Claudin-2 as a mediator of leaky gut barrier during intestinal inflammation

被引:203
作者
Luettig, J. [1 ]
Rosenthal, R. [1 ]
Barmeyer, C. [1 ]
Schulzke, J. D. [1 ]
机构
[1] Inst Clin Physiol, Dept Gastroenterol, Berlin, Germany
来源
TISSUE BARRIERS | 2015年 / 3卷 / 1-2期
关键词
celiac disease; claudin-2; Crohn's disease; HIV; IFN gamma; inflammatory bowel disease; TNF alpha; tight junction; ulcerative colitis;
D O I
10.4161/21688370.2014.977176
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The epithelial tight junction determines the paracellular water and ion movement in the intestine and also prevents uptake of larger molecules, including antigens, in an uncontrolled manner. Claudin-2, one of the 27 mammalian claudins regulating that barrier function, forms a paracellular channel for small cations and water. It is typically expressed in leaky epithelia like proximal nephron and small intestine and provides a major pathway for the paracellular transport of sodium, potassium, and fluid. In intestinal inflammation (Crohn's disease, ulcerative colitis), immune-mediated diseases (celiac disease), and infections (HIV enteropathy), claudin-2 is upregulated in small and large intestine and contributes to diarrhea via a leak flux mechanism. In parallel to that upregulation, other epithelial and tight junctional features are altered and the luminal uptake of antigenic macromolecules is enhanced, for which claudin-2 may be partially responsible through induction of tight junction strand discontinuities.
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页数:10
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