期刊
ONCOTARGET
卷 8, 期 25, 页码 40817-40831出版社
IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.17256
关键词
autophagy; macrophage; NLRP3 inflammasome; p62/SQSTM1; rapamycin
资金
- Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI)
- Ministry of Health & Welfare, Republic of Korea [HI15C3134]
Excessive and prolonged activation of macrophages underlies many inflammatory and autoimmune diseases. To regulate activation and maintain homeostasis, macrophages have multiple intrinsic mechanisms, one of which is modulation through autophagy. Here we demonstrate that autophagy induction by rapamycin suppressed the production of IL-1 beta and IL-18 in lipopolysaccharide-and adenosine triphosphate-activated macrophages at the post-transcriptional level by eliminating mitochondrial ROS (mtROS) and pro-IL1 beta in a p62/SQSTM1-dependent manner. In addition, rapamycin activated Nrf2 through up-regulation of p62/SQSTM1, which further contributed to the reduction of mtROS. Reduced IL-1 beta subsequently diminished the activation of p38 MAPK-NF kappa B pathways, leading to transcriptional down-regulation of IL-6, IL-8, MCP-1, and I kappa B alpha in rapamycin-treated macrophages. Therefore, our results suggest that rapamycin negatively regulates macrophage activation by restricting a feedback loop of NLRP3 inflammasome-p38 MAPK-NF kappa B pathways in autophagy-and p62/SQSTM1-dependent manners.
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