Articles |
From the Department of Medicine and Therapeutics (L.A.R., B.B.), the Department of Molecular and Cell Biology (L.A.R., N.A.B.), and the Department of Pathology (P.A.J.B.), University of Aberdeen, Scotland, UK.
Correspondence to Dr L. A. Robbie, Department of Medicine and Therapeutics, University of Aberdeen, Foresterhill, Aberdeen AB9 2ZD, Scotland, UK. E-mail larobbie@abdn.ac.uk.
Abstract The proteins of the fibrinolytic system have been
examined in the human normal and atherosclerotic arterial
wall by immunohistochemical techniques and by quantitative immunoassay
of extracts. The concentration of plasminogen
activator inhibitor-1 (PAI-1) increased
significantly during the progression from normal vessels to fatty
streaks to the developed atherosclerotic plaque. Staining for PAI-1 was
strongly positive, particularly in the areas adjacent to the plaque. In
these areas, PAI-1 appeared to be colocalized with its binding protein
vitronectin.
2-Antiplasmin
(
2-AP) was present in the aorta at even higher
concentrations than PAI-1; a small but significant increase was seen in
some atherosclerotic compared with normal vessel walls. Tissue
plasminogen activator (TPA) showed the opposite
trend, being lowest in lesions with plaque. Thus, higher concentrations
of the two principal inhibitors of
fibrinolysis, PAI-1 and
2-AP, together
with lower levels of TPA, are characteristic of advanced
atheromatous lesions. Alteration in the balance of the
fibrinolytic system, favoring its inhibition, may predispose to the
development or maintenance of atherosclerotic plaque.
Key Words: atherosclerosis fibrinolysis PAI-1
2-AP
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