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DOI: 10.1055/a-1957-6817
Plasmin Inhibitor in Health and Diabetes: Role of the Protein as a Therapeutic Target
Abstract
The vascular obstructive thrombus is composed of a mesh of fibrin fibers with blood cells trapped in these networks. Enhanced fibrin clot formation and/or suppression of fibrinolysis are associated with an increased risk of vascular occlusive events. Inhibitors of coagulation factors and activators of plasminogen have been clinically used to limit fibrin network formation and enhance lysis. While these agents are effective at reducing vascular occlusion, they carry a significant risk of bleeding complications. Fibrin clot lysis, essential for normal hemostasis, is controlled by several factors including the incorporation of antifibrinolytic proteins into the clot. Plasmin inhibitor (PI), a key antifibrinolytic protein, is cross-linked into fibrin networks with higher concentrations of PI documented in fibrin clots and plasma from high vascular risk individuals. This review is focused on exploring PI as a target for the prevention and treatment of vascular occlusive disease. We first discuss the relationship between the PI structure and antifibrinolytic activity, followed by describing the function of the protein in normal physiology and its role in pathological vascular thrombosis. Subsequently, we describe in detail the potential use of PI as a therapeutic target, including the array of methods employed for the modulation of protein activity. Effective and safe inhibition of PI may prove to be an alternative and specific way to reduce vascular thrombotic events while keeping bleeding risk to a minimum.
Key Points
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Plasmin inhibitor (PI) is a key protein that inhibits fibrinolysis and stabilizes the fibrin network.
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This review is focused on discussing mechanistic pathways for PI action, role of the molecule in disease states, and potential use as a therapeutic target.
Author Contributions
B.A. and N.K. were responsible for drafting and writing of the manuscript, searching of literature, and interpreting data. M.A. and K.S. were responsible for writing part of the manuscript and provided helpful feedback on specific sections. R.A.A. was responsible for drafting and writing the manuscript and the critical revision of intellectual content. N.P. and S.P. contributed to critically reviewing and editing the manuscript. All authors approved the version for publication.
Publikationsverlauf
Eingereicht: 05. März 2022
Angenommen: 23. September 2022
Accepted Manuscript online:
09. Oktober 2022
Artikel online veröffentlicht:
18. November 2022
© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
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