Cell death is not essential for caspase-1-mediated interleukin-1β activation and secretion

Caspase-1 cleaves and activates the pro-inflammatory cytokine interleukin-1 beta ( IL-1 beta), yet the mechanism of IL-1 beta release and its dependence on cell death remains controversial. To address this issue, we generated a novel inflammasome independent system in which we directly activate caspase-1 by dimerization. In this system, caspase-1 dimerization induced the cleavage and secretion of IL-1 beta, which did not require processing of caspase-1 into its p20 and p10 subunits. Moreover, direct caspase-1 dimerization allowed caspase-1 activation of IL-1 beta to be separated from cell death. Specifically, we demonstrate at the single cell level that IL-1 beta can be released from live, metabolically active, cells following caspase-1 activation. In addition, we show that dimerized or endogenous caspase-8 can also directly cleave IL-1 beta into its biologically active form, in the absence of canonical inflammasome components. Therefore, cell death is not obligatory for the robust secretion of bioactive IL-1 beta.