PGAM5 Modulates Macrophage Polarization, Aggravating Inflammation in COPD via the NF-κB Pathway

Int J Chron Obstruct Pulmon Dis. 2025 Mar 6:20:551-564. doi: 10.2147/COPD.S492627. eCollection 2025.

Abstract

Background: Chronic obstructive pulmonary disease (COPD) has emerged as a very consequential issue threatening human life and health; therefore, research on its pathogenesis is urgently needed. A prior investigation discovered a significant elevation in the phosphoglycerate mutase 5 (PGAM5) expression in the lung tissue of COPD smoking patients. This rise in expression is closely associated with COPD severity. Nevertheless, the precise molecular processes by which PGAM5 influences the COPD initiation and advancement remain unknown.

Materials and methods: A COPD model was created using murine alveolar macrophages (MH-S). Flow cytometry, enzyme-linked immunosorbent assay, Western blotting, and other methods were used to detect macrophage polarization, inflammatory factor secretion levels, and changes in PGAM5 and the nuclear factor-κB (NF-κB) pathway.

Results: PGAM5 stimulated macrophage M1 polarization and secretion of the proinflammatory factors interleukin-1β (IL-1β) and tumor necrosis factor-alpha (TNF-α). PGAM5 bound and activated apoptotic signaling-regulated kinase 1 (ASK1), further activating the NF-κB pathway. These implications were reversed when PGAM5 expression was silenced.

Conclusion: PGAM5 can cause an increase in p-ASK1T838, trigger the NF-κB pathway activation, and stimulate the M1 macrophage polarization and production of proinflammatory factors. This finding has significant implications for preventing and treating COPD.

Keywords: COPD; NF-κB pathway; apoptosis signal-regulating kinase 1; macrophage polarization; phosphoglycerate mutase 5.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Polarity
  • Disease Models, Animal
  • Inflammation Mediators / metabolism
  • Interleukin-1beta / metabolism
  • Lung* / enzymology
  • Lung* / pathology
  • Macrophage Activation*
  • Macrophages, Alveolar* / enzymology
  • Macrophages, Alveolar* / immunology
  • Macrophages, Alveolar* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NF-kappa B* / metabolism
  • Phenotype
  • Phosphoglycerate Mutase* / genetics
  • Phosphoglycerate Mutase* / metabolism
  • Pulmonary Disease, Chronic Obstructive* / enzymology
  • Pulmonary Disease, Chronic Obstructive* / genetics
  • Pulmonary Disease, Chronic Obstructive* / immunology
  • Pulmonary Disease, Chronic Obstructive* / pathology
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • NF-kappa B
  • Phosphoglycerate Mutase
  • Inflammation Mediators
  • Interleukin-1beta
  • Tumor Necrosis Factor-alpha
  • IL1B protein, mouse