Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993 Nov;94(2):341-7.
doi: 10.1111/j.1365-2249.1993.tb03455.x.

Altered expression of cell adhesion molecules in uninvolved gut in inflammatory bowel disease

Affiliations

Altered expression of cell adhesion molecules in uninvolved gut in inflammatory bowel disease

G M Schuermann et al. Clin Exp Immunol. 1993 Nov.

Abstract

Adhesion of circulating cells to vascular endothelium occurs in the early phase of inflammation, and is mediated by specific cell adhesion molecules. Many such adhesion molecules are increased in inflamed regions of ulcerative colitis (UC) and Crohn's disease (CD) but there is limited knowledge of their expression in the uninvolved gut, adjacent to inflammation. We investigated immunohistochemically the expression of platelet endothelial cell adhesion molecule-1 (PECAM-1), intercellular adhesion molecule-1 (ICAM-1) and lymphocyte function-associated antigen-1 (LFA-1) on resected specimens taken at a distance of 2-4 cm from the inflamed area and without histological signs of inflammation. Compared with normal gut, we found (i) a significant increase of PECAM-1-positive vessels in the mucosa of uninvolved UC (149.0 +/- 24.1 vessels/mm2 (mean +/- s.d.); normal colon = 123.1 +/- 21.6; P = 0.004); (ii) a significant decrease of ICAM-1-positive vessels in uninvolved CD (111.9 +/- 22.6 vessels/mm2; normal ileum = 136.9 +/- 27.6; P = 0.04); and (iii) a moderate but statistically insignificant increase of LFA-1-positive cells in the mucosa of uninvolved UC and Crohn's ileitis. This altered expression of cell adhesion molecules may contribute to the early lesion in inflammatory bowel disease and provide new therapeutic opportunities.

PubMed Disclaimer

References

    1. Gastroenterology. 1980 Nov;79(5 Pt 1):853-60 - PubMed
    1. Gut. 1993 Feb;34(2):247-51 - PubMed
    1. Gut. 1984 Jan;25(1):57-61 - PubMed
    1. Ann Surg. 1985 Jan;201(1):53-63 - PubMed
    1. Gastroenterology. 1986 May;90(5 Pt 1):1121-8 - PubMed

Publication types

MeSH terms

Substances