Zhang Le, Yasumizu Yoshiaki, Deerhake M Elizabeth, Moon Jeonghyeon, Buitrago-Pocasangre Nicholas, Russo Anthony, Wang Haowei, Zhu Biqing, Seibyl John P, Reddy Vijaya, Wang Qianchang, Spillantini Maria Grazia, Posner David A, Clatworthy Menna, Sumida Tomokazu S, Longbrake Erin E, Cedarbaum Jesse M, Hafler David A
Department of Neurology, Yale School of Medicine, New Haven, CT, 06510, USA.
Department of Neuroscience, Yale School of Medicine, New Haven, CT, 06510, USA.
bioRxiv. 2025 May 21:2025.05.16.654530. doi: 10.1101/2025.05.16.654530.
We investigated the role of inflammation in the pathogenesis of prodromal Parkinson's Disease (PD), performing single-cell RNAseq analysis of cerebrospinal fluid (CSF) and blood from 111 individuals, comparing control subjects with early prodromal PD and later PD to patients with multiple sclerosis (MS). Surprisingly, we identified a pleocytosis in the CSF, most pronounced in patients with early PD. Single-cell RNAseq revealed increases in CSF-specific microglia-like macrophages expressing JAK-STAT and TNFα signaling signatures in prodromal PD, with a lack of T cell activation in the CSF. The CSF macrophages exhibited similar transcriptional profiles to dural macrophages from human α-synuclein-expressing PD model mice. These findings uncover a myeloid-mediated TNFα inflammatory process in the CNS of patients with prodromal PD, suggesting a novel pathological mechanism in disease etiology.
我们研究了炎症在前驱期帕金森病(PD)发病机制中的作用,对111名个体的脑脊液(CSF)和血液进行了单细胞RNA测序分析,将对照受试者、早期前驱期PD和晚期PD患者与多发性硬化症(MS)患者进行比较。令人惊讶的是,我们在脑脊液中发现了细胞增多,在早期PD患者中最为明显。单细胞RNA测序显示,在前驱期PD患者中,表达JAK-STAT和TNFα信号特征的脑脊液特异性小胶质细胞样巨噬细胞增加,而脑脊液中缺乏T细胞激活。脑脊液巨噬细胞表现出与表达人α-突触核蛋白的PD模型小鼠硬脑膜巨噬细胞相似的转录谱。这些发现揭示了前驱期PD患者中枢神经系统中髓系介导的TNFα炎症过程,提示了疾病病因学中的一种新的病理机制。