Summary
The proteins of fibrinolysis have been quantified in human thrombi, to assess the
balance between plasminogen activators and their major inhibitor PAI-1. The relative
roles of PAI-1 and α2-AP were also examined since we have previously shown that both platelet PAI-1 and
plasma α2-AP are important determinants of clot lysis in vitro. Extracts and sections were
prepared from human thrombi for quantitative immunoassay and immunohistochemical staining
respectively. PAI-1 and α2-AP were present at high concentrations. Levels of t-PA and t-PA-PAI-1 complex were
relatively low. Staining confirmed the presence of abundant PAI-1, associated primarily
with platelet material within the thrombus and also with fibrin. Staining for α2-AP was also intense and demonstrated strong association with fibrin. The α2-AP concentration was similar to its high plasma concentration, whereas PAI-1 levels
were up to 30 times greater than that in circulating blood, suggesting that active
recruitment of platelets contributes to the high PAI-1 concentration in thrombi.