NLRP3 is dispensable for d-galactosamine/lipopolysaccharide-induced acute liver failure.
Acute liver failure
Hepatitis
LPS
NLRP3
d-galactosamine
Journal
Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516
Informations de publication
Date de publication:
17 12 2020
17 12 2020
Historique:
received:
14
09
2020
accepted:
02
10
2020
pubmed:
13
10
2020
medline:
18
3
2021
entrez:
12
10
2020
Statut:
ppublish
Résumé
The nucleotide-binding domain and leucine-rich repeat-containing family pyrin domain containing 3 (NLRP3) inflammasome is involved in various acute and chronic liver diseases, however, it is not clear whether NLRP3 contributes to d-Galactosamine (D-GalN) plus lipopolysaccharide (LPS)-induced acute liver failure (ALF). This study aims to investigate the role of NLRP3 inflammasome in D-GalN/LPS-induced fatal hepatitis. We found that Nlrp3
Identifiants
pubmed: 33041005
pii: S0006-291X(20)31907-0
doi: 10.1016/j.bbrc.2020.10.003
pii:
doi:
Substances chimiques
Inflammasomes
0
Interleukin-1beta
0
Lipopolysaccharides
0
NLR Family, Pyrin Domain-Containing 3 Protein
0
Nlrp3 protein, mouse
0
Tumor Necrosis Factor-alpha
0
Galactosamine
7535-00-4
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1184-1190Informations de copyright
Copyright © 2020. Published by Elsevier Inc.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.