Tumor Suppressor Death-Associated Protein Kinase Is Required for Full Il-1 Beta Production
Resource
BLOOD v.117 n.3 pp.960-970
Journal
BLOOD
Journal Volume
v.117
Journal Issue
n.3
Pages
960-970
Date Issued
2011
Date
2011
Author(s)
CHUANG, YA-TING
CHOU, TING-FANG
WU, PEI- RUNG
CHEN, RUEY-HWA
LAI, MING-ZONG
LAI, MING- ZONG
Abstract
Interleukin-1 beta (IL-1 beta) is critical for inflammation and control of infection. The production of IL-1 beta depends on expression of pro-IL- 1 beta and inflammasome component induced by inflammatory stimuli, followed by assembly of inflammasome to generate caspase-1 for cleavage of pro-IL-1 beta. Here we show that tumor suppressor death- associated protein kinase (DAPK) deficiency impaired IL-1 beta production in macrophages. Generation of tumor necrosis factor-alpha in macrophages, in contrast, was not affected by DAPK knockout. Two tiers of defects in IL-1 beta generation were found in DAPK-deficient macrophages: decreased pro-IL -1 beta induction by some stimuli and reduced caspase-1 activation by all inflammatory stimuli examined. With a normal NLRP3 induction in DAPK- deficient macrophages, the diminished caspase-1 generation is attributed to impaired inflammasome assembly. There is a direct binding of DAPK to NLRP3, suggesting an involvement of DAPK in inflammasome formation. We further illustrated that the formation of NLRP3 inflammasome in situ induced by inflammatory signals was impaired by DAPK deficiency. Taken together, our results identify DAPK as a molecule required for full production of IL-1 beta and functional assembly of the NLRP3 inflammasome. In addition, DAPK knockout reduced uric acid crystal-triggered peritonitis, suggesting that DAPK may serve as a target in the treatment of IL-1 beta- associated autoinflammatory diseases.