From intestinal stem cells to inflammatory bowel diseases

被引:99
作者
Gersemann, Michael [1 ,2 ,3 ]
Stange, Eduard Friedrich [1 ,2 ,3 ]
Wehkamp, Jan [1 ,2 ,3 ]
机构
[1] Robert Bosch Krankenhaus, D-70376 Stuttgart, Germany
[2] Univ Tubingen, D-70376 Stuttgart, Germany
[3] Dr Margarete Fischer Bosch Inst Clin Pharmacol, D-70376 Stuttgart, Germany
关键词
Inflammatory bowel disease; Paneth cells; Goblet cells; Cell differentiation; TCF4; Hath1; KLF4; ILEAL CROHNS-DISEASE; ALPHA-DEFENSIN EXPRESSION; ANTIMICROBIAL PEPTIDES; ULCERATIVE-COLITIS; INNATE IMMUNITY; GOBLET CELLS; DIFFERENTIATION; MUCUS; COLON; LAYER;
D O I
10.3748/wjg.v17.i27.3198
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
The pathogenesis of both entities of inflammatory bowel disease (IBD), namely Crohn's disease (CD) and ulcerative colitis (UC), is still complex and under investigation. The importance of the microbial flora in developing IBD is beyond debate. In the last few years, the focus has changed from adaptive towards innate immunity. Crohn's ileitis is associated with a deficiency of the antimicrobial shield, as shown by a reduced expression and secretion of the Paneth cell defensin HD5 and HD6, which is related to a Paneth cell differentiation defect mediated by a diminished expression of the Wnt transcription factor TCF4. In UC, the protective mucus layer, acting as a physical and chemical barrier between the gut epithelium and the luminal microbes, is thinner and in part denuded as compared to controls. This could be caused by a missing induction of the goblet cell differentiation factors Hath1 and KLF4 leading to immature goblet cells. This defective Paneth and goblet cell differentiation in Crohn's ileitis and UC may enable the luminal microbes to invade the mucosa and trigger the inflammation. The exact molecular mechanisms behind ileal CD and also UC must be further clarified, but these observations could give rise to new therapeutic strategies based on a stimulation of the protective innate immune system. (C) 2011 Baishideng. All rights reserved.
引用
收藏
页码:3198 / 3203
页数:6
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