IL-17F deficiency inhibits small intestinal tumorigenesis in ApcMin/+ mice

被引:42
作者
Chae, Wook-Jin [1 ]
Bothwell, Alfred L. M. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
关键词
IL-17; Tumor immunity; Inflammation; TH17; CELLS; HOST-DEFENSE; MOUSE MODEL; RESPONSES; PROTEIN; CANCER; INTERLEUKIN-17A; IDENTIFICATION; POLYPOSIS; ROLES;
D O I
10.1016/j.bbrc.2011.09.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IL-17 plays an important role in gut homeostasis. However, the role of IL-17F in intestinal tumorigenesis has not been addressed. Here we demonstrate that ablation of IL-17F significantly inhibits spontaneous intestinal tumorigenesis in the small intestine of Apc(Min/+) mice. IL-17F ablation decreased IL-1 beta and Cox-2 expression as well as IL-17 receptor C (IL-17RC) expression, which were increased in tumors from Apc(Min/+). mice. Lack of IL-17F did not reverse the splenomegaly but partially restored thymic atrophy, suggesting a local effect of IL-17F in the intestine. IL-17F deficient Apc(Min/+) mice showed a significant decrease in immune cell infiltration in the lamina propria. Interestingly, the expression of IL-17A from CD4 T cells in the lamina propria remains unchanged in the absence of IL-17F. Collectively, our results suggest the proinflammatory and essential role of IL-17F to develop spontaneous intestinal tumorigenesis in Apc(Min/+) mice in the presence of IL-17A. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:31 / 36
页数:6
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