Related Experiment Video
Updated: Mar 29, 2026

Author Spotlight: Deciphering Coagulation Disorders in Traumatic Brain Injury Patients
Published on: August 4, 2023
Impact of microparticles derived from erythrocytes on fibrinolysis
Grigory Levin1, Ekaterina Sukhareva2, Athina Lavrentieva3
1Federal State Budgetary Institution "Privolzhsky Federal Research Medical Centre" of the Ministry of Health of the Russian Federation, 18, Verhne-Volzhskaya Naberezhnaya, Nizhny Novgorod, Russia, 603155. levin@unn.ac.ru.
Abstract:
It has long been known that negatively charged membranes of erythrocyte-derived microparticles display procoagulant activity. However, relatively little is known about the possible fibrinolytic activity of such microparticles. This issue becomes particularly important during red blood cell storage, which significantly increases the number of microparticles. Whole blood was collected from 30 healthy donors. Microparticles were isolated on days 7, 14, 21, and 28 of erythrocyte storage. The effect of microparticles on the fibrinolytic activity of the donor plasma was determined by coagulation and optical (chromogenic substrate) methods. We demonstrated that erythrocyte microparticles had a prominent fibrinolytic activity which cleaves not only fibrin but also chromogenic substrates. Microparticles present fibrinolytic activity mainly due to the presence of plasminogen on them. Microparticles derived from erythrocytes significantly enhance cleavage of the chromogenic substrate by the streptokinase-plasminogen complex, but to a lesser extent accelerate euglobulin clot lysis time. Erythrocyte-derived microparticles display prominent fibrinolytic activity, which significantly decreases during storage of red blood cells.
Insights
Erythrocyte microparticles exhibit significant fibrinolytic activity, primarily due to plasminogen. This activity diminishes as red blood cells are stored, impacting blood product safety.
Area of Science:
- Hematology
- Biochemistry
- Thrombosis and Hemostasis
Background:
- Erythrocyte-derived microparticles (EMPs) are known for procoagulant activity.
- Fibrinolytic activity of EMPs is less understood, especially during red blood cell storage.
- Increased EMPs during storage raise concerns about their hemostatic balance.
Purpose of the Study:
- To investigate the fibrinolytic activity of EMPs.
- To determine the impact of red blood cell storage duration on EMP fibrinolytic potential.
- To elucidate the mechanisms underlying EMP-associated fibrinolysis.
Main Methods:
- Isolation of EMPs from stored erythrocytes at various time points (7, 14, 21, 28 days).
- Assessment of EMPs' effect on plasma fibrinolytic activity using coagulation assays.
- Evaluation of EMPs' interaction with chromogenic substrates and plasminogen.
Main Results:
- EMPs demonstrate significant fibrinolytic activity, cleaving fibrin and chromogenic substrates.
- Plasminogen adsorbed onto EMPs is the primary driver of their fibrinolytic capacity.
- EMPs enhance streptokinase-plasminogen complex activity but have a lesser effect on euglobulin clot lysis time.
- Fibrinolytic activity of EMPs decreases notably with prolonged erythrocyte storage.
Conclusions:
- Erythrocyte-derived microparticles possess inherent and significant fibrinolytic properties.
- The fibrinolytic potential of EMPs is largely attributed to bound plasminogen.
- Storage of red blood cells leads to a decline in the fibrinolytic activity of EMPs.
Related Concept Videos
Clot Retraction and Fibrinolysis
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Structure and Function of Platelets
Platelets are continually replenished, circulating in the bloodstream for 9-12 days before being removed by phagocytes, primarily in the spleen. A microliter of circulating blood contains between 150,000 and 450,000...
Formation of the Platelet Plug
As the injured blood vessel contracts, endothelial cells undergo contraction, revealing collagen fibers in the basement membrane and underlying connective tissue. Furthermore, the plasma membrane of endothelial cells becomes adhesive, preparing the site for platelet adhesion. Platelets...

