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Cutting Edge: NF-κB Activating Pattern Recognition and Cytokine Receptors License NLRP3 Inflammasome Activation by Regulating NLRP3 Expression
Author(s) -
Franz Bauernfeind,
Gábor Horváth,
Andrea Stutz,
Emad S. Alnemri,
Kelly L. MacDonald,
David P. Speert,
Teresa FernandesAlnemri,
Jianghong Wu,
Brian G. Monks,
Katherine A. Fitzgerald,
Veit Hornung,
Eicke Latz
Publication year - 2009
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0901363
Subject(s) - inflammasome , microbiology and biotechnology , receptor , proinflammatory cytokine , pattern recognition receptor , transcription factor , signal transduction , priming (agriculture) , extracellular , chemistry , biology , immunology , innate immune system , inflammation , biochemistry , gene , botany , germination
The IL-1 family cytokines are regulated on transcriptional and posttranscriptional levels. Pattern recognition and cytokine receptors control pro-IL-1beta transcription whereas inflammasomes regulate the proteolytic processing of pro-IL-1beta. The NLRP3 inflammasome, however, assembles in response to extracellular ATP, pore-forming toxins, or crystals only in the presence of proinflammatory stimuli. How the activation of gene transcription by signaling receptors enables NLRP3 activation remains elusive and controversial. In this study, we show that cell priming through multiple signaling receptors induces NLRP3 expression, which we identified to be a critical checkpoint for NLRP3 activation. Signals provided by NF-kappaB activators are necessary but not sufficient for NLRP3 activation, and a second stimulus such as ATP or crystal-induced damage is required for NLRP3 activation.

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