TNF suppresses acute intestinal inflammation by inducing local glucocorticoid synthesis

被引:143
作者
Noti, Mario [1 ]
Corazza, Nadia [1 ]
Mueller, Christoph [1 ]
Berger, Barbara [2 ]
Brunner, Thomas [1 ]
机构
[1] Univ Bern, Div Expt Pathol, CH-3010 Bern, Switzerland
[2] Univ Bern, Div Cytopathol, Inst Pathol, CH-3010 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
TUMOR-NECROSIS-FACTOR; DEXTRAN SULFATE SODIUM; T-CELLS; EXPERIMENTAL COLITIS; EPITHELIAL-CELLS; BOWEL-DISEASE; FACTOR-ALPHA; IN-VIVO; MICE; PATHOGENESIS;
D O I
10.1084/jem.20090849
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although tumor necrosis factor (alpha) (TNF) exerts proinflammatory activities in a variety of diseases, including inflammatory bowel disease, there is increasing evidence for antiinflammatory actions of TNF. In contrast, glucocorticoids (GCs) are steroid hormones that suppress inflammation, at least in part by regulating the expression and action of TNF. We report that TNF induces extraadrenal production of immunoregulatory GCs in the intestinal mucosa during acute intestinal inflammation. The absence of TNF results in a lack of colonic GC synthesis and exacerbation of dextran sodium sulfate-induced colitis. TNF seems to promote local steroidogenesis by directly inducing steroidogenic enzymes in intestinal epithelial cells. Therapeutic administration of TNF induces GC synthesis in oxazolone-induced colitis and ameliorates intestinal inflammation, whereas inhibition of intestinal GC synthesis abrogates the therapeutic effect of TNF. These data show that TNF suppresses the pathogenesis of acute intestinal inflammation by promoting local steroidogenesis.
引用
收藏
页码:1057 / 1066
页数:10
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