Blockade of neutrophil extracellular trap components ameliorates cholestatic liver disease in Mdr2 (Abcb4) knockout mice.
Autoimmune liver disease
Hepatobiliary disease
Mdr2 (Abcb4) knockout mouse
Neutrophil elastase
Neutrophil extracellular trap
Journal
Journal of autoimmunity
ISSN: 1095-9157
Titre abrégé: J Autoimmun
Pays: England
ID NLM: 8812164
Informations de publication
Date de publication:
22 Apr 2024
22 Apr 2024
Historique:
received:
27
12
2023
revised:
21
03
2024
accepted:
09
04
2024
medline:
24
4
2024
pubmed:
24
4
2024
entrez:
23
4
2024
Statut:
aheadofprint
Résumé
Primary sclerosing cholangitis (PSC) is an (auto)immune-mediated cholestatic liver disease with a yet unclear etiology. Increasing evidence points to an involvement of neutrophils in chronic liver inflammation and cirrhosis but also liver repair. Here, we investigate the role of the neutrophil extracellular trap (NET) component myeloperoxidase (MPO) and the therapeutic potential of DNase I and of neutrophil elastase (NE) inhibitor GW311616A on disease outcome in the multidrug resistance 2 knockout (Mdr2
Identifiants
pubmed: 38653165
pii: S0896-8411(24)00063-5
doi: 10.1016/j.jaut.2024.103229
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
103229Informations de copyright
Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.