神经毒性
生物
星形胶质细胞
调解人
干扰素
免疫学
小胶质细胞
疾病
病理
中枢神经系统
神经科学
炎症
细胞生物学
医学
毒性
内科学
作者
Barney Viengkhou,Emina Hayashida,Sarah McGlasson,Katie Emelianova,Deborah Forbes,Stewart Wiseman,Joanna M. Wardlaw,Katie Emelianova,Sarosh Irani,Darragh Duffy,Fredrik Piehl,Lipin Loo,Axel Pagenstecher,G. Gregory Neely,Yanick J. Crow,Iain L. Campbell,David Hunt,Markus J. Hofer
出处
期刊:Immunity
[Elsevier]
日期:2024-06-01
被引量:2
标识
DOI:10.1016/j.immuni.2024.05.017
摘要
Aicardi-Goutières syndrome (AGS) is an autoinflammatory disease characterized by aberrant interferon (IFN)-α production. The major cause of morbidity in AGS is brain disease, yet the primary source and target of neurotoxic IFN-α remain unclear. Here, we demonstrated that the brain was the primary source of neurotoxic IFN-α in AGS and confirmed the neurotoxicity of intracerebral IFN-α using astrocyte-driven Ifna1 misexpression in mice. Using single-cell RNA sequencing, we demonstrated that intracerebral IFN-α-activated receptor (IFNAR) signaling within cerebral endothelial cells caused a distinctive cerebral small vessel disease similar to that observed in individuals with AGS. Magnetic resonance imaging (MRI) and single-molecule ELISA revealed that central and not peripheral IFN-α was the primary determinant of microvascular disease in humans. Ablation of endothelial Ifnar1 in mice rescued microvascular disease, stopped the development of diffuse brain disease, and prolonged lifespan. These results identify the cerebral microvasculature as a primary mediator of IFN-α neurotoxicity in AGS, representing an accessible target for therapeutic intervention.
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