Activation of nuclear factor kappa B in Crohn's disease
- PMID: 9865503
- DOI: 10.1007/s000110050358
Activation of nuclear factor kappa B in Crohn's disease
Abstract
Objectives and design: The location and degree of activation of nuclear factor kappa (NFkappaB), a primary transcription factor that plays a regulating role in immune and inflammatory responses, was determined in Crohn's disease using full thickness specimens of bowel collected at surgery.
Materials and methods: Resected specimens of inflamed and non-inflamed bowel were collected from thirteen patients with Crohn's disease and non-inflamed bowel from eleven control subjects. Prepared frozen sections were immunostained using a monoclonal antibody to the activated form of the p65 subunit of NFkappaB and the number of positive staining cells counted using a Lennox graticule.
Results: The number of cells positive for activated NFkappaB was significantly increased (p = 0.001 ) in all layers of inflamed Crohn's disease bowel, compared to non-inflamed bowel from controls. There was also a significant increase ( p = 0.009) in the number of positive cells, when compared to non-inflamed bowel from control subjects, in the submucosa of non-inflamed areas of Crohn's disease bowel. Cells positive for activated NFkappaB were provisionally identified by morphological criteria as mostly macrophages with some lymphocytes. There was no activation in endothelia.
Conclusion: NFkappaB is activated within large mononuclear cells in all layers of inflamed areas of the bowel in Crohn's disease and may represent key events in the inflammatory process. Increased activation in the submucosa of non-inflamed Crohn's disease bowel provides further evidence of early immunological activation in macroscopically and microscopically uninvolved areas and an underlying abnormal immune system in Crohn's disease.
Similar articles
-
Analysis of direct tissue isoelectric focused protein profiles of resected intestinal mucosa and endoscopic biopsies from patients with inflammatory bowel disease.Clin Invest Med. 1992 Feb;15(1):49-59. Clin Invest Med. 1992. PMID: 1374000
-
Functional characterisation of decoy receptor 3 in Crohn's disease.Gut. 2009 Apr;58(4):483-91. doi: 10.1136/gut.2008.148908. Epub 2008 Nov 27. Gut. 2009. PMID: 19039087
-
Immunohistochemical localization of vascular endothelial growth factor in colonic mucosa of patients with inflammatory bowel disease.Hepatogastroenterology. 2002 Jan-Feb;49(43):116-23. Hepatogastroenterology. 2002. PMID: 11941933
-
Concepts of oxidative stress and antioxidant defense in Crohn's disease.World J Gastroenterol. 2013 Oct 21;19(39):6540-7. doi: 10.3748/wjg.v19.i39.6540. World J Gastroenterol. 2013. PMID: 24151379 Free PMC article. Review.
-
Contribution of morphology for the comprehension of mechanisms of fibrosis in inflammatory enterocolitis.Acta Gastroenterol Belg. 2000 Oct-Dec;63(4):371-6. Acta Gastroenterol Belg. 2000. PMID: 11233520 Review.
Cited by
-
Human serum-derived hydroxy long-chain fatty acids exhibit anti-inflammatory and anti-proliferative activity.J Exp Clin Cancer Res. 2011 May 17;30(1):59. doi: 10.1186/1756-9966-30-59. J Exp Clin Cancer Res. 2011. PMID: 21586136 Free PMC article.
-
NF-kappa B activation correlates with disease phenotype in Crohn's disease.PLoS One. 2017 Jul 28;12(7):e0182071. doi: 10.1371/journal.pone.0182071. eCollection 2017. PLoS One. 2017. PMID: 28753650 Free PMC article.
-
Lipopolysaccharide and silica-stimulated mononuclear cell prostaglandin production in ulcerative colitis.Mediators Inflamm. 2000;9(3-4):189-91. doi: 10.1080/09629350020002903. Mediators Inflamm. 2000. PMID: 11132777 Free PMC article.
-
Dissociated invasively growing cancer cells with NF-kappaB/p65 positivity after radiotherapy: a new marker for worse clinical outcome in rectal cancer? Preliminary data.Clin Exp Metastasis. 2008;25(4):491-6. doi: 10.1007/s10585-008-9155-5. Epub 2008 Mar 7. Clin Exp Metastasis. 2008. PMID: 18324356
-
Mapping Transcriptome Data to Protein-Protein Interaction Networks of Inflammatory Bowel Diseases Reveals Disease-Specific Subnetworks.Front Genet. 2021 Aug 18;12:688447. doi: 10.3389/fgene.2021.688447. eCollection 2021. Front Genet. 2021. PMID: 34484291 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical