Induction and regulation of matrix metalloproteinase-12 in human airway smooth muscle cells

Publication Type:
Journal Article
Citation:
Respiratory Research, 2005, 6
Issue Date:
2005-12-16
Metrics:
Full metadata record
Files in This Item:
Filename Description Size
Thumbnail2013000350OK.pdf597.21 kB
Adobe PDF
Background: The elastolytic enzyme matrix metalloproteinase (MMP)-12 has been implicated in the development of airway inflammation and remodeling. We investigated whether human airway smooth muscle cells could express and secrete MMP-12, thereby participating in the pathogenesis of airway inflammatory diseases. Methods: Laser capture microdissection was used to collect smooth muscle cells from human bronchial biopsy sections. MMP-12 mRNA expression was analysed by quantitative real-time RT-PCR. MMP-12 protein expression and secretion from cultured primary airway smooth muscle cells was further analysed by Western blot. MMP-12 protein localization in bronchial tissue sections was detected by immunohistochemistry. MMP-12 activity was determined by zymography. The TransAM AP-1 family kit was used to measure c-Jun activation and nuclear binding. Analysis of variance was used to determine statistical significance. Results: We provide evidence that MMP-12 mRNA and protein are expressed by in situ human airway smooth muscle cells obtained from bronchial biopsies of normal volunteers, and of patient with asthma, COPD and chronic cough. The proinflammatory cytokine, interleukin (IL)-1β induced a >100-fold increase in MMP-12 gene expression and a >10-fold enhancement in MMP-12 activity of primary airway smooth muscle cell cultures. Selective inhibitors of extracellular signal-regulated kinase, c-Jun N-terminal kinase and phosphatidylinositol 3-kinase reduced the activity of IL-1β on MMP-12, indicating a role for these kinases in IL-1β-induced induction and release of MMP-12. IL-1β-induced MMP-12 activity and gene expression was down-regulated by the corticosteroid dexamethasone but up-regulated by the inflammatory cytokine tumour necrosis factor (TNF)-α through enhancing activator protein-1 activation by IL-1β.Transforming growth factor-β had no significant effect on MMP-12 induction. Conclusion: Our findings indicate that human airway smooth muscle cells express and secrete MMP-12 that is up-regulated by IL-1β and TNF-α. Bronchial smooth muscle cells may be an important source of elastolytic activity, thereby participating in remodeling in airway diseases such as COPD and chronic asthma. © 2005 Xie et al., licensee Bio Med Central Ltd.
Please use this identifier to cite or link to this item: