Wood Smoke Extract Promotes Extracellular Matrix Remodeling in Normal Human Lung Fibroblasts

Author:

Recillas-Román Stephanie1,Montaño Martha2ORCID,Ruiz Víctor3,Pérez-Ramos Julia4,Becerril Carina2,Herrera Iliana5,Amador-Muñoz Omar6,Martínez-Domínguez Y. Margarita6ORCID,Ramos Carlos2ORCID

Affiliation:

1. Doctorate in Biological and Health Sciences, Metropolitan Autonomous University-Xochimilco (UAM-X), Mexico City, Mexico

2. Cell Biology Laboratory, Department of Research in Pulmonary Fibrosis, National Institute of Respiratory Diseases Ismael Cosío Villegas (INER), Mexico City, Mexico

3. Molecular Biology Laboratory, Department of Research in Pulmonary Fibrosis, National Institute of Respiratory Diseases Ismael Cosío Villegas (INER), Mexico City, Mexico

4. Department of Biological Systems, Metropolitan Autonomous University-Xochimilco (UAM-X), Mexico City, Mexico

5. Laboratory of Pulmonary Biopathology INER- Faculty of Sciences, National Autonomous University of Mexico (UNAM), Mexico; Pulmonary Fibrosis Research Department, Ismael Cosío Villegas National Institute of Respiratory Diseases (INER), Mexico City, Mexico

6. Group of Chemical Speciation of Atmospheric Organic Aerosols, Center for Atmospheric Sciences, National Autonomous University of Mexico Mexico

Abstract

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.

Publisher

SAGE Publications

Subject

Toxicology

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