JAK-STAT Pathway Regulation of Intestinal Permeability: Pathogenic Roles and Therapeutic Opportunities in Inflammatory Bowel Disease

被引：26

作者：

Lei, Hillmin ^{[1
]}

Crawford, Meli'sa S. ^{[1
]}

McCole, Declan F. ^{[1
]}

机构：

[1] Univ Calif Riverside, Sch Med, Div Biomed Sci, Riverside, CA 92521 USA

来源：

PHARMACEUTICALS | 2021年 / 14卷 / 09期

基金：

美国国家卫生研究院;

关键词：

tight junctions; intestinal permeability; inflammatory bowel disease; JAK-STAT; PROTEIN-TYROSINE-PHOSPHATASE; JUNCTIONAL ADHESION MOLECULE; EPITHELIAL TIGHT JUNCTIONS; CROHNS-DISEASE; CLAUDIN-2; EXPRESSION; ULCERATIVE-COLITIS; BARRIER; DYSFUNCTION; TOFACITINIB; TRICELLULIN;

D O I：

10.3390/ph14090840

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

The epithelial barrier forms the interface between luminal microbes and the host immune system and is the first site of exposure to many of the environmental factors that trigger disease activity in chronic inflammatory bowel disease (IBD). Disruption of the epithelial barrier, in the form of increased intestinal permeability, is a feature of IBD and other inflammatory diseases, including celiac disease and type 1 diabetes. Variants in genes that regulate or belong to the JAK-STAT signaling pathway are associated with IBD risk. Inhibitors of the JAK-STAT pathway are now effective therapeutic options in IBD. This review will discuss emerging evidence that JAK inhibitors can be used to improve defects in intestinal permeability and how this plays a key role in resolving intestinal inflammation.

引用

页数：14

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