趋化因子
下调和上调
生物
脑脊液
免疫学
免疫系统
趋化因子受体
免疫失调
CD8型
细胞因子
小胶质细胞
T细胞
炎症
神经科学
基因
生物化学
作者
Natalie Piehl,Lynn van Olst,Abhirami Ramakrishnan,Victoria Teregulova,Brooke Simonton,Ziyang Zhang,Emma Tapp,Divya Channappa,Hamilton Oh,Patricia Morán Losada,Jarod Rutledge,Alexandra N. Trelle,Elizabeth C. Mormino,Fanny M. Elahi,Douglas Galasko,Victor W. Henderson,Anthony D. Wagner,Tony Wyss‐Coray,David Gate
出处
期刊:Cell
[Elsevier]
日期:2022-12-01
卷期号:185 (26): 5028-5039.e13
被引量:57
标识
DOI:10.1016/j.cell.2022.11.019
摘要
Cerebrospinal fluid (CSF) contains a tightly regulated immune system. However, knowledge is lacking about how CSF immunity is altered with aging or neurodegenerative disease. Here, we performed single-cell RNA sequencing on CSF from 45 cognitively normal subjects ranging from 54 to 82 years old. We uncovered an upregulation of lipid transport genes in monocytes with age. We then compared this cohort with 14 cognitively impaired subjects. In cognitively impaired subjects, downregulation of lipid transport genes in monocytes occurred concomitantly with altered cytokine signaling to CD8 T cells. Clonal CD8 T effector memory cells upregulated C-X-C motif chemokine receptor 6 (CXCR6) in cognitively impaired subjects. The CXCR6 ligand, C-X-C motif chemokine ligand 16 (CXCL16), was elevated in the CSF of cognitively impaired subjects, suggesting CXCL16-CXCR6 signaling as a mechanism for antigen-specific T cell entry into the brain. Cumulatively, these results reveal cerebrospinal fluid immune dysregulation during healthy brain aging and cognitive impairment.
科研通智能强力驱动
Strongly Powered by AbleSci AI