisseria gonorrhoeae and Chlamydia trachomatis urethritis reveal novel epithelial cell-neutrophil interactions. Infect Immun 2005; 73: 4823-4833.
Batlle E, Henderson JT, Beghtel H, van den Born MM, Sancho E, Huls G, Meeldijk J, Robertson J, van de Wetering M, Pawson T, Clevers H. Beta-catenin and TCF mediate cell positioning in the intestinal epithelium by controlling the expression of EphB/ephrinB. Cell 2002; 111: 251-263.
Yang HS, Hinds PW. pRb-mediated control of epithelial cell proliferation and Indian hedgehog expression in mouse intestinal development. BMC Dev Biol 2007; 26; 7: 6.
Dinsdale D, Biles B. Postnatal changes in the distribution and elemental composition of Paneth cells in normal and corticosteroid–treated rats. Cell Tissue Res 1986; 246: 183-187.
Briones AA, Rocha L, Picazo O. Alterations in GABAergic function following forced swimming stress. Farmacology biochemistry and behavior 2005; 80: 463-470.