Inhibition of MMP-9 expression by PPAR activators in human bronchial epithelial cells
Authors:
- M HetzelMHM Hetzel
- D WalcherDWD Walcher
- M GrübMGM Grüb
- H BachHBH Bach
- V HombachVHV Hombach
- N MarxNMN Marx
Open Access
Abstract
Background: The release of matrix degrading enzymes such as matrix metalloproteinase 9 (MMP-9) from bronchial epithelial cells is critically involved in airway wall remodelling in chronic inflammatory processes of the respiratory system. MMP-9 expression is induced by inflammatory mediators such as tumour necrosis factor (TNF)-α, but to date nothing is known about the mechanisms of inhibition of MMP-9 expression in these cells. Methods: A study was undertaken to examine whether activators of the nuclear transcription factor peroxisome proliferator activated receptor gamma (PPARγ) might modulate MMP-9 expression in two different bronchial epithelial cell lines. Results: PPARγ was expressed and was functionally active in NL20 and BEAS cells. Activation of PPARγ by rosiglitazone or pioglitazone significantly reduced TNF-α and PMA induced MMP-9 gelatinolytic activity in a concentration dependent manner in both cell lines, but did not alter the expression of tissue inhibitor of MMPs type 1 (TIMP-1), the local inhibitor of MMP-9. Northern blot analysis revealed a decrease in MMP-9 mRNA expression following treatment with PPARγ which resulted from the inhibition of NF-κB activation in these cells, as determined by transient transfection assays and electromobility shift assays. Conclusion: Activation of PPARγ in human bronchial epithelial cells limits the expression of matrix degrading MMP-9. This might have therapeutic applications in chronic inflammatory processes of the respiratory system.Keywords
This publication has 24 references indexed in Scilit:
- Regulation of Peroxisome Proliferator-activated Receptor γ Expression in Human Asthmatic AirwaysAmerican Journal of Respiratory and Critical Care Medicine, 2001
- Peroxisome Proliferator-Activated Receptors (PPARs) and Their Role in the Vessel Wall: Possible Mediators of Cardiovascular Risk?European Journal of Preventive Cardiology, 2001
- PPAR-γ dependent and independent effects on macrophage-gene expression in lipid metabolism and inflammationNature Medicine, 2001
- Activation of Human Peroxisome Proliferator-Activated Receptor (PPAR) Subtypes by PioglitazoneBiochemical and Biophysical Research Communications, 2000
- Peroxisome Proliferator-Activated Receptor-γ Activators Inhibit IFN-γ-Induced Expression of the T Cell-Active CXC Chemokines IP-10, Mig, and I-TAC in Human Endothelial CellsThe Journal of Immunology, 2000
- Inhibition of Human Lung Cancer Cell Growth by the Peroxisome Proliferator-Activated Receptor-γ Agonists through Induction of ApoptosisBiochemical and Biophysical Research Communications, 2000
- Airway remodeling in asthmaJournal of Clinical Investigation, 1999
- Airway Remodeling and RepairAmerican Journal of Respiratory and Critical Care Medicine, 1999
- Immunohistochemical localisation of the matrix metalloproteinases MMP-3 and MMP-9 within the airways in asthmaThorax, 1999
- TroglitazoneDrugs, 1999