Host-Toxoplasma Interaction Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom.
Immunobiology Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom.
J Immunol. 2018 Jul 15;201(2):604-614. doi: 10.4049/jimmunol.1701322. Epub 2018 Jun 11.
IFN-stimulated gene (ISG) 15 is a ubiquitin-like protein induced after type I IFN stimulation. There is a dearth of in vivo models to study free unconjugated ISG15 function. We found that free ISG15 enhances the production of IFN-γ and IL-1β during murine infection with In our model, ISG15 is induced in a type I IFN-dependent fashion and released into the serum. Increased ISG15 levels are dependent on an actively invading and replicating parasite. Two cysteine residues in the hinge domain are necessary determinants for ISG15 to induce increased cytokine levels during infection. Increased ISG15 is concurrent with an influx of IL-1β-producing CD8α dendritic cells to the site of infection. In this article, we present infection as a novel in vivo murine model to study the immunomodulatory properties of free ISG15 and uniquely link it to IL-1β production by CD8α dendritic cells driven by two cysteines in the hinge region of the protein.
干扰素刺激基因(ISG)15 是一种在 I 型干扰素刺激后诱导产生的泛素样蛋白。目前缺乏用于研究游离未缀合 ISG15 功能的体内模型。我们发现,游离 ISG15 可增强小鼠感染时 IFN-γ 和 IL-1β 的产生。在我们的模型中,ISG15 以 I 型 IFN 依赖性方式诱导,并释放到血清中。ISG15 水平的增加依赖于活跃入侵和复制的寄生虫。铰链域中的两个半胱氨酸残基是 ISG15 在感染过程中诱导细胞因子水平升高的必要决定因素。ISG15 的增加伴随着产生 IL-1β 的 CD8α 树突状细胞涌入感染部位。在本文中,我们提出 感染作为一种新的体内小鼠模型,用于研究游离 ISG15 的免疫调节特性,并将其与 hinge 区域的两个半胱氨酸驱动的 CD8α 树突状细胞产生的 IL-1β 独特地联系起来。