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Publication : The E3 ubiquitin ligase Pellino2 mediates priming of the NLRP3 inflammasome.

First Author  Humphries F Year  2018
Journal  Nat Commun Volume  9
Issue  1 Pages  1560
PubMed ID  29674674 Mgi Jnum  J:265431
Mgi Id  MGI:6158221 Doi  10.1038/s41467-018-03669-z
Citation  Humphries F, et al. (2018) The E3 ubiquitin ligase Pellino2 mediates priming of the NLRP3 inflammasome. Nat Commun 9(1):1560
abstractText  The NLRP3 inflammasome has an important function in inflammation by promoting the processing of pro-IL-1beta and pro-IL-18 to their mature bioactive forms, and by inducing cell death via pyroptosis. Here we show a critical function of the E3 ubiquitin ligase Pellino2 in facilitating activation of the NLRP3 inflammasome. Pellino2-deficient mice and myeloid cells have impaired activation of NLRP3 in response to toll-like receptor priming, NLRP3 stimuli and bacterial challenge. These functions of Pellino2 in the NLRP3 pathway are dependent on Pellino2 FHA and RING-like domains, with Pellino2 promoting the ubiquitination of NLRP3 during the priming phase of activation. We also identify a negative function of IRAK1 in the NLRP3 inflammasome, and describe a counter-regulatory relationship between IRAK1 and Pellino2. Our findings reveal a Pellino2-mediated regulatory signaling system that controls activation of the NLRP3 inflammasome.
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