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  3. Impairment of spinal CSF flow precedes immune cell infiltration in an active EAE model.
 

Impairment of spinal CSF flow precedes immune cell infiltration in an active EAE model.

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BORIS DOI
10.48620/76547
Date of Publication
October 23, 2024
Publication Type
Article
Division/Institute

Theodor Kocher Instit...

Departement of Chemis...

DCBP Gruppe Prof. Luc...

Contributor
Xin, Li
Theodor Kocher Institute (TKI)
Madarasz, Adrian
Theodor Kocher Institute (TKI)
Ivan, Daniela C.
Theodor Kocher Institute (TKI)
Weber, Florian
Departement of Chemistry, Biochemistry and Pharmaceutical Sciences (DCBP), Chemistry & Biochemistry
Aleandri, Simone
DCBP Gruppe Prof. Luciani
Luciani, Paola
DCBP Gruppe Prof. Luciani
Locatelli, Giuseppe
Theodor Kocher Institute (TKI)
Proulx, Steven T.
Theodor Kocher Institute (TKI)
Subject(s)

600 - Technology::610...

500 - Science::540 - ...

Series
Journal of Neuroinflammation
ISSN or ISBN (if monograph)
1742-2094
Publisher
BioMed Central
Language
English
Publisher DOI
10.1186/s12974-024-03247-9
PubMed ID
39444001
Uncontrolled Keywords

CSF flow

Cerebrospinal fluid

Experimental autoimmu...

Glia limitans

Multiple sclerosis

Neuroinflammation

Subarachnoid space

Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/189487
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
s12974-024-03247-9.pdftextAdobe PDF15.29 MBAttribution (CC BY 4.0)publishedOpen
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