Receptor for advanced glycation endproducts mediates neutrophil migration across intestinal epithelium

被引:65
|
作者
Zen, Ke
Chen, Celia X. -J.
Chen, Yi-Tien
Wilton, Rosemarie
Liu, Yuan
机构
[1] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[2] Argonne Natl Lab, Div Biosci, Argonne, IL 60439 USA
来源
JOURNAL OF IMMUNOLOGY | 2007年 / 178卷 / 04期
关键词
D O I
10.4049/jimmunol.178.4.2483
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Receptor for advanced glyeation endproducts (RAGE) is an Ig superfamily cell surface receptor that interacts with a diverse array of ligands associated with inflammatory responses. In this study, we provide evidence demonstrating that RAGE is involved in inflammatory responses in the intestines. We showed that RAGE is expressed in intestinal epithelial cells, primarily concentrated at the lateral membranes close to the apical cell junction complexes. Although RAGE expression was low in epithelium under normal conditions, this protein was up-regulated after treatment with the inflammatory cytokines IFN-gamma and/or TNF-alpha. RAGE expression was also elevated in colon tissue samples from patients with inflammatory bowel diseases. Using in vitro transmigration assays, we found that RAGE mediates neutrophil (polymorphonuclear leukocytes (PMN)) adhesion to, and subsequent migration across, intestinal epithelial monolayers. This activity appears to be mediated by the binding of RAGE to the PMN-specific beta(2) integrin CD11b/CD18. Thus, these results provide a novel mechanism for the regulation of PMN transepithelial migration and may suggest a new therapeutic target for intestinal inflammation.
引用
收藏
页码:2483 / 2490
页数:8
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