Evidence of altered structural and secretory glycoconjugates in the jejunal mucosa of patients with gluten sensitive enteropathy and subtotal villous atrophy.
Journal: 1989/September - Gut
ISSN: 0017-5749
PUBMED: 2753405
Abstract:
The pattern of lectin histochemistry in formalin fixed, paraffin embedded normal jejunal and subtotal villous atrophy specimens from patients with gluten sensitive enteropathy were compared. There was no significant difference in the binding pattern of five lectins (Arachis hypogaea, Canavalia ensiformis, Lens culinaris, Phaseolus vulgaris and Triticum vulgaris) between normal and abnormal specimens. There were significant changes in the binding pattern of three lectins (Dolichos biflorus, Ulex europaeus, Ricinus communis), with special reference to goblet cells staining. These changes were present in all the specimens studied, regardless of the clinical diagnosis of dermatitis herpetiformis or coeliac disease. Dolichos biflorus reactive goblet cells were significantly decreased (p less than 0.001) in abnormal tissue and confined to the luminal edge of the mucosa. Strong reactivity of goblet cells in abnormal tissue was recorded with Ricinus communis and Ulex europaeus, lectins that bind to few or no goblet cells in normal tissue. These findings show that modifications of structural and secretory glycoconjugates occur in the jejunal mucosa of patients with gluten sensitive enteropathy.
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Gut 30(6): 804-810

Evidence of altered structural and secretory glycoconjugates in the jejunal mucosa of patients with gluten sensitive enteropathy and subtotal villous atrophy.

Abstract

The pattern of lectin histochemistry in formalin fixed, paraffin embedded normal jejunal and subtotal villous atrophy specimens from patients with gluten sensitive enteropathy were compared. There was no significant difference in the binding pattern of five lectins (Arachis hypogaea, Canavalia ensiformis, Lens culinaris, Phaseolus vulgaris and Triticum vulgaris) between normal and abnormal specimens. There were significant changes in the binding pattern of three lectins (Dolichos biflorus, Ulex europaeus, Ricinus communis), with special reference to goblet cells staining. These changes were present in all the specimens studied, regardless of the clinical diagnosis of dermatitis herpetiformis or coeliac disease. Dolichos biflorus reactive goblet cells were significantly decreased (p less than 0.001) in abnormal tissue and confined to the luminal edge of the mucosa. Strong reactivity of goblet cells in abnormal tissue was recorded with Ricinus communis and Ulex europaeus, lectins that bind to few or no goblet cells in normal tissue. These findings show that modifications of structural and secretory glycoconjugates occur in the jejunal mucosa of patients with gluten sensitive enteropathy.

