Heterozygous SOD2 deletion deteriorated chronic intermittent hypoxia-induced lung inflammation and vascular remodeling through mtROS-NLRP3 signaling pathway

Acta Pharmacol Sin. 2020 Sep;41(9):1197-1207. doi: 10.1038/s41401-019-0349-y. Epub 2020 Feb 17.

Abstract

Oxidative stress caused by chronic intermittent hypoxia (CIH) is the hallmark of obstructive sleep apnea (OSA). Among the first line of defense against oxidative stress is the dismutation of superoxide radicals, which in the mitochondria is carried out by manganese superoxide dismutase (SOD2). In this study, wild-type (WT) and SOD2-heterozygous knockout (SOD2+/-) mice were exposed to CIH or normoxic (Nor) conditions. After 4 weeks, pulmonary artery pressure was measured, and the mice were processed to harvest either serum for cytokine assays or lungs for flow cytometry and histopathological studies. Herein, we showed that heterozygous deletion of SOD2 markedly deteriorated pulmonary remodeling and increased the oxidative stress, especially promoted the infiltration of macrophages in the lungs of CIH mouse. Moreover, in the intermittent hypoxia (IH)-treated RAW264.7 cells, SOD2 knockdown increased the nucleotide-binding domain-like receptor protein 3 (NLRP3) inflammasome activation accompanied with the IL-1β elevation and caspase-1 activity. Additionally, mitochondrial ROS (mtROS) scavenger mito-TEMPO abolished NLRP3 inflammasome activation in IH-treated RAW264.7 cells. Collectively, our results supported that SOD2 contributed to the pathogenesis of CIH-induced lung remodeling. Meanwhile, SOD2 knockdown exacerbates oxidative damage through assembly and activation of NLRP3 inflammasome in macrophages. SOD2 may be a novel therapeutic target for CIH-induced pulmonary inflammation and arteriole remodeling.

Keywords: NLRP3; SOD2; inflammation; intermittent hypoxia; macrophage.

MeSH terms

  • Animals
  • Gene Deletion
  • Humans
  • Hypoxia / complications*
  • Inflammasomes / metabolism
  • Inflammation / epidemiology
  • Inflammation / genetics
  • Inflammation / metabolism*
  • Lung
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitochondria / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism*
  • Oxidative Stress / genetics
  • RAW 264.7 Cells
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / physiology*
  • Sleep Apnea, Obstructive / metabolism
  • Superoxide Dismutase / deficiency*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Vascular Remodeling / genetics
  • Vascular Remodeling / physiology*

Substances

  • Inflammasomes
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Nlrp3 protein, mouse
  • Reactive Oxygen Species
  • Superoxide Dismutase
  • superoxide dismutase 2