Red cell microparticles produced using high-pressure extrusion enhance both primary and secondary hemostasis
Snigdha Sama1, Sunjoo Cho1, Ashish K Rehni1
1Department of Neurology, Peritz Scheinberg Cerebral Vascular Disease Research Laboratories, University of Miami Miller School of Medicine, 1600 NW 10th Ave RMSB #7046, Miami, FL, 33136, USA.
Pharmacological Reports : PR
|January 8, 2025
Summary
Red blood cell-derived microparticles (RMPs) enhance primary hemostasis by boosting platelet aggregation. RMPs also improve secondary hemostasis by shortening clotting times in specific factor-deficient plasmas.
Area of Science:
- Hematology
- Biomedical Engineering
Background:
- Current excessive bleeding treatments have significant complications.
- Red blood cell-derived microparticles (RMPs) show promise as hemostatic agents with a good safety profile.
- The precise mechanism of RMPs in hemostasis requires further investigation.
Purpose of the Study:
- To elucidate the mechanism of action of RMPs in primary and secondary hemostasis.
- To evaluate the impact of RMPs on platelet aggregation and blood clotting.
- To determine if RMPs influence specific coagulation factor pathways.
Main Methods:
- Platelet aggregometry with inhibitors (eptifibatide, ticagrelor) was used to assess primary hemostasis.
- Thromboelastography with factor-deficient plasmas (VII, VIII, IX, XI, XII) was employed for secondary hemostasis evaluation.
- RMPs were prepared using high-pressure extrusion.
Main Results:
- RMPs significantly enhanced collagen-induced platelet aggregation.
- RMP effects on platelet aggregation were not significant in the presence of platelet inhibitors.
- RMPs significantly reduced clotting times in plasmas deficient in factors VII, VIII, IX, and XI, but not XII.
Conclusions:
- RMPs effectively enhance primary hemostasis.
- RMPs contribute to both pathways of secondary hemostasis.
- RMPs may act via platelet receptors and influence multiple coagulation factors.
Related Concept Videos
Structure and Function of Platelets
974
The cell fragments known as platelets are disc-shaped, with an average diameter of about 3 μm and a thickness of roughly 1 μm. They play a crucial role in the body's vascular clotting system, which also involves plasma proteins, blood cells, and blood vessel tissues.
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...
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...
974
Extrinsic and Intrinsic Pathways of Hemostasis
5.3K
Blood clotting or coagulation involves extrinsic and intrinsic pathways, which ultimately merge into the common pathway, forming a fibrin clot.
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which...
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which...
5.3K
Formation of the Platelet Plug
4.2K
The platelet phase, the second stage of hemostasis, commences around 15-20 seconds after an injury. It follows and overlaps with the vascular phase, during which blood vessels constrict to minimize blood loss.
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...
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...
4.2K
Introduction to Hemostasis
5.4K
Hemostasis is a complex physiological process that prevents excessive bleeding when a blood vessel is injured. It's crucial for maintaining the integrity of the circulatory system, as it ensures that our blood remains fluid while still within the vascular network and yet clots to prevent blood loss upon vessel injury.
The three phases of hemostasis involve many clotting factors present in plasma and several substances released by platelets and injured tissue cells. It is a fast, localized,...
The three phases of hemostasis involve many clotting factors present in plasma and several substances released by platelets and injured tissue cells. It is a fast, localized,...
5.4K
Anticoagulant Drugs: Low-Molecular-Weight Heparins
607
Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
607


