神经退行性变
细胞生物学
趋化因子
CX3CR1型
生物
路易体
趋化因子受体
医学
T细胞
受体
疾病
神经科学
免疫系统
病理
帕金森病
共核细胞病
化学
痴呆
α-突触核蛋白
免疫学
遗传学
作者
David Gate,Emma Tapp,Olivia Leventhal,Marian Shahid,Tim J. Nonninger,Andrew C. Yang,Katharina Strempfl,Michael S. Unger,Tobias Fehlmann,Hamilton Oh,Divya Channappa,Victor W. Henderson,Andreas Keller,Ludwig Aigner,Douglas Galasko,Mark M. Davis,Kathleen L. Poston,Tony Wyss‐Coray
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-10-14
卷期号:374 (6569): 868-874
被引量:154
标识
DOI:10.1126/science.abf7266
摘要
Recent studies indicate that the adaptive immune system plays a role in Lewy body dementia (LBD). However, the mechanism regulating T cell brain homing in LBD is unknown. Here, we observed T cells adjacent to Lewy bodies and dopaminergic neurons in postmortem LBD brains. Single-cell RNA sequencing of cerebrospinal fluid (CSF) identified up-regulated expression of C-X-C motif chemokine receptor 4 (CXCR4) in CD4+ T cells in LBD. CSF protein levels of the CXCR4 ligand, C-X-C motif chemokine ligand 12 (CXCL12), were associated with neuroaxonal damage in LBD. Furthermore, we observed clonal expansion and up-regulated interleukin 17A expression by CD4+ T cells stimulated with a phosphorylated α-synuclein epitope. Thus, CXCR4-CXCL12 signaling may represent a mechanistic target for inhibiting pathological interleukin-17–producing T cell trafficking in LBD.
科研通智能强力驱动
Strongly Powered by AbleSci AI