Differential expression of mucosal addressin cell adhesion molecule-1 (MAdCAM-1) in ulcerative colitis and Crohn's disease

被引:123
作者
Arihiro, S
Ohtani, H
Suzuki, M
Murata, M
Ejima, C
Oki, M
Kinouchi, Y
Fukushima, K
Sasaki, I
Nakamura, S
Matsumoto, T
Torii, A
Toda, G
Nagura, H
机构
[1] Tohoku Univ, Grad Sch Med, Dept Pathol, Sendai, Miyagi 980, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Gastroenterol, Sendai, Miyagi 980, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Surg, Div Biol Response & Oncol, Sendai, Miyagi 980, Japan
[4] Jikei Univ, Sch Med, Dept Internal Med, Div Gastroenterol & Hepatol, Tokyo, Japan
[5] Osaka City Univ, Grad Sch Med, Dept Gastroenterol, Osaka 558, Japan
关键词
Crohn's disease; gut-associated lymphocytes; lymphocyte homing; mucosal addressin cell adhesion molecule-1 (MAdCAM-1); transmural inflammation; ulcerative colitis;
D O I
10.1046/j.1440-1827.2002.01365.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Mucosal addressin cell adhesion molecule-1 (MAdCAM-1) is selectively expressed in the endothelial cells of intestinal mucosa and gut-associated lymphoid tissue (GALT). Engagement of MAdCAM-1 to its ligand, integrin alpha(4)beta(7) , on lymphocytes is associated with the homing of gut-associated lymphocytes to normal gastrointestinal tract and inflammation sites. The present study was designed to elucidate differences between Crohn's disease (CrD) and ulcerative colitis (UC) from the expression patterns of MAdCAM-1. Samples were taken from 40 patients with CrD and 24 patients with UC at surgical resection. Using frozen sections, immunohistochemistry was performed for MAdCAM-1, E-selectin and CD34. MAdCAM-1(+) venules were abundant in inflamed mucosa in both UC and CrD. In contrast, clear differences were noted between UC and CrD in the inflammatory area in the ulcer base, that is, MAdCAM-1(+) venules were more abundant in CrD than in UC (P < 0.001), while E-selectin was expressed equally in these venules in both diseases. Furthermore, CrD was characterized by the occurrence of MAdCAM-1(+) venules in deeper layers of the intestinal tissue, mainly in lymphoid aggregates. Our data indicated more extensive expression of MAdCAM-1 in CrD, which could contribute not only to mucosal inflammation, but also to transmural inflammation in CrD.
引用
收藏
页码:367 / 374
页数:8
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