Abstract

The inflammasome is a multiprotein complex that augments the proinflammatory response by increasing the generation and cellular release of key cytokines. Specifically, the NALP3 inflammasome requires two-step signaling, priming and activation, to be functional to release the proinflammatory cytokines IL-1β and IL-18. The priming process, through unknown mechanisms, increases the protein levels of NALP3 and pro-IL-1β in cells. Here we show that LPS increases the NALP3 protein lifespan without significantly altering steady-state mRNA in human cells. LPS exposure reduces the ubiquitin-mediated proteasomal processing of NALP3 by inducing levels of an E3 ligase component, FBXO3, which targets FBXL2. The latter is an endogenous mediator of NALP3 degradation. FBXL2 recognizes Trp-73 within NALP3 for interaction and targets Lys-689 within NALP3 for ubiquitin ligation and degradation. A unique small molecule inhibitor of FBXO3 restores FBXL2 levels, resulting in decreased NALP3 protein levels in cells and, thereby, reducing the release of IL-1β and IL-18 in human inflammatory cells after NALP3 activation. Our findings uncover NALP3 as a molecular target for FBXL2 and suggest that therapeutic targeting of the inflammasome may serve as a platform for preclinical intervention.

Highlights

  • LPS increases NALP3 levels, but the mechanisms remain unknown

  • We have demonstrated previously that an Skp-Cullin-F box (SCF) subunit, F box protein, F-box O3 (FBXO3), is a proinflammatory molecule that is activated in leukocytes by endotoxin [8]

  • BC-1215 effectively decreased LPS induction of NALP3 protein induction by 44% and reduced the secretion of IL-1␤ and IL-18 after a second stimulus, ATP (Fig. 7, I and J). These observations strongly implicate FBXO3 and F-box L2 (FBXL2) as molecular inputs to NALP3 cytokine signaling (Fig. 8). These studies demonstrate a unique mechanism whereby LPS priming prolongs the lifespan of NALP3 protein in cells

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Summary

Introduction

Results: LPS prolongs the lifespan of NALP3 protein by reducing E3 ligase (SCFFBXL2)-mediated ubiquitination. Conclusion: Proinflammatory cytokine release is reduced by a small molecule that restores cellular SCFFBXL2 levels. The priming process, through unknown mechanisms, increases the protein levels of NALP3 and pro-IL-1␤ in cells. LPS exposure reduces the ubiquitin-mediated proteasomal processing of NALP3 by inducing levels of an E3 ligase component, FBXO3, which targets FBXL2. The latter is an endogenous mediator of NALP3 degradation. A unique small molecule inhibitor of FBXO3 restores FBXL2 levels, resulting in decreased NALP3 protein levels in cells and, thereby, reducing the release of IL-1␤ and IL-18 in human inflammatory cells after NALP3 activation. Our findings uncover NALP3 as a molecular target for FBXL2 and suggest that therapeutic targeting of the inflammasome may serve as a platform for preclinical intervention

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