Dataset Information


Histones activate the NLRP3 inflammasome in Kupffer cells during sterile inflammatory liver injury.

ABSTRACT: Cellular processes that drive sterile inflammatory injury after hepatic ischemia/reperfusion (I/R) injury are not completely understood. Activation of the inflammasome plays a key role in response to invading intracellular pathogens, but mounting evidence suggests that it also plays a role in inflammation driven by endogenous danger-associate molecular pattern molecules released after ischemic injury. The nucleotide-binding domain, leucine-rich repeat containing protein 3 (NLRP3) inflammasome is one such process, and the mechanism by which its activation results in damage and inflammatory responses following liver I/R is unknown. In this article, we report that both NLRP3 and its downstream target caspase-1 are activated during I/R and are essential for hepatic I/R injury, because both NLRP3 and caspase-1 knockout mice are protected from injury. Furthermore, inflammasome-mediated injury is dependent on caspase-1 expression in liver nonparenchymal cells. Although upstream signals that activate the inflammasome during ischemic injury are not well characterized, we show that endogenous extracellular histones activate the NLRP3 inflammasome during liver I/R through TLR9. This occurs through TLR9-dependent generation of reactive oxygen species. This mechanism is operant in resident liver Kupffer cells, which drive innate immune responses after I/R injury by recruiting additional cell types, including neutrophils and inflammatory monocytes. These novel findings illustrate a new mechanism by which extracellular histones and activation of NLRP3 inflammasome contribute to liver damage and the activation of innate immunity during sterile inflammation.

PROVIDER: S-EPMC3777242 | BioStudies |

REPOSITORIES: biostudies

Similar Datasets

1000-01-01 | S-EPMC2631294 | BioStudies
| S-EPMC5074868 | BioStudies
2011-01-01 | S-EPMC3129497 | BioStudies
2011-01-01 | S-EPMC3213322 | BioStudies
1000-01-01 | S-EPMC5356637 | BioStudies
1000-01-01 | S-EPMC5947144 | BioStudies
1000-01-01 | S-EPMC4650444 | BioStudies
2020-01-01 | S-EPMC7004066 | BioStudies
2018-01-01 | S-EPMC5902503 | BioStudies
2019-01-01 | S-EPMC7016608 | BioStudies