Enteroaggregative Escherichia coli promotes transepithelial migration of neutrophils through a conserved 12-lipoxygenase pathway

被引:24
|
作者
Boll, Erik J. [1 ,2 ]
Struve, Carsten [2 ]
Sander, Anja [1 ,2 ]
Demma, Zachary [1 ]
Krogfelt, Karen A. [2 ]
McCormick, Beth A. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst, Worcester, MA 01609 USA
[2] Statens Serum Inst, Dept Microbiol Surveillance & Res, Copenhagen, Denmark
基金
美国国家卫生研究院;
关键词
INFLAMMATORY-BOWEL-DISEASE; PROTEIN-KINASE-C; INTESTINAL EPITHELIAL MONOLAYERS; SHIGELLA-FLEXNERI; HEPOXILIN A(3); ARACHIDONATE; 12-LIPOXYGENASE; PHOSPHOLIPASE A(2); BIOLOGICAL IMPLICATIONS; AGGREGATIVE ADHERENCE; CELL MONOLAYERS;
D O I
10.1111/j.1462-5822.2011.01706.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Enteroaggregative Escherichia coli (EAEC) induces release of pro-inflammatory markers and disruption of intestinal epithelial barriers in vitro, suggesting an inflammatory aspect to EAEC infection. However, the mechanisms underlying EAEC-induced mucosal inflammatory responses and the extent to which these events contribute to pathogenesis is not well characterized. Employing an established in vitro model we demonstrated that EAEC prototype strain 042 induces migration of polymorphonuclear neutrophils (PMNs) across polarized T84 cell monolayers. This event was mediated through a conserved host cell signalling cascade involving the 12/15-LOX pathway and led to apical secretion of an arachidonic acid-derived lipid PMN chemoattractant, guiding PMNs across the epithelia to the site of infection. Moreover, supporting the hypothesis that inflammatory responses may contribute to EAEC pathogenesis, we found that PMN transepithelial migration promoted enhanced attachment of EAEC 042 to T84 cells. These findings suggest that EAEC-induced PMN infiltration may favour colonization and thus pathogenesis of EAEC.
引用
收藏
页码:120 / 132
页数:13
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