S100a8 inhibitor Paquinimod attenuates coal dust-induced pulmonary fibrosis via blocking neutrophils-S100a8-Tlr4-macrophages signaling axis

Int Immunopharmacol. 2025 Aug 28:161:115020. doi: 10.1016/j.intimp.2025.115020. Epub 2025 Jun 6.

Abstract

Prolonged inhalation of environmental dust leads to the onset of life-threatening pulmonary fibrosis. Identifying therapeutic targets and drugs for this disease is of critical urgency. However, traditional drug discovery often overlooks cell communication signals. Here, our single-cell omics data and in vivo experiments of the murine coal pneumoconiosis model revealed that a subpopulation of neutrophils with high expression of S100a8 enhanced the communication between neutrophils and macrophages. Based on these findings, we hypothesized that inhibiting S100a8 could mitigate coal dust-induced pulmonary fibrosis. To test this hypothesis, we employed Paquinimod, an S100a8 inhibitor. Our data demonstrated that Paquinimod alleviated coal dust-induced pulmonary fibrosis by blocking the neutrophil-S100a8-Tlr4-macrophage signaling axis, suppressing the Tlr4/p38MAPK/NF-κB pathway, lowering phosphorylation levels of p38MAPK and NF-κB p65. These inhibitions reduced inflammatory factors (TNF-α) and fibrotic markers (α-SMA, Fibronectin, TGF-β1), slowing fibrosis progression and improving lung function. Furthermore, the neutralization effect of recombinant S100a8 protein on Paquinimod's efficacy underscored the pivotal role of neutrophil-S100a8-Tlr4-macrophage communication. In conclusion, our study elucidates the critical role of S100a8 in coal dust-induced pulmonary fibrosis and highlights the potential of S100a8 inhibition by Paquinimod as a therapeutic strategy. These findings provide insight into potential treatments for pulmonary complications associated with coal pneumoconiosis.

Keywords: Murine coal pneumoconiosis model; Omics; Paquinimod; Pulmonary fibrosis; S100a8; scRNA-seq.

MeSH terms

  • Animals
  • Anthracosis* / drug therapy
  • Anthracosis* / immunology
  • Calgranulin A* / antagonists & inhibitors
  • Calgranulin A* / metabolism
  • Disease Models, Animal
  • Dust
  • Humans
  • Lung / drug effects
  • Lung / immunology
  • Lung / pathology
  • Macrophages* / drug effects
  • Macrophages* / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neutrophils* / drug effects
  • Neutrophils* / immunology
  • Pulmonary Fibrosis* / chemically induced
  • Pulmonary Fibrosis* / drug therapy
  • Pulmonary Fibrosis* / immunology
  • Signal Transduction / drug effects
  • Toll-Like Receptor 4 / metabolism

Substances

  • Toll-Like Receptor 4
  • Calgranulin A
  • Tlr4 protein, mouse
  • Dust
  • S100a8 protein, mouse