生物
星形胶质细胞
多发性硬化
流式细胞术
转录组
计算生物学
实验性自身免疫性脑脊髓炎
细胞生物学
免疫学
遗传学
基因
基因表达
中枢神经系统
神经科学
作者
Iain C. Clark,Michael A. Wheeler,Hong‐Gyun Lee,Zhaorong Li,Liliana M. Sanmarco,Shravan Thaploo,Carolina Manganeli Polonio,Seung Won Shin,Giulia Scalisi,Amy R. Henry,Joseph M. Rone,Federico Giovannoni,Marc Charabati,Camilo Faust Akl,Dulce M. Aleman,Stéphanie Zandee,Alexandre Prat,Daniel C. Douek,Eli Boritz,Francisco J. Quintana,Adam R. Abate
出处
期刊:Nature
[Springer Nature]
日期:2023-01-04
卷期号:614 (7947): 326-333
被引量:39
标识
DOI:10.1038/s41586-022-05613-0
摘要
Multiple sclerosis is a chronic inflammatory disease of the central nervous system1. Astrocytes are heterogeneous glial cells that are resident in the central nervous system and participate in the pathogenesis of multiple sclerosis and its model experimental autoimmune encephalomyelitis2,3. However, few unique surface markers are available for the isolation of astrocyte subsets, preventing their analysis and the identification of candidate therapeutic targets; these limitations are further amplified by the rarity of pathogenic astrocytes. Here, to address these challenges, we developed focused interrogation of cells by nucleic acid detection and sequencing (FIND-seq), a high-throughput microfluidic cytometry method that combines encapsulation of cells in droplets, PCR-based detection of target nucleic acids and droplet sorting to enable in-depth transcriptomic analyses of cells of interest at single-cell resolution. We applied FIND-seq to study the regulation of astrocytes characterized by the splicing-driven activation of the transcription factor XBP1, which promotes disease pathology in multiple sclerosis and experimental autoimmune encephalomyelitis4. Using FIND-seq in combination with conditional-knockout mice, in vivo CRISPR-Cas9-driven genetic perturbation studies and bulk and single-cell RNA sequencing analyses of samples from mouse experimental autoimmune encephalomyelitis and humans with multiple sclerosis, we identified a new role for the nuclear receptor NR3C2 and its corepressor NCOR2 in limiting XBP1-driven pathogenic astrocyte responses. In summary, we used FIND-seq to identify a therapeutically targetable mechanism that limits XBP1-driven pathogenic astrocyte responses. FIND-seq enables the investigation of previously inaccessible cells, including rare cell subsets defined by unique gene expression signatures or other nucleic acid markers.
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