Microglia-mediated demyelination protects against CD8


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
30 10 2023
Historique:
received: 27 01 2023
accepted: 16 10 2023
medline: 2 11 2023
pubmed: 31 10 2023
entrez: 31 10 2023
Statut: epublish

Résumé

Axon degeneration and functional decline in myelin diseases are often attributed to loss of myelin but their relation is not fully understood. Perturbed myelinating glia can instigate chronic neuroinflammation and contribute to demyelination and axonal damage. Here we study mice with distinct defects in the proteolipid protein 1 gene that develop axonal damage which is driven by cytotoxic T cells targeting myelinating oligodendrocytes. We show that persistent ensheathment with perturbed myelin poses a risk for axon degeneration, neuron loss, and behavioral decline. We demonstrate that CD8

Identifiants

pubmed: 37903797
doi: 10.1038/s41467-023-42570-2
pii: 10.1038/s41467-023-42570-2
pmc: PMC10616105
doi:

Substances chimiques

Plp1 protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6911

Informations de copyright

© 2023. The Author(s).

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Auteurs

Janos Groh (J)

Department of Neurology, Section of Developmental Neurobiology, University Hospital Würzburg, Würzburg, Germany. janos.groh@tum.de.
Institute of Neuronal Cell Biology, Technical University Munich, Munich, Germany. janos.groh@tum.de.

Tassnim Abdelwahab (T)

Department of Neurology, Section of Developmental Neurobiology, University Hospital Würzburg, Würzburg, Germany.

Yogita Kattimani (Y)

Department of Neurology, Section of Developmental Neurobiology, University Hospital Würzburg, Würzburg, Germany.

Michaela Hörner (M)

Department of Neurology, Section of Developmental Neurobiology, University Hospital Würzburg, Würzburg, Germany.
Department of Neurology, Section of Neurodegeneration, University Hospital Heidelberg, Heidelberg, Germany.

Silke Loserth (S)

Department of Neurology, Section of Developmental Neurobiology, University Hospital Würzburg, Würzburg, Germany.

Viktoria Gudi (V)

Department of Neurology, Hannover Medical School, Hannover, Germany.

Robert Adalbert (R)

John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, UK.
Department of Anatomy, Histology and Embryology, University of Szeged, Szeged, Hungary.
Institute of Health Sciences Education, Faculty of Medicine and Dentistry, Queen Mary University of London, London, UK.

Fabian Imdahl (F)

Helmholtz Institute for RNA-based Infection Research, Helmholtz-Center for Infection Research, Würzburg, Germany.

Antoine-Emmanuel Saliba (AE)

Helmholtz Institute for RNA-based Infection Research, Helmholtz-Center for Infection Research, Würzburg, Germany.
Institute of Molecular Infection Biology (IMIB), University of Würzburg, Würzburg, Germany.

Michael Coleman (M)

John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, UK.

Martin Stangel (M)

Department of Neurology, Hannover Medical School, Hannover, Germany.
Translational Medicine, Novartis Institute of Biomedical Research, Basel, Switzerland.

Mikael Simons (M)

Institute of Neuronal Cell Biology, Technical University Munich, Munich, Germany.
German Center for Neurodegenerative Diseases, Munich, Germany.
Munich Cluster of Systems Neurology, Munich, Germany.

Rudolf Martini (R)

Department of Neurology, Section of Developmental Neurobiology, University Hospital Würzburg, Würzburg, Germany. rudolf.martini@mail.uni-wuerzburg.de.

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