A major role for proteolytic activity and proteinase-activated receptor-2 in the pathogenesis of infectious colitis

被引:154
作者
Hansen, KK
Sherman, PM
Cellars, L
Andrade-Gordon, P
Pan, ZY
Baruch, A
Wallace, JL
Hollenberg, MD
Vergnolle, N [1 ]
机构
[1] Univ Calgary, Dept Pharmacol & Therapeut, Mucosal Inflammat Res Grp, Proteinases & Inflammat Network, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Fac Med, Dept Med, Calgary, AB T2N 1N4, Canada
[3] Univ Toronto, Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[4] Celera Genom, San Francisco, CA 94080 USA
[5] Johnson & Johnson Pharmaceut Res & Dev, Drug Discovery, Spring House, PA 19477 USA
关键词
colitis; inflammation; trypsin; granzyme;
D O I
10.1073/pnas.0409535102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Citrobacter rodentium is a bacterial pathogen that causes a murine infectious colitis equivalent to enterohemorrhagic Escherichia coli infection in humans. Colonic luminal fluid from C. rodentium-infected mice, but not from sham-infected mice, contains active serine proteinases that can activate proteinase-activated receptor-2 (PAR(2)) We have identified granzyme A and murine trypsins to be present in C. rodentium-infected luminal fluid, as determined by mass spectrometry and Western blot analysis. Inflammatory indices (colonic mucosa macroscopic damage score, increased intestinal wall thickness, granulocyte infiltration, and bacterial translocation from the colonic lumen to peritoneal organs) were all increased in C. rodentium-infected mice, compared with sham-infected mice. Soybean trypsin inhibitor-treated wild-type mice and untreated PAR(2)-deficient (PAR(2)(-/-)) mice (compared with their wild-type littermates) both had substantially reduced levels of C. rodentium-induced inflammation. These data point to an important role for both pathogen-induced host serine proteinases and PAR2 in the setting of infectious colitis.
引用
收藏
页码:8363 / 8368
页数:6
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