Defensins and inflammation: The role of defensins in inflammatory bowel disease

被引:137
作者
Ramasundara, Malith [2 ]
Leach, Steven T. [2 ]
Lemberg, Daniel A. [1 ]
Day, Andrew S. [1 ,2 ]
机构
[1] Sydney Childrens Hosp, Dept Gastroenterol, Sydney, NSW, Australia
[2] Univ New S Wales, Sch Womens & Childrens Hlth, Sydney, NSW 2052, Australia
基金
英国医学研究理事会;
关键词
Crohn disease; defensins; HBD; HD; inflammatory bowel disease; intestinal bacteria; NOD2; ulcerative colitis; GENOME-WIDE ASSOCIATION; NOD2; CARD15; MUTATIONS; PANETH CELL DEFENSINS; ILEAL CROHNS-DISEASE; ANTIMICROBIAL PEPTIDES; ULCERATIVE-COLITIS; EPITHELIAL-CELLS; INNATE IMMUNITY; HUMAN BETA-DEFENSIN-2; ALPHA-DEFENSINS;
D O I
10.1111/j.1440-1746.2008.05772.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Defensins are antimicrobial peptides produced at a variety of epithelial surfaces. In the intestinal tract, they contribute to host immunity and assist in maintaining the balance between protection from pathogens and tolerance to normal flora. However, attenuated expression of defensins compromises host immunity and hence may alter the balance toward inflammation. Altered defensin production is suggested to be an integral element in the pathogenesis of inflammatory bowel disease (IBD). Evidence for this is shown in Crohn's disease where reduced alpha-defensin levels are seen in patients with ileal disease and reduced beta-defensin levels in those with colonic involvement. Further evidence is provided by research linking nucleotide oligomerization domain 2 (NOD2) mutations and deficient defensin expression. However, alternate studies suggest that NOD2 status and defensin expression are independent, and that defensin deficiency is due to mucosal surface destruction as a result of inflammatory changes, indicating that reduced defensin expression is a symptom of the disease and not the cause. Although it is clear that defensin expression is altered in IBD, it is less clear whether defensin deficiency is implicated in the pathogenesis of IBD or is a consequence of the disease process. The aim of this article is to review the current knowledge of defensins in IBD and discuss their potential role in IBD pathogenesis.
引用
收藏
页码:202 / 208
页数:7
相关论文
共 40 条
[31]   Microbial influences in inflammatory bowel diseases [J].
Sartor, R. Balfour .
GASTROENTEROLOGY, 2008, 134 (02) :577-594
[32]   Reduced α-defensin expression is associated with inflammation and not NOD2 mutation status in ileal Crohn's disease [J].
Simms, L. A. ;
Doecke, J. D. ;
Walsh, M. D. ;
Huang, N. ;
Fowler, E. V. ;
Radford-Smith, G. L. .
GUT, 2008, 57 (07) :903-910
[33]   Denatured human α-defensin attenuates the bactericidal activity and the stability against enzymatic digestion [J].
Tanabe, Hiroki ;
Ayabe, Tokiyoshi ;
Maemoto, Atsuo ;
Ishikawa, Chisato ;
Inaba, Yuhei ;
Sato, Ryu ;
Moriichi, Kentaro ;
Okamoto, Kotaro ;
Watari, Jiro ;
Kono, Toru ;
Ashida, Toshifumi ;
Kohgo, Yutaka .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 358 (01) :349-355
[34]   NOD2/CARD15 mediates induction of the antimicrobial peptide human beta-defensin-2 [J].
Voss, E ;
Wehkamp, J ;
Wehkamp, K ;
Stange, EF ;
Schröder, JM ;
Harder, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (04) :2005-2011
[35]   Reduced Paneth cell α-defensins in ileal Crohn's disease [J].
Wehkamp, J ;
Salzman, NH ;
Porter, E ;
Nuding, S ;
Weichenthal, M ;
Petras, RE ;
Shen, B ;
Schaeffeler, E ;
Schwab, M ;
Linzmeier, R ;
Feathers, RW ;
Chu, HT ;
Lima, H ;
Fellermann, K ;
Ganz, T ;
Stange, EF ;
Bevins, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (50) :18129-18134
[36]   NOD2 (CARD15) mutations in Crohn's disease are associated with diminished mucosal α-defensin expression [J].
Wehkamp, J ;
Harder, J ;
Weichenthal, M ;
Schwab, M ;
Schäffeler, E ;
Schlee, M ;
Herrlinger, KR ;
Stallmach, A ;
Noack, F ;
Fritz, P ;
Schröder, JM ;
Bevins, CL ;
Fellermann, K ;
Stange, EF .
GUT, 2004, 53 (11) :1658-1664
[37]   Inducible and constitutive β-defensins are differentially expressed in Crohn's disease and ulcerative colitis [J].
Wehkamp, J ;
Harder, J ;
Weichenthal, M ;
Mueller, O ;
Herrlinger, KR ;
Fellermann, K ;
Schroeder, JM ;
Stange, EF .
INFLAMMATORY BOWEL DISEASES, 2003, 9 (04) :215-223
[38]   Human β-defensin 2 but not β-defensin 1 is expressed preferentially in colonic mucosa of inflammatory bowel disease [J].
Wehkamp, J ;
Fellermann, K ;
Herrlinger, KR ;
Baxmann, S ;
Schmidt, K ;
Schwind, B ;
Duchrow, M ;
Wohlschläger, C ;
Feller, AC ;
Stange, EF .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2002, 14 (07) :745-752
[39]   Defensins and other antimicrobial peptides in inflammatory bowel disease [J].
Wehkamp, Jan ;
Schmid, Michael ;
Stange, Eduard F. .
CURRENT OPINION IN GASTROENTEROLOGY, 2007, 23 (04) :370-378
[40]   Paneth cell antimicrobial peptides: Topographical distribution and quantification in human gastrointestinal tissues [J].
Wehkamp, Jan ;
Chu, Hiutung ;
Shen, Bo ;
Feathers, Ryan W. ;
Kays, Robert J. ;
Lee, Sarah K. ;
Bevins, Charles L. .
FEBS LETTERS, 2006, 580 (22) :5344-5350