Mesoporous silica nanoparticles induced hepatotoxicity via NLRP3 inflammasome activation and caspase-1-dependent pyroptosis

• Published in: Nanoscale 2018-01, Vol.10 (19), p.9141-9152
• Main Authors: Zhang, Xuyao, Luan, Jingyun, Chen, Wei, Fan, Jiajun, Nan, Yanyang, Wang, Yichen, Liang, Yanxu, Meng, Guangxun, Ju, Dianwen
• Format: Article
• Language: English
• Subjects: Activation; Alanine; Animals; Biocompatibility; Biomedical materials; Caspase 1 - metabolism; Cell death; Cell Line; Chemical and Drug Induced Liver Injury - metabolism; Hepatocytes - cytology; Hepatocytes - drug effects; Humans; Inflammasomes - metabolism; Liver; Mice; Mice, Inbred BALB C; Mice, Knockout; Mitochondria - metabolism; Nanoparticles; Nanoparticles - toxicity; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism; Proteins; Pyroptosis; Reactive Oxygen Species - metabolism; Rodents; Silicon dioxide; Silicon Dioxide - toxicity; Time dependence; Toxicity
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/c8nr00554k

Increased biomedical applications of mesoporous silica nanoparticles (MSNs) raise considerable attention concerning their toxicological effects; the toxicities of MSNs are still undefined and the underlying mechanisms are unknown. We conducted this study to determine the hepatotoxicity of continuous administration of MSNs and the potential mechanisms. MSNs caused cytotoxicity in hepatic L02 cells in a dose- and time-dependent manner. Then, MSNs were shown to elicit NOD-like receptor protein 3 (NLRP3) inflammasome activation in hepatocytes, leading to caspase-1-dependent pyroptosis, a novel manner of cell death. In vivo MSN administration triggered hepatotoxicity as indicated by increased histological injury, serum alanine aminotransferase and serum aspartate aminotransferase. Notably, NLRP3 inflammasome and pyroptosis were also activated during the treatment. Meanwhile, in NLRP3 knockout mice and caspase-1 knockout mice, MSN-induced liver inflammation and hepatotoxicity could be abolished. Furthermore, experiments indicated that MSNs induced mitochondrial reactive oxygen species (ROS) generation, and the ROS scavenger could attenuate the MSN-activated NLRP3 inflammasomes and pyroptosis in the liver. Collectively, these data suggested that MSNs triggered liver inflammation and hepatocyte pyroptosis through NLRP3 inflammasome activation, which was caused by MSN-induced ROS generation. Our study provided novel insights into the hepatotoxicity of MSNs and the underlying mechanisms, and facilitated the potential approach to increase the biosafety of MSNs.