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Rapamycin regulates macrophage activation by inhibiting NLRP3 inflammasome-p38 MAPK-NF?B pathways in autophagy- and p62-dependent manners.


ABSTRACT: 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? and IL-18 in lipopolysaccharide- and adenosine triphosphate-activated macrophages at the post-transcriptional level by eliminating mitochondrial ROS (mtROS) and pro-IL1? 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? subsequently diminished the activation of p38 MAPK-NF?B pathways, leading to transcriptional down-regulation of IL-6, IL-8, MCP-1, and I?B? 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?B pathways in autophagy- and p62/SQSTM1-dependent manners.

SUBMITTER: Ko JH 

PROVIDER: S-EPMC5522223 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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Rapamycin regulates macrophage activation by inhibiting NLRP3 inflammasome-p38 MAPK-NFκB pathways in autophagy- and p62-dependent manners.

Ko Jung Hwa JH   Yoon Sun-Ok SO   Lee Hyun Ju HJ   Oh Joo Youn JY  

Oncotarget 20170601 25


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-1β and IL-18 in lipopolysaccharide- and adenosine triphosphate-activated macrophages at the post-transcriptional level by eliminating mitochondrial ROS (mtROS) and  ...[more]

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