在活动性 EAE 模型中,脊髓 CSF 流受损先于免疫细胞浸润。

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Li Xin, Adrian Madarasz, Daniela C Ivan, Florian Weber, Simone Aleandri, Paola Luciani, Giuseppe Locatelli, Steven T Proulx
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引用次数: 0

摘要

在多发性硬化症和动物模型实验性自身免疫性脑脊髓炎(EAE)中,免疫细胞和蛋白质在蛛网膜下腔(SAS)聚集。脊髓蛛网膜下腔(SAS)的脑脊液(CSF)流动是否受到影响尚不清楚。通过将视内近红外(NIR)成像与组织病理学分析相结合,我们观察到在EAE发病前,脊髓SAS内的CSF示踪剂大量流动明显受损,这种情况一直持续到高峰期,在慢性病期间才部分恢复。脊髓CSF流动的障碍与SAS中纤维蛋白聚集的出现同时发生,但它先于免疫细胞浸润和浅表神经胶质的破坏。相反,颅脑 CSF 流向颈淋巴结的情况在病程中没有改变。我们的研究强调了脊髓CSF流的早期和持续性损害,并建议将其作为一种敏感的成像生物标志物,以反映脑膜内的病理变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impairment of spinal CSF flow precedes immune cell infiltration in an active EAE model.

Accumulation of immune cells and proteins in the subarachnoid space (SAS) is found during multiple sclerosis and in the animal model experimental autoimmune encephalomyelitis (EAE). Whether the flow of cerebrospinal fluid (CSF) along the SAS of the spinal cord is impacted is yet unknown. Combining intravital near-infrared (NIR) imaging with histopathological analyses, we observed a significantly impaired bulk flow of CSF tracers within the SAS of the spinal cord prior to EAE onset, which persisted until peak stage and was only partially recovered during chronic disease. The impairment of spinal CSF flow coincided with the appearance of fibrin aggregates in the SAS, however, it preceded immune cell infiltration and breakdown of the glia limitans superficialis. Conversely, cranial CSF efflux to cervical lymph nodes was not altered during the disease course. Our study highlights an early and persistent impairment of spinal CSF flow and suggests it as a sensitive imaging biomarker for pathological changes within the leptomeninges.

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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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