Abstract

Due to controversial evidence in the literature pertaining to the activity of plasminogen activator inhibitor-1 in platelets, we examined the effects of residual platelets present in plasma (a potential pre-analytical variable) on various plasminogen activator inhibitor-1 and plasminogen activator inhibitor-1-related assays. Blood samples were collected from 151 individuals and centrifuged at 352 and 1500 g to obtain plasma with varying numbers of platelet. In a follow-up study, blood samples were collected from an additional 23 individuals, from whom platelet-poor (2000 g), platelet-containing (352 g) and platelet-rich plasma (200 g) were prepared and analysed as fresh-frozen and after five defrost-refreeze cycles (to determine the contribution of in vitro platelet degradation). Plasminogen activator inhibitor-1 activity, plasminogen activator inhibitor-1 antigen, tissue plasminogen activator/plasminogen activator inhibitor-1 complex, plasma clot lysis time, β-thromboglobulin and plasma platelet count were analysed. Platelet α-granule release (plasma β-thromboglobulin) showed a significant association with plasminogen activator inhibitor-1 antigen levels but weak associations with plasminogen activator inhibitor-1 activity and a functional marker of fibrinolysis, clot lysis time. Upon dividing the study population into quartiles based on β-thromboglobulin levels, plasminogen activator inhibitor-1 antigen increased significantly across the quartiles while plasminogen activator inhibitor-1 activity and clot lysis time tended to increase in the 4th quartile only. In the follow-up study, plasma plasminogen activator inhibitor-1 antigen was also significantly influenced by platelet count in a concentration-dependent manner. Plasma plasminogen activator inhibitor-1 antigen levels increased further after complete platelet degradation. Residual platelets in plasma significantly influence plasma plasminogen activator inhibitor-1 antigen levels mainly through release of latent plasminogen activator inhibitor-1 with limited effects on plasminogen activator inhibitor-1 activity, tissue plasminogen activator/plasminogen activator inhibitor-1 complex or plasma clot lysis time. Platelets may however also have functional effects on plasma fibrinolytic potential in the presence of high platelet counts, such as in platelet-rich plasma.

Highlights

  • Plasminogen activator inhibitor type-1 (PAI-1) is a serine protease inhibitor [1, 2], which acts as a main inhibitor of fibrinolysis [3]

  • When comparing the samples prepared at the two different centrifugation speeds, the 352 g group had significantly higher beta thromboglobulin (βTG) (3263 vs 355 IU/mL; p < 0.0001) and PAI-1 antigen (PAI-1ag) (33.8 vs 20.8 ng/mL; p < 0.0001) levels, compared to the 1500 g group, with borderline significantly higher PAI-1act (2.95 vs 1.91 U/mL; p = 0.03) and longer clot lysis time (CLT) (78.2 vs 74.4 min; p = 0.04)

  • No difference was observed in tissue plasminogen activator (tPA)/PAI-1 complex across the βTG quartiles. βTG was correlated with PAI-1ag (r = 0.66; p

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Summary

Introduction

Plasminogen activator inhibitor type-1 (PAI-1) is a serine protease inhibitor (serpin) [1, 2], which acts as a main inhibitor of fibrinolysis [3]. Elevated plasma PAI-1 levels have been associated with a risk for developing atherothrombosis [4,5,6] due to its antifibrinolytic properties, by reducing the clearance of fibrin in plaques [5], and via its influence on cellular migration, matrix remodelling and activation of growth factors [7, 8]. Plasma PAI-1 exists either in an active or latent form, or in complex with tissue plasminogen activator (tPA) [9,10,11]. The active form of PAI-1 is unstable, with a half-life of approximately two to three hours, after which it will spontaneously convert to the inactive, latent form [9, 12]. PAI-1 is stored in the alpha granules and is released during platelet activation and aggregation [11, 14, 15]

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