|
|
||||||||
Published online before print December 23, 2004
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Article |
,
,
*Department of Microbiology and Immunology, University of California, Davis; and
Department of Internal Medicine I, Robert Bosch Hospital and Dr. Margarete Fischer Bosch Institute, Stuttgart, Germany
| Abstract |
|---|
Crohns disease is a chronic, inflammatory disease of the intestinal mucosa. Although intestinal bacteria are implicated in disease pathogenesis, the etiology is still unclear. The main location of disease is the small intestine (ileum) and the colon. Ileal disease has been linked to a mutation in the NOD2 gene. Defensins are antimicrobial peptides and in the ileum, are mainly expressed in Paneth cells, epithelial cells that also express NOD2. In the colon, defensins are expressed by enterocytes or metaplastic Paneth cells. Crohns disease patients with ileal involvement, compared with controls or Crohns patients without ileal involvement, have diminished expression of ileal Paneth cell defensins. This decrease is even more pronounced in Crohns patients displaying a NOD2 mutation. In contrast, Crohns disease of the colon is characterized by an impaired induction of
-defensins in enterocytes. The colonic expression of the constitutive
-defensin 1 is also decreased in the inflamed colonic mucosa, but this decrease is less specific to Crohns disease, as it can also be found in ulcerative colitis patients. In conclusion, the regional localizations of Crohns disease, ileal or colonic disease, can be linked to different defensin profiles. Crohns disease of the ileum is associated with diminished defensin expression in Paneth cells. Crohns disease of the colon is associated with diminished
-defensin expression in enterocytes. Thus, it can be speculated that decreased defensin levels lead to a weakened intestinal barrier function to intestinal microbes and might be crucial in the pathophysiology of Crohns disease.
Key Words: NOD2 Paneth cells probiotic bacteria E. coli Nissle 1917
This article has been cited by other articles:
![]() |
T Fishbein, G Novitskiy, L Mishra, C Matsumoto, S Kaufman, S Goyal, K Shetty, L Johnson, A Lu, A Wang, et al. NOD2-expressing bone marrow-derived cells appear to regulate epithelial innate immunity of the transplanted human small intestine Gut, March 1, 2008; 57(3): 323 - 330. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Nuding, K. Fellermann, J. Wehkamp, and E. F Stange Reduced mucosal antimicrobial activity in Crohn's disease of the colon Gut, September 1, 2007; 56(9): 1240 - 1247. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. F. Skibola, J. D. Curry, and A. Nieters Genetic susceptibility to lymphoma Haematologica, July 1, 2007; 92(7): 960 - 969. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Schmid, K. Fellermann, P. Fritz, O. Wiedow, E. F. Stange, and J. Wehkamp Attenuated induction of epithelial and leukocyte serine antiproteases elafin and secretory leukocyte protease inhibitor in Crohn's disease J. Leukoc. Biol., April 1, 2007; 81(4): 907 - 915. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Voss, J. Wehkamp, K. Wehkamp, E. F. Stange, J. M. Schroder, and J. Harder NOD2/CARD15 Mediates Induction of the Antimicrobial Peptide Human Beta-defensin-2 J. Biol. Chem., January 27, 2006; 281(4): 2005 - 2011. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |