Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases

Author:

Jakubowska Katarzyna1,Pryczynicz Anna1,Iwanowicz Piotr1,Niewiński Andrzej2,Maciorkowska Elżbieta3,Hapanowicz Jerzy4,Jagodzińska Dorota1,Kemona Andrzej1,Guzińska-Ustymowicz Katarzyna1

Affiliation:

1. Department of General Pathomorphology, Medical University of Bialystok, Waszyngtona Street 13, 15-269 Bialystok, Poland

2. Department of Rehabilitation, Medical University of Bialystok, Bialystok, Poland

3. Department of Developmental Age Medicine and Paediatric Nursing, Medical University of Bialystok, Bialystok, Poland

4. Department of Oncological Surgery, Comprehensive Cancer Centre, Bialystok, Poland

Abstract

Crohn’s disease (CD) and ulcerative colitis (UC) belong to a group of inflammatory bowel diseases (IBD). The aim of our study was to evaluate the expression of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 in ulcerative colitis and Crohn’s disease. The study group comprised 34 patients with UC and 10 patients with CD. Evaluation of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 expression in tissue samples was performed using immunohistochemistry. The overexpression of MMP-9 and TIMP-1 was dominant in both the glandular epithelium and inflammatory infiltration in UC patients. In contrast, in CD subjects the positive expression of MMP-2 and TIMP-1 was in glandular tubes while mainly MMP-7 and TIMP-2 expression was in inflammatory infiltration. Metalloproteinases’ expression was associated with the presence of erosions, architectural tissue changes, and inflammatory infiltration in the lamina propria of UC patients. The expression of metalloproteinase inhibitors correlated with the presence of eosinophils and neutrophils in UC and granulomas in CD patients. Our studies indicate that the overexpression of metalloproteinases and weaker expression of their inhibitors may determine the development of IBD. It appears that MMP-2, MMP-7, and MMP-9 may be a potential therapeutic target and the use of their inhibitors may significantly reduce UC progression.

Publisher

Hindawi Limited

Subject

Gastroenterology,Hepatology

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