Different expression of MMPs/TIMP-1 in human atherosclerotic lesions.: Relation to plaque features and vascular bed

被引:187
作者
Orbe, J
Fernandez, L
Rodríguez, JA
Rábago, G
Belzunce, M
Monasterio, A
Roncal, C
Páramo, JA
机构
[1] Univ Navarra, Atherosclerosis Res Lab, Sch Med, Div Cardiovasc Pathophysiol, Pamplona 31008, Spain
[2] Univ Navarra Clin, Pamplona, Spain
关键词
metalloproteinases; TIMP-1; atherosclerosis; calcification; collagen; aneurysm;
D O I
10.1016/S0021-9150(03)00251-X
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: Proteolytic imbalance might determine arterial remodeling and plaque destabilization in atherosclerotic vessels. The aim of this study was to examine differences in the patterns of metalloproteinases (MMPs) and MMP inhibitor (TIMP-1) expression in advanced human atheromas, both in relation to the plaque features and the vascular bed involved. Methods and results: Immunohistochemistry for MMP-1, -3, -9 and TIMP- I as well as the collagen content were measured in vascular sections from patients undergoing peripheral revascularization (carotid n = 11, femoral n = 23) and aorto-coronary bypass surgery (mammary arteries n = 20, as controls). Increased expression of all MMPs was detected in atherosclerotic as compared with control sections (P<0.01). Aneurismal plaques showed a significant increase of MMP- I and-3 and a reduction in total collagen (P<0.05) in relation to occlusive lesions. Calcification areas in atherosclerotic plaques were consistently associated with increased TIMP- I expression (P<0.01). Finally, MMP-9 expression was higher in occlusive lesions from carotid than femoral arteries (P<0.01). Conclusions: Aneurysm lesions expressed higher MMP-I and-3 expression than occlusive plaques, and MMP-9 was mainly detected in carotid as compared with femoral arteries. TIMP-1 was associated with arterial calcification. These differences in the MMPs/TIMP- I expression might determine the evolution of advanced atherosclerotic plaques and contribute to its vulnerability. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:269 / 276
页数:8
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