Journal Article

DZNE-2025-00121

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png MRI-based morphometric structural changes correlate with histopathology in experimental autoimmune encephalomyelitis.

Lowinski, A. ; Dabringhaus, A. ; Kraemer, M. ; Doshi, H.DZNE* ; Weier, A. ; Hintze, M. ; Chunder, R. ; Kuerten, S.

2025
Elsevier Science Amsterdam [u.a.]

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Please use a persistent id in citations: doi:10.1016/j.jns.2024.123358

Abstract: Magnetic resonance imaging (MRI) and neurohistopathology are important correlates for evaluation of disease progression in multiple sclerosis (MS). Here we used experimental autoimmune encephalomyelitis (EAE) as an animal model of MS to determine the correlation between clinical EAE severity, MRI and histopathological parameters.N = 11 female C57BL/6J mice were immunized with human myelin oligodendrocyte glycoprotein 1-125, while N = 9 remained non-immunized. Mice were scanned longitudinally over a period of 13 weeks using a 11.7 Tesla (T) Bruker BioSpec® preclinical MRI instrument, and regional volume changes of the lumbar spinal cord were analyzed using Voxel-Guided Morphometry (VGM). Following the final in vivo T1-weighted MRI scan, the lumbar spinal cord of each mouse was subjected to an ex vivo MRI scan using T1-, T2*- and diffusion tensor imaging (DTI)-weighted sequences. Tissue sections were then stained for immune cell infiltration, demyelination, astrogliosis, and axonal damage using hematoxylin-eosin staining and immunohistochemistry.While in vivo MRI VGM detected an overall increase in volume over time, no differences were observed between EAE animals and controls. Ex vivo MRI showed a generalized atrophy of the spinal cord, which was pronounced in the anterolateral tract. The most striking correlation was observed between EAE score, white matter atrophy in ex vivo T1-weighted scans and histological parameters.The data demonstrate that ex vivo MRI is a valuable tool to assess white matter atrophy in EAE, which was shown to be directly linked to the severity of EAE and spinal cord histopathology.

Keyword(s): Encephalomyelitis, Autoimmune, Experimental: pathology (MeSH) ; Encephalomyelitis, Autoimmune, Experimental: diagnostic imaging (MeSH) ; Animals (MeSH) ; Female (MeSH) ; Mice, Inbred C57BL (MeSH) ; Magnetic Resonance Imaging: methods (MeSH) ; Spinal Cord: pathology (MeSH) ; Spinal Cord: diagnostic imaging (MeSH) ; Mice (MeSH) ; Disease Models, Animal (MeSH) ; Myelin-Oligodendrocyte Glycoprotein: immunology (MeSH) ; Diffusion Tensor Imaging: methods (MeSH) ; Experimental autoimmune encephalomyelitis ; Magnetic resonance imaging ; Multiple sclerosis ; T1 ; T2 ; T2* ; Voxel-guided morphometry ; Myelin-Oligodendrocyte Glycoprotein

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Contributing Institute(s):

1. Small Animal MRI (CRFS-SAMRI) (SAMRI)
2. Core Research Facilities & Services (CRFS)

Research Program(s):

1. 899 - ohne Topic (POF4-899) (POF4-899)

Appears in the scientific report 2025

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Database coverage:
; ; ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF < 5 ; JCR ; Nationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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