Brandenburg Julius, Reiling Norbert
Microbial Interface Biology, Priority Research Area Infections, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Front Immunol. 2016 Dec 26;7:635. doi: 10.3389/fimmu.2016.00635. eCollection 2016.
In recent years, it has become apparent that the Wnt signaling pathway, known for its essential functions in embryonic development and tissue homeostasis, exerts immunomodulatory functions during inflammation and infection. Most functional studies indicate that Wnt5a exerts pro-inflammatory functions on its cellular targets, which include various types of immune and non-immune cells. Wnt5a expression has also been linked to the pathogenesis of chronic inflammatory diseases. Activation of beta-catenin-dependent Wnt signaling, e.g., by Wnt3a, has however been shown to limit inflammation by interfering with the nuclear factor kappa-light chain-enhancer of activated B-cells (NF-kappaB) pathway. This review focuses on the regulation of Wnt5a, Wnt3a, and the recently identified Wnt6 and their functional role in bacterial infections with a primary focus on pulmonary tuberculosis, a leading infectious cause of morbidity and mortality worldwide.
近年来,有一点已变得很明显,即因在胚胎发育和组织稳态中发挥重要功能而闻名的Wnt信号通路,在炎症和感染期间发挥免疫调节功能。大多数功能研究表明,Wnt5a对其细胞靶点发挥促炎功能,这些靶点包括各种类型的免疫细胞和非免疫细胞。Wnt5a的表达也与慢性炎症性疾病的发病机制有关。然而,已表明激活β-连环蛋白依赖性Wnt信号(例如通过Wnt3a)可通过干扰活化B细胞的核因子κB(NF-κB)通路来限制炎症。本综述重点关注Wnt5a、Wnt3a以及最近发现的Wnt6的调节及其在细菌感染中的功能作用,主要关注肺结核,它是全球发病率和死亡率的主要感染原因。