| First Author | Zhang W | Year | 2020 |
| Journal | Biochem Biophys Res Commun | Volume | 533 |
| Issue | 4 | Pages | 1184-1190 |
| PubMed ID | 33041005 | Mgi Jnum | J:304018 |
| Mgi Id | MGI:6693926 | Doi | 10.1016/j.bbrc.2020.10.003 |
| Citation | Zhang W, et al. (2020) NLRP3 is dispensable for d-galactosamine/lipopolysaccharide-induced acute liver failure. Biochem Biophys Res Commun 533(4):1184-1190 |
| abstractText | 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(-/-) and WT mice showed similar mortality against a lethal dose of D-GalN/LPS treatment. Serum ALT and AST levels, as well as liver necrosis area and hepatocyte apoptosis, were not significantly different between Nlrp3(-/-) and WT mice at 6 h after D-GalN/LPS injection. Moreover, the numbers of intrahepatic F4/80(+) cells and Ly6G(+) cells were comparable in two genotype mice following D-GalN/LPS treatment. 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. Our findings revealed that NLRP3 ablation does not protect mice from D-GalN/LPS-induced fatal hepatitis and has a marginal effect on intrahepatic inflammatory response upon D-GalN/LPS treatment. This suggests that NLRP3 inflammasome does not appear to be a major contributor to D-GalN/LPS-induced ALF. |
