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1000 Titel
  • Cortical matrix remodeling as a hallmark of relapsing–remitting neuroinflammation in MR elastography and quantitative MRI
1000 Autor/in
  1. Silva, Rafaela V. |
  2. Morr, Anna S. |
  3. Herthum, Helge |
  4. Koch, Stefan P. |
  5. Mueller, Susanne |
  6. Batzdorf, Clara S. |
  7. Bertalan, Gergely |
  8. Meyer, Tom |
  9. Tzschätzsch, Heiko |
  10. Kühl, Anja A. |
  11. Boehm-Sturm, Philipp |
  12. Braun, Jürgen |
  13. Scheel, Michael |
  14. Paul, Friedemann |
  15. Infante-Duarte, Carmen |
  16. Sack, Ingolf |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-01-04
1000 Erschienen in
1000 Quellenangabe
  • 147(1):8
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-023-02658-x |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10766667/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>Multiple sclerosis (MS) is a chronic neuroinflammatory disease that involves both white and gray matter. Although gray matter damage is a major contributor to disability in MS patients, conventional clinical magnetic resonance imaging (MRI) fails to accurately detect gray matter pathology and establish a clear correlation with clinical symptoms. Using magnetic resonance elastography (MRE), we previously reported global brain softening in MS and experimental autoimmune encephalomyelitis (EAE). However, it needs to be established if changes of the spatiotemporal patterns of brain tissue mechanics constitute a marker of neuroinflammation. Here, we use advanced multifrequency MRE with tomoelastography postprocessing to investigate longitudinal and regional inflammation-induced tissue changes in EAE and in a small group of MS patients. Surprisingly, we found reversible softening in synchrony with the EAE disease course predominantly in the cortex of the mouse brain. This cortical softening was associated neither with a shift of tissue water compartments as quantified by T2-mapping and diffusion-weighted MRI, nor with leukocyte infiltration as seen by histopathology. Instead, cortical softening correlated with transient structural remodeling of perineuronal nets (PNNs), which involved abnormal chondroitin sulfate expression and microgliosis. These mechanisms also appear to be critical in humans with MS, where tomoelastography for the first time demonstrated marked cortical softening. Taken together, our study shows that neuroinflammation (i) critically affects the integrity of PNNs in cortical brain tissue, in a reversible process that correlates with disease disability in EAE, (ii) reduces the mechanical integrity of brain tissue rather than leading to water accumulation, and (iii) shows similar spatial patterns in humans and mice. These results raise the prospect of leveraging MRE and quantitative MRI for MS staging and monitoring treatment in affected patients.</jats:p>
1000 Sacherschließung
lokal Water [MeSH]
lokal Elasticity Imaging Techniques [MeSH]
lokal Multiple Sclerosis [MeSH]
lokal Humans [MeSH]
lokal Cerebral cortex
lokal Magnetic resonance elastography
lokal Animals [MeSH]
lokal Encephalomyelitis, Autoimmune, Experimental/diagnostic imaging [MeSH]
lokal Neuroinflammatory Diseases [MeSH]
lokal Magnetic Resonance Imaging [MeSH]
lokal Mice [MeSH]
lokal Multiple sclerosis
lokal Tomoelastography
lokal Original Paper
lokal Perineuronal nets
lokal Diffusion Magnetic Resonance Imaging [MeSH]
lokal Experimental autoimmune encephalomyelitis
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2lsdmEsIFJhZmFlbGEgVi4=|https://frl.publisso.de/adhoc/uri/TW9yciwgQW5uYSBTLg==|https://frl.publisso.de/adhoc/uri/SGVydGh1bSwgSGVsZ2U=|https://frl.publisso.de/adhoc/uri/S29jaCwgU3RlZmFuIFAu|https://frl.publisso.de/adhoc/uri/TXVlbGxlciwgU3VzYW5uZQ==|https://frl.publisso.de/adhoc/uri/QmF0emRvcmYsIENsYXJhIFMu|https://frl.publisso.de/adhoc/uri/QmVydGFsYW4sIEdlcmdlbHk=|https://frl.publisso.de/adhoc/uri/TWV5ZXIsIFRvbQ==|https://frl.publisso.de/adhoc/uri/VHpzY2jDpHR6c2NoLCBIZWlrbw==|https://frl.publisso.de/adhoc/uri/S8O8aGwsIEFuamEgQS4=|https://frl.publisso.de/adhoc/uri/Qm9laG0tU3R1cm0sIFBoaWxpcHA=|https://frl.publisso.de/adhoc/uri/QnJhdW4sIErDvHJnZW4=|https://frl.publisso.de/adhoc/uri/U2NoZWVsLCBNaWNoYWVs|https://frl.publisso.de/adhoc/uri/UGF1bCwgRnJpZWRlbWFubg==|https://frl.publisso.de/adhoc/uri/SW5mYW50ZS1EdWFydGUsIENhcm1lbg==|https://orcid.org/0000-0003-2460-1444
1000 Hinweis
  • DeepGreen-ID: 8aa91abd55d34476b65852cd8d465cfc ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Deutsche Forschungsgemeinschaft |
  2. Bundesministerium für Bildung und Forschung |
  3. Einstein Center for Neurosciences Berlin |
  4. Research Training Group GRK2260 BIOQIC |
  5. Charité – Universitätsmedizin Berlin |
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1000 Dateien
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    1000 Förderer Deutsche Forschungsgemeinschaft |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Bundesministerium für Bildung und Forschung |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Einstein Center for Neurosciences Berlin |
    1000 Förderprogramm -
    1000 Fördernummer -
  4. 1000 joinedFunding-child
    1000 Förderer Research Training Group GRK2260 BIOQIC |
    1000 Förderprogramm -
    1000 Fördernummer -
  5. 1000 joinedFunding-child
    1000 Förderer Charité – Universitätsmedizin Berlin |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 Erstellt am 2025-02-06T02:51:40.557+0100
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