Pyrroloquinoline quinone ameliorates PM2.5-induced pulmonary fibrosis through targeting epithelial-mesenchymal transition.
Chia-Chia ChaoSheng-Yen HsiaoWan-Chen KaoPei-Chen ChiouChieh-Chen HuangMei-Ting WangPo-Chun ChenPublished in: Journal of cellular and molecular medicine (2024)
Pulmonary fibrosis is a lung disorder affecting the lungs that involves the overexpressed extracellular matrix, scarring and stiffening of tissue. The repair of lung tissue after injury relies heavily on Type II alveolar epithelial cells (AEII), and repeated damage to these cells is a crucial factor in the development of pulmonary fibrosis. Studies have demonstrated that chronic exposure to PM2.5, a form of air pollution, leads to an increase in the incidence and severity of pulmonary fibrosis by stimulation of epithelial-mesenchymal transition (EMT) in lung epithelial cells. Pyrroloquinoline quinone (PQQ) is a bioactive compound found naturally that exhibits potent anti-inflammatory and anti-oxidative properties. The mechanism by which PQQ prevents pulmonary fibrosis caused by exposure to PM2.5 through EMT has not been thoroughly discussed until now. In the current study, we discovered that PQQ successfully prevented PM2.5-induced pulmonary fibrosis by targeting EMT. The results indicated that PQQ was able to inhibit the expression of type I collagen, a well-known fibrosis marker, in AEII cells subjected to long-term PM2.5 exposure. We also found the alterations of cellular structure and EMT marker expression in AEII cells with PM2.5 incubation, which were reduced by PQQ treatment. Furthermore, prolonged exposure to PM2.5 considerably reduced cell migratory ability, but PQQ treatment helped in reducing it. In vivo animal experiments indicated that PQQ could reduce EMT markers and enhance pulmonary function. Overall, these results imply that PQQ might be useful in clinical settings to prevent pulmonary fibrosis.
Keyphrases
- pulmonary fibrosis
- epithelial mesenchymal transition
- air pollution
- particulate matter
- induced apoptosis
- polycyclic aromatic hydrocarbons
- signaling pathway
- transforming growth factor
- heavy metals
- cell cycle arrest
- extracellular matrix
- lung function
- water soluble
- oxidative stress
- stem cells
- high glucose
- mesenchymal stem cells
- diabetic rats
- single cell
- risk factors
- cystic fibrosis
- cancer therapy
- combination therapy
- replacement therapy
- drug delivery
- binding protein