Preclinical model of multiple sclerosis: Focal, chemical or viral demyelination.
Cuprizone
Demyelination
Ethidium bromide
Lysolecithin
Multiple Sclerosis
Remyelination
Theiler's Murine Encephalitis Virus
Journal
Methods in cell biology
ISSN: 0091-679X
Titre abrégé: Methods Cell Biol
Pays: United States
ID NLM: 0373334
Informations de publication
Date de publication:
2022
2022
Historique:
entrez:
3
4
2022
pubmed:
4
4
2022
medline:
6
4
2022
Statut:
ppublish
Résumé
Multiple Sclerosis (MS) is characterized by the presence of demyelinating lesions in the Central Nervous System (CNS). The demyelination is accompanied by axonal degeneration and the activation of cells of the innate and adaptive immune systems that accumulate around the demyelinated plaques. Oligodendrocyte cell dysfunction and death are also evident. In the relapsing-remitting form of MS, this dysfunction is followed by periods of recovery, and newly mature oligodendrocytes have the ability to remyelinate the pathological axons. To specifically study the localized demyelination/remyelination processes, animal models involving specific demyelinating toxins or viruses have been generated. Through these models the pathological effects on oligodendrocytes can be analyzed, and pharmacological treatments that can restore oligodendrocyte myelination capabilities can be assessed. Here we describe the most commonly used models of toxic or viral demyelination, and provide protocols to induce and analyze them.
Identifiants
pubmed: 35366993
pii: S0091-679X(21)00115-1
doi: 10.1016/bs.mcb.2021.12.010
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
87-102Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.