Macrophage Extracellular Traps Suppress Particulate Matter-Induced Airway Inflammation

Am J Pathol. 2024 Sep;194(9):1622-1635. doi: 10.1016/j.ajpath.2024.05.008. Epub 2024 Jun 17.

Abstract

Accumulating evidence has substantiated the potential of ambient particulate matter (PM) to elicit detrimental health consequences in the respiratory system, notably airway inflammation. Macrophages, a pivotal component of the innate immune system, assume a crucial function in responding to exogenous agents. However, the roles and detailed mechanisms in regulating PM-induced airway inflammation remain unclear. The current study revealed that PM had the ability to stimulate the formation of macrophage extracellular traps (METs) both in vitro and in vivo. This effect was dependent on peptidylarginine deiminase type 4 (PAD4)-mediated histone citrullination. Additionally, reactive oxygen species were involved in the formation of PM-induced METs, in parallel with PAD4. Genetic deletion of PAD4 in macrophages resulted in an up-regulation of inflammatory cytokine expression. Moreover, mice with PAD4-specific knockout in myeloid cells exhibited exacerbated PM-induced airway inflammation. Mechanistically, inhibition of METs suppressed the phagocytic ability in macrophages, leading to airway epithelial injuries and an aggravated PM-induced airway inflammation. The present study demonstrates that METs play a crucial role in promoting the phagocytosis and clearance of PM by macrophages, thereby suppressing airway inflammation. Furthermore, it suggests that activation of METs may represent a novel therapeutic strategy for PM-related airway disorders.

MeSH terms

  • Animals
  • Citrullination
  • Extracellular Traps* / metabolism
  • Inflammation / metabolism
  • Inflammation / pathology
  • Macrophages* / metabolism
  • Macrophages* / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Particulate Matter* / adverse effects
  • Phagocytosis
  • Protein-Arginine Deiminase Type 4* / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Particulate Matter
  • Protein-Arginine Deiminase Type 4
  • peptidylarginine deiminase 4, mouse
  • Reactive Oxygen Species