Guanylate-binding protein-1 is expressed at tight junctions of intestinal epithelial cells in response to interferon-γ and regulates barrier function through effects on apoptosis

被引:53
作者
Schnoor, M. [1 ]
Betanzos, A. [1 ]
Weber, D. A. [1 ]
Parkos, C. A. [1 ]
机构
[1] Emory Univ, Dept Pathol & Lab Med, Epithelial Pathobiol Unit, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
INFLAMMATORY-BOWEL-DISEASE; NECROSIS-FACTOR-ALPHA; ENDOTHELIAL-CELLS; IL-10-DEFICIENT MICE; ACTIVATION; VIRUS; INHIBITION; INDUCTION; GENETICS; RECEPTOR;
D O I
10.1038/mi.2008.62
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Guanylate-binding protein-1 (GBP-1) is an interferon inducible large GTPase involved in endothelial cell proliferation and invasion. In this report, expression and function of GBP-1 were investigated in vitro in intestinal epithelia after exposure to interferon-gamma and in human colonic mucosa from individuals with inflammatory bowel disease (IBD). Interestingly, in contrast to other epithelia, GBP-1 distributed to the plasma membrane in intestinal epithelial cells where it colocalized with the tight junction protein coxsackie- and adenovirus receptor. In addition, expression of GBP-1 was upregulated in colonic epithelia of individuals with IBD. Downregulation of GBP-1 by siRNA resulted in enhanced permeability that correlated with increased apoptosis. Indeed, inhibition of caspase activity prevented the inhibition of barrier formation induced by the loss of GBP-1. These data suggest that GBP-1 is a novel marker of intestinal mucosal inflammation that may protect against epithelial apoptosis induced by inflammatory cytokines and subsequent loss of barrier function.
引用
收藏
页码:33 / 42
页数:10
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