학술논문

PAI-1 promotes extracellular matrix deposition in the airways of a murine asthma model
Document Type
Article
Source
Biochemical & Biophysical Research Communications. Jun2002, Vol. 294 Issue 5, p1155. 6p.
Subject
*PLASMINOGEN activators
*INFLAMMATION
*EXTRACELLULAR matrix
*FIBRINOLYSIS
Language
ISSN
0006-291X
Abstract
Dysregulation of matrix metalloproteinases (MMPs) and ineffective fibrinolysis are associated with the deposition of extracellular matrix (ECM). We hypothesized that elevated plasminogen activator inhibitor (PAI)-1 promotes ECM deposition in the asthmatic airway by inhibiting MMP-9 activity and fibrinolysis. Degree of airway inflammation was similar in PAI-1−/− and wild type (WT) mice after ovalbumin (OVA) challenge. PAI-1 production, deposition of collagen and fibrin, and MMP-9 activity in the lung tissue or airways were greater after OVA challenge compared with saline challenge. However, in PAI-1−/− mice, collagen deposition was 2-fold less, fibrin deposition was 4-fold less, and MMP-9 activity was 3-fold higher. This is the first direct evidence that the plasmin system regulates ECM deposition in the airways of a murine asthma model, independently of the effect of PAI-1 on inflammatory cells. The results suggest that the PAI-1-dependent inhibition of MMP-9 activity and fibrinolysis is a major mechanism by which ECM deposition occurs. [Copyright &y& Elsevier]