NLRP3
LOCUS ID114548
GENE_SYMBOLNLRP3
GENE NAMENLR family, pyrin domain containing 3
SYNONYMNSAII AVP FCU MWS FCAS CIAS1 FCAS1 NALP3 C1orf7 CLR1.1 PYPAF1 AGTAVPRL
CHROMOSOME1
HOMOLOGENE ID3600
SOURCERAT
PMIDs2513683524638060
GENE SUMMARY
This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid. [provided by RefSeq, Oct 2008]

OBSERVATION
1. NF-kappa B and TXNIP mediated the ROS-induced caspase-1 and IL-1 beta activation, which are the effectors of NLRP3 inflammasome. NLRP3 gene silencing may exert a protective effect on diabetic cardiomyopath(DCM). 2. AMPK regulates oxidative metabolism and substrate selection to control both ER stress and NLRP3 inflammasome-mediated inflammation holds promise for identifying new therapies and the tailoring of current therapies for the treatment of T2D and CVD. "