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Published on: April 21, 2015
Differential expression of mucosal addressin cell adhesion molecule-1 (MAdCAM-1) in ulcerative colitis and Crohn's
Seiji Arihiro1, Haruo Ohtani, Manabu Suzuki
1Department of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Insights
Mucosal addressin cell adhesion molecule-1 (MAdCAM-1) expression differs between Crohn's disease and ulcerative colitis. MAdCAM-1 is more abundant in Crohn's disease, potentially contributing to transmural inflammation.
Area of Science:
- Immunology
- Gastroenterology
- Cell Biology
Background:
- Mucosal addressin cell adhesion molecule-1 (MAdCAM-1) mediates lymphocyte homing to the gut.
- MAdCAM-1 plays a role in gastrointestinal tract inflammation.
Purpose of the Study:
- To investigate differential expression patterns of MAdCAM-1 in Crohn's disease (CrD) and ulcerative colitis (UC).
Main Methods:
- Immunohistochemistry was used to analyze MAdCAM-1, E-selectin, and CD34 expression in surgical resection samples from CrD and UC patients.
- Analysis focused on inflamed mucosa and ulcer bases.
Main Results:
- MAdCAM-1+ venules were prevalent in inflamed mucosa in both CrD and UC.
- Significantly higher MAdCAM-1+ venule abundance was observed in the ulcer base of CrD compared to UC.
- CrD exhibited MAdCAM-1+ venules in deeper intestinal layers and lymphoid aggregates.
Conclusions:
- Extensive MAdCAM-1 expression in Crohn's disease may contribute to both mucosal and transmural inflammation.
- Differential MAdCAM-1 expression could be a key factor distinguishing CrD from UC pathogenesis.
Abstract:
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 alpha4beta7, 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.
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