Ontology highlight
ABSTRACT:
SUBMITTER: Hara H
PROVIDER: S-EPMC6294477 | biostudies-literature | 2018 Nov
REPOSITORIES: biostudies-literature
Hara Hideki H Seregin Sergey S SS Yang Dahai D Fukase Koichi K Chamaillard Mathias M Alnemri Emad S ES Inohara Naohiro N Chen Grace Y GY Núñez Gabriel G
Cell 20181101 6
The activator and composition of the NLRP6 inflammasome remain poorly understood. We find that lipoteichoic acid (LTA), a molecule produced by Gram-positive bacteria, binds and activates NLRP6. In response to cytosolic LTA or infection with Listeria monocytogenes, NLRP6 recruited caspase-11 and caspase-1 via the adaptor ASC. NLRP6 activation by LTA induced processing of caspase-11, which promoted caspase-1 activation and interleukin-1β (IL-1β)/IL-18 maturation in macrophages. Nlrp6<sup>-/-</sup> ...[more]