Altered Balance Between Extracellular Proteolysis and Antiproteolysis is Associated with Adaptive Coronary Arteriogenesis

• Published in: Journal of molecular and cellular cardiology 2000-06, Vol.32 (6), p.997-1011
• Main Authors: Cai, Wei-jun, Vosschulte, Regina, Afsah-Hedjri, Abdollah, Koltai, Sophie, Kocsis, Elisabeth, Scholz, Dimitri, Kostin, Sawa, Schaper, Wolfgang, Schaper, Jutta
• Format: Article
• Language: English
• Subjects: Adaptation, Physiological; Animals; Arteriogenesis; Collateral Circulation; Collateral vessel growth; Coronary Disease - metabolism; Coronary Disease - pathology; Coronary Vessels - metabolism; Coronary Vessels - pathology; Dog; Dogs; Electrophoresis, Polyacrylamide Gel - methods; Endopeptidases - metabolism; Extracellular matrix; Extracellular Space - metabolism; Fibroblast Growth Factor 2 - metabolism; Humans; Matrix Metalloproteinase 2 - metabolism; Matrix Metalloproteinase 9 - metabolism; Neovascularization, Pathologic; Rabbits; Sodium Dodecyl Sulfate; Tissue Inhibitor of Metalloproteinase-1 - metabolism; Tissue Inhibitor of Metalloproteinase-2 - metabolism; Vascular remodeling, Metalloproteinases
• ISSN: 0022-2828; 1095-8584
• DOI: 10.1006/jmcc.2000.1137

W-j. Cai, R. Vosschulte, A. Afsah-Hedjri, S. Koltai, E. Kocsis, D. Scholz, S. Kostin, W. Schaper and J. Schaper. Altered Balance Between Extracellular Proteolysis and Antiproteolysis is Associated with Adaptive Coronary Arteriogenesis.Journal of Molecular and Cellular Cardiology (2000) 32, 997–1011. To study the role of extracellular proteolysis and antiproteolysis during adaptive arteriogenesis (collateral vessel growth) we took 58 collaterals at various developmental stages from 14 dogs with chronic occlusion of the left circumflex coronary artery (LCx) by ameroid constrictor. Immunofluorescence and quantitative immunofluorescence with antibodies against α -smooth muscle actin, desmin, matrix metalloproteinases 2 (MMP-2), MMP-9, tissue inhibitor of metalloproteinases 1 (TIMP-1) and 2 (TIMP-2), urokinase-type plasminogen activator (u-PA) and its inhibitor-1 (PAI-1) were studied with confocal microscopy. Additionally, SDS-PAGE zymography was employed. We found that in normal coronary arteries, MMP-2, MMP-9 and PAI-1 were present in all layers of the wall in small amounts. TIMP-1 was found only in smooth muscle cells. In contrast, in growing collaterals, MMP-2 and MMP-9 were 3.4-fold and 4.1-fold higher in the neointima than in the media respectively. TIMP-1 was 4.4-fold higher in the media over the growing neointima. Zymography showed MMP-2 and MMP-9 activated. PAI-1 was increased, especially in the growing neointima where it was 1.4-fold higher. In mature collaterals, MMP-2 and MMP-9 were downregulated in the neointima, 1.4-fold and 1.3-fold higher over the media. TIMP-1 was 1.4-fold increased in the neointima but PAI-1 was downregulated. Desmin and α -smooth muscle actin were significantly increased in the neointima compared to growing vessels. U-PA was moderately increased in growing vessels. TIMP-2 was not detectable in collaterals. We conclude that expression of MMP-2 and 9, TIMP-1 and PAI-1 showed a spatial and temporal pattern which is closely associated with the development of collateral vessels. The shift of the balance between proteolysis and antiproteolysis is regulated not only by MMPs and TIMP-1, but also by the PA-PAI system.