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首页> 外文期刊>Biochemical and Biophysical Research Communications >IL-17F deficiency inhibits small intestinal tumorigenesis in ApcMin/+ mice.
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IL-17F deficiency inhibits small intestinal tumorigenesis in ApcMin/+ mice.

机译:IL-17F缺乏会抑制ApcMin / +小鼠的小肠肿瘤发生。

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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-1beta 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.
机译:IL-17在肠道稳态中起重要作用。但是,IL-17F在肠道肿瘤发生中的作用尚未得到解决。在这里,我们证明消融IL-17F在Apc(Min / +)小鼠小肠中显着抑制了自发性肠肿瘤的发生。 IL-17F消融可降低Apc(Min / +)小鼠的肿瘤中IL-1beta和Cox-2表达以及IL-17受体C(IL-17RC)表达。缺乏IL-17F不能逆转脾肿大,但可以部分恢复胸腺萎缩,提示IL-17F在肠道中具有局部作用。 IL-17F缺陷型Apc(Min / +)小鼠在固有层中免疫细胞浸润明显减少。有趣的是,在没有IL-17F的情况下,固有层中CD4T细胞中IL-17A的表达保持不变。总的来说,我们的结果表明,在存在IL-17A的情况下,IL-17F在Apc(Min / +)小鼠中发展自发性肠肿瘤的促炎作用和必不可少的作用。

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