Thymic Stromal Lymphopoetin-Induced Expression of the Endogenous Inhibitory Enzyme SLPI Mediates Recovery from Colonic Inflammation

被引:99
作者
Reardon, Colin [1 ]
Lechmann, Matthias [1 ]
Bruestle, Anne [1 ]
Gareau, Melanie G. [2 ]
Shuman, Naomi [1 ]
Philpott, Dana [3 ]
Ziegler, Steven F. [4 ]
Mak, Tak W. [1 ]
机构
[1] Univ Hlth Network, Ontario Canc Inst, Campbell Family Canc Res Inst, Toronto, ON M5G 2C1, Canada
[2] Hosp Sick Children, Res Inst, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
[4] Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
基金
加拿大健康研究院;
关键词
NF-KAPPA-B; SECRETORY LEUKOPROTEASE INHIBITOR; INTESTINAL IMMUNE HOMEOSTASIS; DENDRITIC CELLS; EPITHELIAL-CELLS; EXPERIMENTAL COLITIS; PRIMARY CULTURES; T-CELLS; TSLP; MICE;
D O I
10.1016/j.immuni.2011.05.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymic stromal lymphopoetin (TSLP) influences numerous immune functions, including those in the colonic mucosa. Here we report that TSLP-deficient (Tslp(-/-)) mice did not exhibit increased inflammation during dextran sodium sulfate (DSS)-induced colitis but failed to recover from disease, resulting in death. Increased localized neutrophil elastase (NE) activity during overt inflammation was observed in Tslp(-/-) mice and was paralleled by reduced expression of an endogenous inhibitor, secretory leukocyte peptidase inhibitor (SLPI). Pharmacological inhibition of NE or treatment with rSLPI reduced DSS-induced mortality in Tslp(-/-) mice. Signaling through TSLPR on nonhematopoietic cells was sufficient for recovery from DSS-induced colitis. Expression of the receptor occurred on intestinal epithelial cells (IEC), with stimulation inducing SLPI expression. Therefore, TSLP is critical in mediating mucosal healing after insult and functions in a nonredundant capacity that is independent of restraining T helper 1 (Th1) and Th17 cell cytokine production.
引用
收藏
页码:223 / 235
页数:13
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