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β-连环蛋白在树突状细胞中的激活调节肠道中的免疫与耐受。

Activation of beta-catenin in dendritic cells regulates immunity versus tolerance in the intestine.

机构信息

Emory Vaccine Center, and Yerkes National Primate Research Center, 954 Gatewood Road, Atlanta, GA 30329, USA.

出版信息

Science. 2010 Aug 13;329(5993):849-53. doi: 10.1126/science.1188510.

Abstract

Dendritic cells (DCs) play a vital role in initiating robust immunity against pathogens as well as maintaining immunological tolerance to self antigens. However, the intracellular signaling networks that program DCs to become tolerogenic remain unknown. We report here that the Wnt-beta-catenin signaling in intestinal dendritic cells regulates the balance between inflammatory versus regulatory responses in the gut. beta-catenin in intestinal dendritic cells was required for the expression of anti-inflammatory mediators such as retinoic acid-metabolizing enzymes, interleukin-10, and transforming growth factor-beta, and the stimulation of regulatory T cell induction while suppressing inflammatory effector T cells. Furthermore, ablation of beta-catenin expression in DCs enhanced inflammatory responses and disease in a mouse model of inflammatory bowel disease. Thus, beta-catenin signaling programs DCs to a tolerogenic state, limiting the inflammatory response.

摘要

树突状细胞(DCs)在启动针对病原体的强大免疫以及维持对自身抗原的免疫耐受方面发挥着至关重要的作用。然而,将 DC 编程为耐受性的细胞内信号网络仍不清楚。我们在这里报告,肠道树突状细胞中的 Wnt-β-catenin 信号调节了肠道中炎症与调节反应之间的平衡。肠道树突状细胞中的β-catenin 对于抗炎介质如视黄酸代谢酶、白细胞介素 10 和转化生长因子-β的表达以及调节性 T 细胞诱导的刺激是必需的,同时抑制炎症效应 T 细胞。此外,在炎症性肠病的小鼠模型中,树突状细胞中β-catenin 表达的缺失增强了炎症反应和疾病。因此,β-catenin 信号将 DC 编程为耐受性状态,限制了炎症反应。

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