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HECT E3 泛素连接酶 Nedd4 对于抗真菌固有免疫是必需的。

HECT E3 Ubiquitin Ligase Nedd4 Is Required for Antifungal Innate Immunity.

机构信息

Biomedical Science Graduate Program, Ohio State University, Columbus, OH; and.

Department of Pathology, University of Iowa, Iowa City, IA.

出版信息

J Immunol. 2021 Aug 1;207(3):868-877. doi: 10.4049/jimmunol.2100083. Epub 2021 Jul 19.

Abstract

is the most common cause of fungal infections in humans, and disseminated candidiasis has become one of the leading causes of hospital-acquired bloodstream infections with a high mortality rate. However, little is known about the host-pathogen interactions and the mechanisms of antifungal immunity. Here, we report that Nedd4 (neuronal precursor cell-expressed developmentally downregulated 4) is essential for signaling through Dectin-1 and Dectin-2/3. We showed that mice that lack Nedd4 globally or only in the myeloid compartment are highly susceptible to systemic infection, which correlates with heightened organ fungal burden, defective inflammatory response, impaired leukocyte recruitment to the kidneys, and defective reactive oxygen species expression by granulocytes. At the molecular level, macrophages displayed impaired activation of TGF-β-activating kinase-1 and NF-κB, but normal activation of spleen tyrosine kinase and protein kinase C-δ on yeast and hyphal infections. These data suggest that Nedd4 regulates signaling events downstream of protein kinase C-δ but upstream of or at TGF-β-activating kinase-1.

摘要

念珠菌是人类最常见的真菌感染原因,而播散性念珠菌病已成为导致医院获得性血流感染的主要原因之一,死亡率很高。然而,人们对宿主-病原体相互作用和抗真菌免疫机制知之甚少。在这里,我们报告 Nedd4(神经前体细胞表达的发育下调 4)对于 Dectin-1 和 Dectin-2/3 的信号转导是必不可少的。我们表明,全身性或仅在髓样细胞中缺乏 Nedd4 的小鼠对系统性感染非常敏感,这与器官真菌负荷增加、炎症反应缺陷、白细胞向肾脏募集受损以及粒细胞中活性氧物质表达缺陷有关。在分子水平上,在酵母和菌丝感染时,巨噬细胞显示 TGF-β-激活激酶-1 和 NF-κB 的激活受损,但脾酪氨酸激酶和蛋白激酶 C-δ 的激活正常。这些数据表明,Nedd4 调节蛋白激酶 C-δ 下游的信号事件,但在 TGF-β-激活激酶-1 之前或之上。

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本文引用的文献

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