Title : NLRP3 is dispensable for d-galactosamine/lipopolysaccharide-induced acute liver failure.

Pub. Date : 2020 Dec 17

PMID : 33041005






5 Functional Relationships(s)
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1 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). Galactosamine NLR family, pyrin domain containing 3 Mus musculus
2 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). Galactosamine NLR family, pyrin domain containing 3 Mus musculus
3 This study aims to investigate the role of NLRP3 inflammasome in D-GalN/LPS-induced fatal hepatitis. Galactosamine NLR family, pyrin domain containing 3 Mus musculus
4 We found that Nlrp3-/- and WT mice showed similar mortality against a lethal dose of D-GalN/LPS treatment. Galactosamine NLR family, pyrin domain containing 3 Mus musculus
5 Besides, Nlrp3-/- mice had reduced IL-1beta levels but similar TNF-alpha, IL-6, and MCP-1 levels compared with WT mice upon D-GalN/LPS administration. Galactosamine NLR family, pyrin domain containing 3 Mus musculus