Evidence map›Paper›PMID 39212493›Full record

ArticleBioscience reports2024

Integration of clotting and fibrinolysis: central role of platelets and factor XIIIa.

Irina Patalakh, Olga Revka, Agata Gołaszewska, Natalia Bielicka, Tomasz Misztal

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Article in Bioscience reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Irina PatalakhDepartment of Chemistry and Biochemistry of Enzymes, Palladin Institute of Biochemistry of the National Academy of Sciences of Ukraine, Ukraine.
Olga RevkaDepartment of Chemistry and Biochemistry of Enzymes, Palladin Institute of Biochemistry of the National Academy of Sciences of Ukraine, Ukraine.
Agata GołaszewskaDepartment of General and Experimental Pathology, Medical University of Białystok, 15089 Białystok, Poland.
Natalia BielickaDepartment of Biopharmacy and Radiopharmacy, Medical University of Bialystok, Poland.
Tomasz MisztalDepartment of Physical Chemistry, Medical University of Bialystok, Poland.ORCID 0000-0002-5403-9467

Funding

Uniwersytet Medyczny w Bialymstoku (Medical University of Bialystok) SUB/2/DN/20/001/2201
6 · The paper itself

Abstract

purposeThe aim of the present study was to establish the role of platelets and activated factor XIIIa (FXIIIa) in the structuring of the fibrin network as well as to clarify the effect of network compaction on clot lysis.

methodsTurbidimetry was used for the one-stage clotting test where platelet-free plasma (PFP) is regarded as single factor-deficient plasma (platelets as lacking factor) and autologous platelet-rich plasma (PRP) as deficiency corrected plasma. Structural features of the developed and subsequently lysed fibrin network, formed under static and flow conditions, were visualized by confocal microscopy.

resultsThrombin-initiated plasma clotting revealed changes in the shape of the absorption curve, more pronounced in the presence of platelets. These changes correlate with the transformation of the fibrin scaffold during clot maturing. With the combined action of platelets, thrombin and Ca2+, plasma clotting passes through two phases: initial formation of a platelet-fibrin network (first peak in the polymerization curve), and then the compaction of fibrin, driven by FXIIIa (the second peak) which can be further modulate by the contractile action of platelets. These structural changes, mediated by platelets and FXIIIa, have been shown to determine subsequent clot lysis.

conclusionsPlatelet aggregates serve as organizing centers that determine the distribution of fibrin in clot volume. The openwork structure of the platelet-transformed fibrin provides the necessary prerequisites for its timely lysis. The revealed aspects of the interaction of platelets and FXIIIa, which accompanies the maturation of a fibrin clot, may lead to new approaches in the pharmacological correction of disorders associated with both thrombotic episodes and bleeding tendency.

Indexed as

Blood CoagulationBlood PlateletsFactor XIIIaFibrinFibrinolysisThrombinHumansPlatelet AggregationPlatelet-Rich PlasmaFactor XIIIaFibrinThrombinclottingfactor XIIIafibrin networkinternal fibrinolysisplatelet rich plasma

Identifiers

PMID39212493
PMCPMC11427729

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