Mucin gene expression in intestinal epithelial cells in Crohn's disease

被引:131
作者
Buisine, MP
Desreumaux, P
Leteurtre, E
Copin, MC
Colombel, JF
Porchet, N
Aubert, JP
机构
[1] INSERM, U377, F-59045 Lille, France
[2] CHRU, Hop C Huriez, Lab Biochim & Biol, Lille, France
[3] CHRU, Equipe INSERM 0114, Lille, France
[4] Ctr Hosp Reg & Univ Lille, Hop Huriez, Serv Malad Appareil Digestif & Nutr, F-59037 Lille, France
[5] CHRU, Hop A Calmette, Lille, France
[6] Fac Med H Warembourg, Lab Anat & Cytol Pathol, Lille, France
[7] Univ Lille 2, Fac Med H Warembourg, Lille, France
关键词
mucins; MUC genes; Crohn's disease; ulcer associated cell lineage;
D O I
10.1136/gut.49.4.544
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Crohn's disease (CD) is a chronic relapsing inflammatory bowel disease of unknown origin. It is characterised by chronic mucosal ulcerations which affect any part of the intestine but most commonly are found in the ileum and proximal colon. Aims-Studies were undertaken to provide information regarding cell specific expression of mucin genes in the ileum of patients with CD. Patients and methods-Expression of mucin genes was analysed in the ileal mucosa of patients with CD and controls by in situ hybridisation and immunohistochemistry. Results-In healthy ileal mucosa, patients with CD showed a pattern identical to normal controls with main expression of MUC2 and MUC3, lesser expression of MUC1 and MUC4, and no expression of MUC5AC, MUC5B, MUC6, or MUC7. In the involved mucosa, the pattern was somewhat comparable although heterogeneous to that observed in healthy ileal mucosa. Importantly, a particular mucin gene expression pattern was observed in ileal mucosa close to the ulcer margins in ulcer associated cell lineage, with the appearance of MUC5AC and MUC6 mRNAs and peptides, which are normally restricted to the stomach (MUC5AC and MUC6) and duodenum (MUC6), and disappearance of MUC2. Conclusions-Our results suggest that gel forming mucins (more particularly MUC5AC and MUC6) may have a role in epithelial wound healing after mucosal injury in inflammatory bowel diseases in addition to mucosal protection.
引用
收藏
页码:544 / 551
页数:8
相关论文
共 47 条
[41]   The carboxyl-terminal sequence of the human secretory mucin, MUC6 - Analysis of the primary amino acid sequence [J].
Toribara, NW ;
Ho, SB ;
Gum, JR ;
Lau, P ;
Kim, YS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (26) :16398-16403
[42]   MUCIN GENE STRUCTURE AND EXPRESSION - PROTECTION VS ADHESION [J].
VANKLINKEN, BJW ;
DEKKER, J ;
BULLER, HA ;
EINERHAND, AWC .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 269 (05) :G613-G627
[43]   Expression of MUC2 and MUC3 mRNA in human normal, malignant, and inflammatory intestinal tissues [J].
Weiss, AA ;
Babyatsky, MW ;
Ogata, S ;
Chen, A ;
Itzkowitz, SH .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1996, 44 (10) :1161-1166
[44]   MUC5B is a major gel-forming, oligomeric mucin from human salivary gland, respiratory tract and endocervix:: identification of glycoforms and C-terminal cleavage [J].
Wickström, C ;
Davies, JR ;
Eriksen, GV ;
Veerman, ECI ;
Carlstedt, I .
BIOCHEMICAL JOURNAL, 1998, 334 :685-693
[45]  
Williams SJ, 1999, CANCER RES, V59, P4083
[46]   INDUCTION OF A NOVEL EPIDERMAL GROWTH FACTOR-SECRETING CELL LINEAGE BY MUCOSAL ULCERATION IN HUMAN GASTROINTESTINAL STEM-CELLS [J].
WRIGHT, NA ;
PIKE, C ;
ELIA, G .
NATURE, 1990, 343 (6253) :82-85
[47]   TREFOIL PEPTIDE GENE-EXPRESSION IN GASTROINTESTINAL EPITHELIAL-CELLS IN INFLAMMATORY BOWEL-DISEASE [J].
WRIGHT, NA ;
POULSOM, R ;
STAMP, G ;
VANNOORDEN, S ;
SARRAF, C ;
ELIA, G ;
AHNEN, D ;
JEFFERY, R ;
LONGCROFT, J ;
PIKE, C ;
RIO, MC ;
CHAMBON, P .
GASTROENTEROLOGY, 1993, 104 (01) :12-20