CYBB/NOX2 in conventional DCs controls T cell encephalitogenicity during neuroinflammation.
Animals
Autophagy
/ physiology
Dendritic Cells
/ metabolism
Encephalomyelitis, Autoimmune, Experimental
/ immunology
Inflammation
/ metabolism
Lymphocyte Activation
/ immunology
Macrophages
/ metabolism
Myelin-Oligodendrocyte Glycoprotein
/ immunology
NADPH Oxidase 2
/ metabolism
Phagocytosis
/ immunology
T-Lymphocytes
/ metabolism
Antigen presentation
CYBB/NOX2
LC3-associated phagocytosis
autophagy
dendritic cells
experimental autoimmune encephalomyelitis
multiple sclerosis
Journal
Autophagy
ISSN: 1554-8635
Titre abrégé: Autophagy
Pays: United States
ID NLM: 101265188
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
pubmed:
14
5
2020
medline:
15
12
2021
entrez:
14
5
2020
Statut:
ppublish
Résumé
Whereas central nervous system (CNS) homeostasis is highly dependent on tissue surveillance by immune cells, dysregulated entry of leukocytes during autoimmune neuroinflammation causes severe immunopathology and neurological deficits. To invade the CNS parenchyma, encephalitogenic T helper (T
Identifiants
pubmed: 32401602
doi: 10.1080/15548627.2020.1756678
pmc: PMC8143233
doi:
Substances chimiques
Myelin-Oligodendrocyte Glycoprotein
0
Cybb protein, mouse
EC 1.6.3.-
NADPH Oxidase 2
EC 1.6.3.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1244-1258Subventions
Organisme : British Heart Foundation
ID : CH/1999001/11735
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/13/11/30384
Pays : United Kingdom
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