par Demetter, Pieter
;De Vos, Marc
;Van Damme, Nicole
;Baeten, D;Elewaut, D;Vermeulen, S;Mareel, Marcus;Bullock, G;Mielants, H;Verbruggen, G;De Keyser, Frédérique
;Veys, E M;Cuvelier, Claude A
Référence American journal of clinical pathology, 114, 3, page (364-370)
Publication Publié, 2000-09




Référence American journal of clinical pathology, 114, 3, page (364-370)
Publication Publié, 2000-09
Article révisé par les pairs
Résumé : | The E-cadherin-catenin complex is important for the maintenance of epithelial architecture. We studied its expression in Crohn disease, ulcerative colitis, acute ileitis, and controls. Immunohistochemical stainings for E-cadherin, alpha-catenin, beta-catenin and gamma-catenin were performed. E-cadherin messenger RNA (mRNA) was detected using riboprobes. In active inflammation, there was up-regulation of the complex. In particular, epithelium adjacent to ulcers showed increased expression of protein and mRNA, but in ulcer-associated cell lineage, the intensity of staining was weak to negative. In focal inflammation, up-regulation was found in affected areas. Reparative epithelium growing over denuded areas showed weaker expression. Since structural or functional perturbation in any of the molecules of the E-cadherin-catenin complex results in loss of intercellular adhesion, the preexistent epithelium may benefit from up-regulation to try to maintain its normal architecture under inflammatory conditions. Reduced expression in reparative epithelium and ulcer-associated cell lineage could facilitate the motility of these cells. |