|  Help  |  About  |  Contact Us

Publication : A comparative study of matrix remodeling in chronic models for COPD; mechanistic insights into the role of TNF-α.

First Author  Eurlings IM Year  2014
Journal  Am J Physiol Lung Cell Mol Physiol Volume  307
Issue  7 Pages  L557-65
PubMed ID  25106431 Mgi Jnum  J:222067
Mgi Id  MGI:5643913 Doi  10.1152/ajplung.00116.2014
Citation  Eurlings IM, et al. (2014) A comparative study of matrix remodeling in chronic models for COPD; mechanistic insights into the role of TNF-alpha. Am J Physiol Lung Cell Mol Physiol 307(7):L557-65
abstractText  Remodeling in chronic obstructive pulmonary disease (COPD) has at least two dimensions: small airway wall thickening and destruction of alveolar walls. Recently we showed comparable alterations of the extracellular matrix (ECM) compounds collagen, hyaluoran, and elastin in alveolar and small airway walls of COPD patients. The aim of this study was to characterize and assess similarities in alveolar and small airway wall matrix remodeling in chronic COPD models. From this comparative characterization of matrix remodeling we derived and elaborated underlying mechanisms to the matrix changes reported in COPD. Lung tissue sections of chronic models for COPD, either induced by exposure to cigarette smoke, chronic intratracheal lipopolysaccharide instillation, or local tumor necrosis factor (TNF) expression [surfactant protein C (SPC)-TNFalpha mice], were stained for elastin, collagen, and hyaluronan. Furthermore TNF-alpha matrix metalloproteinase (MMP)-2, -9, and -12 mRNA expression was analyzed using qPCR and localized using immunohistochemistry. Both collagen and hyaluronan were increased in alveolar and small airway walls of all three models. Interestingly, elastin contents were differentially affected, with a decrease in both alveolar and airway walls in SPC-TNFalpha mice. Furthermore TNF-alpha and MMP-2 and -9 mRNA and protein levels were found to be increased in alveolar walls and around airway walls only in SPC-TNFalpha mice. We show that only SPC-TNFalpha mice show changes in elastin remodeling that are comparable to what has been observed in COPD patients. This reveals that the SPC-TNFalpha model is a suitable model to study processes underlying matrix remodeling and in particular elastin breakdown as seen in COPD. Furthermore we indicate a possible role for MMP-2 and MMP-9 in the breakdown of elastin in airways and alveoli of SPC-TNFalpha mice.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

4 Bio Entities

0 Expression