Diverse Activators Of The Nlrp3 Inflammasome Promote Il-1 Beta Secretion By Triggering Necrosis

The NLRP3 inflammasome is involved in caspase-1-dependent maturation of IL-1 beta in many contexts. A two-signal model has emerged for IL-1 beta maturation, with LPS providing "signal I'' and diverse agents such as ATP, Nigericin, streptolysin O, uric acid crystals, and alum salts capable of acting as "signal II.'' In the absence of signal II, pro-IL-1 beta is upregulated but typically fails to be processed or released. What unites signal II stimuli has been debated, with the ability to promote K+ efflux suggested as a common factor, but the mechanism of IL-1 beta release remains unclear. Here, we show that all examined inflammasome signal II agents triggered necrosis, which was highly correlated with their ability to promote IL-1 beta release. IL-1 beta secretion occurred in tandem with the release of many additional proteins and was confined to necrotic cells. Thus, signal II agents initiate inflammation by promoting necrosis-driven IL-1 beta release, suggesting that IL-1 beta represents an inducible danger signal.