Novel cell-based analysis reveals region-dependent changes in microglial dynamics in grey matter in a cuprizone model of demyelination.
Animals
CA1 Region, Hippocampal
/ metabolism
Cell Enlargement
Cell Proliferation
Cerebral Cortex
/ metabolism
Chelating Agents
/ toxicity
Cuprizone
/ toxicity
Demyelinating Diseases
/ chemically induced
Disease Models, Animal
Gray Matter
Hippocampus
/ metabolism
Imaging, Three-Dimensional
Mice
Mice, Knockout
Microglia
/ metabolism
Microscopy, Confocal
Multiple Sclerosis
/ chemically induced
Optical Imaging
Phagocytosis
Potassium Channels, Tandem Pore Domain
/ genetics
Remyelination
2-photon imaging
Brain surveillance
Cuprizone
Demyelination
MicroApp
Microglia heterogeneity
Multiple sclerosis
Journal
Neurobiology of disease
ISSN: 1095-953X
Titre abrégé: Neurobiol Dis
Pays: United States
ID NLM: 9500169
Informations de publication
Date de publication:
09 2021
09 2021
Historique:
received:
08
02
2021
revised:
25
06
2021
accepted:
13
07
2021
pubmed:
19
7
2021
medline:
5
2
2022
entrez:
18
7
2021
Statut:
ppublish
Résumé
Microglia are key players in Multiple Sclerosis (MS), expressing many susceptibility genes for this disease. They constantly survey the brain microenvironment, but the precise functional relationships between microglia and pathological processes remain unknown. We performed a detailed assessment of microglial dynamics in three distinct grey matter regions in a cuprizone-induced demyelination model. We found that microglial activation preceded detectable demyelination and showed regional specificities, such as prominent phagocytic activity in cortical layer 5 and early hypertrophic morphology in hippocampal CA1. Demyelination happened earliest in cortical layer 5, although was more complete in CA1. In cortical layer 2/3, microglial activation and demyelination were less pronounced but microglia became hyper-ramified with slower process movement during remyelination, thereby maintaining local brain surveillance. Profiling of microglia using specific morphological and motility parameters revealed region-specific heterogeneity of microglial responses in the grey matter that might serve as sensitive indicators of progression in CNS demyelinating diseases.
Identifiants
pubmed: 34274460
pii: S0969-9961(21)00198-4
doi: 10.1016/j.nbd.2021.105449
pii:
doi:
Substances chimiques
Chelating Agents
0
Kcnk13 protein, mouse
0
Potassium Channels, Tandem Pore Domain
0
Cuprizone
5N16U7E0AO
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
105449Informations de copyright
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.