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IFN-γ 和 TNF-α 诱导的 GBP-1 通过抑制 β-连环蛋白/TCF 信号通路抑制上皮细胞增殖。

IFN-γ and TNF-α-induced GBP-1 inhibits epithelial cell proliferation through suppression of β-catenin/TCF signaling.

机构信息

Epithelial Pathobiology Research Unit, Department of Pathology and Laboratory of Medicine, Emory University, Atlanta, GA, USA.

出版信息

Mucosal Immunol. 2012 Nov;5(6):681-90. doi: 10.1038/mi.2012.41. Epub 2012 Jun 13.

Abstract

Proinflammatory cytokines induce guanylate-binding protein 1 (GBP-1) protein expression in intestinal epithelial tissues. GBP-1 has been described as influencing a number of cellular processes important for epithelial homeostasis, including cell proliferation. However, many questions remain as to the role of GBP-1 in intestinal mucosal homeostasis. We therefore sought to investigate the function of proinflammatory cytokine-induced GBP-1 during intestinal epithelial cell proliferation. Through the use of complementary GBP-1 overexpression and small interfering RNA-mediated knockdown studies, we now show that GBP-1 acts to inhibit pro-mitogenic β-catenin/T cell factor (TCF) signaling. Interestingly, proinflammatory cytokine-induced GBP-1 was found to be a potent suppressor of β-catenin protein levels and β-catenin serine 552 phosphorylation. Neither glycogen synthase kinase 3β nor proteasomal inhibition alleviated GBP-1-mediated suppression of cell proliferation or β-catenin/TCF signaling, indicating a non-canonical mechanism of β-catenin inhibition. Together, these data show that cytokine-induced GBP-1 retards cell proliferation by forming a negative feedback loop that suppresses β-catenin/TCF signaling.

摘要

促炎细胞因子诱导肠上皮组织中鸟嘌呤核苷酸结合蛋白 1(GBP-1)蛋白的表达。GBP-1 已被描述为影响许多对上皮细胞稳态很重要的细胞过程,包括细胞增殖。然而,GBP-1 在肠黏膜稳态中的作用仍有许多问题需要研究。因此,我们试图研究促炎细胞因子诱导的 GBP-1 在肠上皮细胞增殖中的功能。通过使用互补的 GBP-1 过表达和小干扰 RNA 介导的敲低研究,我们现在表明 GBP-1 抑制促有丝分裂 β-连环蛋白/T 细胞因子(TCF)信号。有趣的是,发现促炎细胞因子诱导的 GBP-1 是β-连环蛋白蛋白水平和β-连环蛋白丝氨酸 552 磷酸化的有效抑制剂。糖原合酶激酶 3β 或蛋白酶体抑制均不能缓解 GBP-1 介导的细胞增殖或β-连环蛋白/TCF 信号的抑制,表明存在β-连环蛋白抑制的非经典机制。这些数据表明,细胞因子诱导的 GBP-1 通过形成负反馈环抑制β-连环蛋白/TCF 信号,从而减缓细胞增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37bf/3481006/5268e5e8c891/nihms-383219-f0001.jpg

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