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- W4313367721 abstract "As a key component of the inflammasome, NLRP3 is a critical intracellular danger sensor emerging as an important clinical target in inflammatory diseases. However, little is known about the mechanisms that determine the kinetics of NLRP3 inflammasome stability and activity to ensure effective and controllable inflammatory responses. Here, we show that S-palmitoylation acts as a brake to turn NLRP3 inflammasome off. zDHHC12 is identified as the S-acyltransferase for NLRP3 palmitoylation, which promotes its degradation through the chaperone-mediated autophagy pathway. Zdhhc12 deficiency in mice enhances inflammatory symptoms and lethality following alum-induced peritonitis and LPS-induced endotoxic shock. Notably, several disease-associated mutations in NLRP3 are associated with defective palmitoylation, resulting in overt NLRP3 inflammasome activation. Thus, our findings identify zDHHC12 as a repressor of NLRP3 inflammasome activation and uncover a previously unknown regulatory mechanism by which the inflammasome pathway is tightly controlled by the dynamic palmitoylation of NLRP3." @default.
- W4313367721 created "2023-01-06" @default.
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- W4313367721 date "2023-01-01" @default.
- W4313367721 modified "2023-10-14" @default.
- W4313367721 title "Palmitoylation prevents sustained inflammation by limiting NLRP3 inflammasome activation through chaperone-mediated autophagy" @default.
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- W4313367721 doi "https://doi.org/10.1016/j.molcel.2022.12.002" @default.
- W4313367721 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36586411" @default.
- W4313367721 hasPublicationYear "2023" @default.
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