Wood Smoke Extract Promotes Extracellular Matrix Remodeling in Normal Human Lung Fibroblasts.
Stephanie Recillas-RománMartha MontañoVíctor RuizJulia Pérez-RamosCarina BecerrilIliana HerreraOmar Amador-MuñozY Margarita Martínez-DomínguezCarlos RamosPublished in: International journal of toxicology (2021)
Wood smoke (WS) contains many harmful compounds, including polycyclic aromatic hydrocarbons (PAHs). WS induces inflammation in the airways and lungs and can lead to the development of various acute and chronic respiratory diseases. Pulmonary fibroblasts are the main cells involved in the remodeling of the extracellular matrix (ECM) during the WS-induced inflammatory response. Although fibroblasts remain in a low proliferation state under physiological conditions, they actively participate in ECM remodeling during the inflammatory response in pathophysiological states. Consequently, we used normal human lung fibroblasts (NHLFs) to assess the potential effects of the PAHs-containing wood smoke extract (WSE) on the growth rate, total collagen synthesis, and the expression levels of collagen I and III, matrix metalloproteinase (MMP)-1, MMP-2, MMP-9, tissue inhibitor of metalloproteinase (TIMP)-1, TIMP-2, and the transforming growth factor (TGF)-β1. We also assessed MMPs activity. The results showed that WSE induced a trimodal behavior in the growth rate curves in NHLFs; the growth rate increased with 0.5-1 % WSE and decreased with 2.5% WSE, without causing cell damage; 5-20% WSE inhibited the growth and induced cell damage. After 3 hours of exposure, 2.5% WSE induced an increase in total collagen synthesis and upregulation of TGF-β1, collagen I and III, MMP-1, TIMP-1, and TIMP-2 expression. However, MMP-2 expression was downregulated and MMP-9 was not expressed. The gelatinase activity of MMP-2 was also increased. These results suggest that WSE affects the ECM remodeling in NHLFs and indicate the potential involvement of PAHs in this process.
Keyphrases
- extracellular matrix
- polycyclic aromatic hydrocarbons
- transforming growth factor
- oxidative stress
- inflammatory response
- poor prognosis
- diabetic rats
- high glucose
- drug induced
- cell migration
- human health
- induced apoptosis
- cystic fibrosis
- cell proliferation
- cell therapy
- binding protein
- climate change
- wound healing
- intensive care unit
- risk assessment
- tissue engineering
- acute respiratory distress syndrome
- lps induced
- long non coding rna
- cell death
- cell cycle arrest
- bone marrow
- hepatitis b virus
- stress induced
- mechanical ventilation