Department of Pathology and Immunology, University of Geneva, 1211 Geneva, Switzerland.
Department of Basic Neuroscience, University of Geneva, 1205 Geneva, Switzerland.
Cell. 2018 Oct 4;175(2):458-471.e19. doi: 10.1016/j.cell.2018.07.049. Epub 2018 Aug 30.
Inflammatory disorders of the CNS are frequently accompanied by synaptic loss, which is thought to involve phagocytic microglia and complement components. However, the mechanisms accounting for aberrant synaptic connectivity in the context of CD8 T cell-driven neuronal damage are poorly understood. Here, we profiled the neuronal translatome in a murine model of encephalitis caused by CD8 T cells targeting antigenic neurons. Neuronal STAT1 signaling and downstream CCL2 expression were essential for apposition of phagocytes, ensuing synaptic loss and neurological disease. Analogous observations were made in the brains of Rasmussen's encephalitis patients. In this devastating CD8 T cell-driven autoimmune disease, neuronal STAT1 phosphorylation and CCL2 expression co-clustered with infiltrating CD8 T cells as well as phagocytes. Taken together, our findings uncover an active role of neurons in coordinating phagocyte-mediated synaptic loss and highlight neuronal STAT1 and CCL2 as critical steps in this process that are amenable to pharmacological interventions.
中枢神经系统的炎症性疾病常伴有突触丧失,这被认为涉及吞噬性小胶质细胞和补体成分。然而,CD8 T 细胞驱动的神经元损伤背景下异常突触连接的机制仍知之甚少。在这里,我们对 CD8 T 细胞靶向抗原神经元引起的脑炎的小鼠模型中的神经元翻译组进行了分析。神经元 STAT1 信号和下游 CCL2 表达对于吞噬细胞的附着、随后的突触丧失和神经疾病是必需的。在拉姆斯登脑炎患者的大脑中也观察到了类似的现象。在这种破坏性的 CD8 T 细胞驱动的自身免疫性疾病中,神经元 STAT1 磷酸化和 CCL2 表达与浸润的 CD8 T 细胞和吞噬细胞聚集在一起。总之,我们的研究结果揭示了神经元在协调吞噬细胞介导的突触丧失中的积极作用,并强调神经元 STAT1 和 CCL2 是这一过程中的关键步骤,可通过药物干预来治疗。