Dectin-1 is an extracellular pathogen sensor for the induction and processing of IL-1β via a noncanonical caspase-8 inflammasome

SI Gringhuis, TM Kaptein, BA Wevers, B Theelen… - Nature …, 2012 - nature.com
Nature immunology, 2012nature.com
Production of the proinflammatory cytokine interleukin 1β (IL-1β) by dendritic cells is crucial
in host defense. Here we identify a previously unknown role for dectin-1 in the activation of a
noncanonical caspase-8 inflammasome in response to fungi and mycobacteria. Dectin-1
induced both the production and maturation of IL-1β through signaling routes mediated by
the kinase Syk. Whereas the CARD9–Bcl-10–MALT1 scaffold directed IL1B transcription, the
recruitment of MALT1–caspase-8 and ASC into this scaffold was crucial for processing of pro …
Abstract
Production of the proinflammatory cytokine interleukin 1β (IL-1β) by dendritic cells is crucial in host defense. Here we identify a previously unknown role for dectin-1 in the activation of a noncanonical caspase-8 inflammasome in response to fungi and mycobacteria. Dectin-1 induced both the production and maturation of IL-1β through signaling routes mediated by the kinase Syk. Whereas the CARD9–Bcl-10–MALT1 scaffold directed IL1B transcription, the recruitment of MALT1–caspase-8 and ASC into this scaffold was crucial for processing of pro-IL-1β by caspase-8. In contrast to activation of the canonical caspase-1 inflammasome, which requires additional activation of cytosolic receptors, activation of the noncanonical caspase-8 inflammasome was independent of pathogen internalization. Thus, dectin-1 acted as an extracellular sensor for pathogens that induced both IL-1β production and maturation through a noncanonical caspase-8-dependent inflammasome for protective immunity.
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