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  • Sharon N, Lis H. Lectins: cell-agglutinating and sugar-specific proteins. Science. 1972 Sep 15;177(4053):949–959. [PubMed] [Google Scholar]
  • Brown JC, Hunt RC. Lectins. Int Rev Cytol. 1978;52:277–349. [PubMed] [Google Scholar]
  • Zieske JD, Bernstein IA. Epidermal fucosylation of cell surface glycoprotein. Biochem Biophys Res Commun. 1984 Mar 30;119(3):1028–1033. [PubMed] [Google Scholar]
  • Sieber-Blum M, Cohen AM. Lectin binding to neural crest cells. Changes of the cell surface during differentiation in vitro. J Cell Biol. 1978 Mar;76(3):628–638.[PMC free article] [PubMed] [Google Scholar]
  • Gorelick FS, Sarras MP, Jr, Jamieson JD. Regional differences in lectin binding to colonic epithelium by fluorescent and electron microscopy. J Histochem Cytochem. 1982 Nov;30(11):1097–1108. [PubMed] [Google Scholar]
  • Fischer J, Klein PJ, Vierbuchen M, Skutta B, Uhlenbruck G, Fischer R. Characterization of glycoconjugates of human gastrointestinal mucosa by lectins. I. Histochemical distribution of lectin binding sites in normal alimentary tract as well as in benign and malignant gastric neoplasms. J Histochem Cytochem. 1984 Jul;32(7):681–689. [PubMed] [Google Scholar]
  • Boland CR, Montgomery CK, Kim YS. Alterations in human colonic mucin occurring with cellular differentiation and malignant transformation. Proc Natl Acad Sci U S A. 1982 Mar;79(6):2051–2055.[PMC free article] [PubMed] [Google Scholar]
  • Jacobs LR, Huber PW. Regional distribution and alterations of lectin binding to colorectal mucin in mucosal biopsies from controls and subjects with inflammatory bowel diseases. J Clin Invest. 1985 Jan;75(1):112–118.[PMC free article] [PubMed] [Google Scholar]
  • Vecchi M, Torgano G, Monti M, Berti E, Agape D, Primignani M, Ronchi G, de Franchis R. Evaluation of structural and secretory glycoconjugates in normal human jejunum by means of lectin histochemistry. Histochemistry. 1987;86(4):359–364. [PubMed] [Google Scholar]
  • RUBIN CE, BRANDBORG LL, PHELPS PC, TAYLOR HC., Jr Studies of celiac disease. I. The apparent identical and specific nature of the duodenal and proximal jejunal lesion in celiac disease and idiopathic sprue. Gastroenterology. 1960 Jan;38:28–49. [PubMed] [Google Scholar]
  • YARDLEY JH, BAYLESS TM, NORTON JH, HENDRIX TR. Celiac disease. A study of the jejunal epithelium before and after a gluten-free diet. N Engl J Med. 1962 Dec 6;267:1173–1179. [PubMed] [Google Scholar]
  • Rubin W, Ross LL, Sleisenger MH, Weser E. An electron microscopic study of adult celiac disease. Lab Invest. 1966 Nov;15(11):1720–1747. [PubMed] [Google Scholar]
  • Marsh MN. The small intestine: mechanisms of local immunity and gluten sensitivity. Clin Sci (Lond) 1981 Nov;61(5):497–503. [PubMed] [Google Scholar]
  • Peters TJ, Bjarnason I. Coeliac syndrome: biochemical mechanisms and the missing peptidase hypothesis revisted. Gut. 1984 Sep;25(9):913–918.[PMC free article] [PubMed] [Google Scholar]
  • Weiser MM, Douglas AP. An alternative mechanism for gluten toxicity in coeliac disease. Lancet. 1976 Mar 13;1(7959):567–569. [PubMed] [Google Scholar]
  • Colyer J, Farthing MJ, Kumar PJ, Clark ML, Ohannesian AD, Waldron NM. Reappraisal of the 'lectin hypothesis' in the aetiopathogenesis of coeliac disease. Clin Sci (Lond) 1986 Jul;71(1):105–110. [PubMed] [Google Scholar]
  • deFranchis R, Primignani M, Cipolla M, Vecchi M, Agape D, Monti M, Berti E, Zuccato E, Mussini E. Small-bowel involvement in dermatitis herpetiformis and in linear-IgA bullous dermatosis. J Clin Gastroenterol. 1983 Oct;5(5):429–436. [PubMed] [Google Scholar]
  • Primignani M, Agape D, Ronchi G, Falsitta M, Cipolla M, Vecchi M, Torgano G, Monti M, Berti E, de Franchis R. Prevalence of duodenal and jejunal lesions in dermatitis herpetiformis. Ric Clin Lab. 1987 Jul-Sep;17(3):243–249. [PubMed] [Google Scholar]
  • Phelps CF. Biosynthesis of mucus glycoprotein. Br Med Bull. 1978 Jan;34(1):43–48. [PubMed] [Google Scholar]
  • Kim YS, Isaacs R, Perdomo JM. Alterations of membrane glycopeptides in human colonic adenocarcinoma. Proc Natl Acad Sci U S A. 1974 Dec;71(12):4869–4873.[PMC free article] [PubMed] [Google Scholar]
  • Kim YS, Perdomo J, Ochoa P, Isaacs RA. Regional and cellular localization of glycosyltransferases in rat small intestine. Changes in enzymes with differentiation of intestinal epithelial cells. Biochim Biophys Acta. 1975 May 23;391(1):39–50. [PubMed] [Google Scholar]
  • MACDONALD WC, TRIER JS, EVERETT NB. CELL PROLIFERATION AND MIGRATION IN THE STOMACH, DUODENUM, AND RECTUM OF MAN: RADIOAUTOGRAPHIC STUDIES. Gastroenterology. 1964 Apr;46:405–417. [PubMed] [Google Scholar]
  • SHORTER RG, MOERTEL CG, TITUS JL, REITEMEIER RJ. CELL KINETICS IN THE JEJUNUM AND RECTUM OF MAN. Am J Dig Dis. 1964 Nov;9:760–763. [PubMed] [Google Scholar]
  • Trier JS, Browning TH. Epithelial-cell renewal in cultured duodenal biopsies in celiac sprue. N Engl J Med. 1970 Dec 3;283(23):1245–1250. [PubMed] [Google Scholar]
  • Auricchio S, De Ritis G, De Vincenzi M, Mancini E, Minetti M, Sapora O, Silano V. Agglutinating activity of gliadin-derived peptides from bread wheat: implications for coeliac disease pathogenesis. Biochem Biophys Res Commun. 1984 Jun 15;121(2):428–433. [PubMed] [Google Scholar]
Istituto di Medicina Interna, Università di Milano, Italy.
Istituto di Medicina Interna, Università di Milano, Italy.
Abstract
The pattern of lectin histochemistry in formalin fixed, paraffin embedded normal jejunal and subtotal villous atrophy specimens from patients with gluten sensitive enteropathy were compared. There was no significant difference in the binding pattern of five lectins (Arachis hypogaea, Canavalia ensiformis, Lens culinaris, Phaseolus vulgaris and Triticum vulgaris) between normal and abnormal specimens. There were significant changes in the binding pattern of three lectins (Dolichos biflorus, Ulex europaeus, Ricinus communis), with special reference to goblet cells staining. These changes were present in all the specimens studied, regardless of the clinical diagnosis of dermatitis herpetiformis or coeliac disease. Dolichos biflorus reactive goblet cells were significantly decreased (p less than 0.001) in abnormal tissue and confined to the luminal edge of the mucosa. Strong reactivity of goblet cells in abnormal tissue was recorded with Ricinus communis and Ulex europaeus, lectins that bind to few or no goblet cells in normal tissue. These findings show that modifications of structural and secretory glycoconjugates occur in the jejunal mucosa of patients with gluten sensitive enteropathy.
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