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1.
J Math Biol ; 72(3): 649-81, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26001742

RESUMO

The paper is devoted to mathematical modelling of clot growth in blood flow. Great complexity of the hemostatic system dictates the need of usage of the mathematical models to understand its functioning in the normal and especially in pathological situations. In this work we investigate the interaction of blood flow, platelet aggregation and plasma coagulation. We develop a hybrid DPD-PDE model where dissipative particle dynamics (DPD) is used to model plasma flow and platelets, while the regulatory network of plasma coagulation is described by a system of partial differential equations. Modelling results confirm the potency of the scenario of clot growth where at the first stage of clot formation platelets form an aggregate due to weak inter-platelet connections and then due to their activation. This enables the formation of the fibrin net in the centre of the platelet aggregate where the flow velocity is significantly reduced. The fibrin net reinforces the clot and allows its further growth. When the clot becomes sufficiently large, it stops growing due to the narrowed vessel and the increase of flow shear rate at the surface of the clot. Its outer part is detached by the flow revealing the inner part covered by fibrin. This fibrin cap does not allow new platelets to attach at the high shear rate, and the clot stops growing. Dependence of the final clot size on wall shear rate and on other parameters is studied.


Assuntos
Coagulação Sanguínea/fisiologia , Plaquetas/fisiologia , Fibrina/fisiologia , Modelos Biológicos , Animais , Biologia Computacional , Hemorreologia , Hemostasia/fisiologia , Humanos , Conceitos Matemáticos , Adesividade Plaquetária/fisiologia , Agregação Plaquetária/fisiologia
2.
Acta Biotheor ; 63(3): 283-94, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25822060

RESUMO

This paper is devoted to computer modelling of the development and regeneration of multicellular biological structures. Some species (e.g. planaria and salamanders) are able to regenerate parts of their body after amputation damage, but the global rules governing cooperative cell behaviour during morphogenesis are not known. Here, we consider a simplified model organism, which consists of tissues formed around special cells that can be interpreted as stem cells. We assume that stem cells communicate with each other by a set of signals, and that the values of these signals depend on the distance between cells. Thus the signal distribution characterizes location of stem cells. If the signal distribution is changed, then the difference between the initial and the current signal distribution affects the behaviour of stem cells-e.g. as a result of an amputation of a part of tissue the signal distribution changes which stimulates stem cells to migrate to new locations, appropriate for regeneration of the proper pattern. Moreover, as stem cells divide and form tissues around them, they control the form and the size of regenerating tissues. This two-level organization of the model organism, with global regulation of stem cells and local regulation of tissues, allows its reproducible development and regeneration.


Assuntos
Morfogênese/fisiologia , Regeneração/fisiologia , Animais , Padronização Corporal , Diferenciação Celular , Movimento Celular , Simulação por Computador , Modelos Biológicos , Modelos Estatísticos , Transdução de Sinais , Células-Tronco/citologia
3.
J Theor Biol ; 337: 30-41, 2013 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-23916879

RESUMO

Hemostatic plug covering the injury site (or a thrombus in the pathological case) is formed due to the complex interaction of aggregating platelets with biochemical reactions in plasma that participate in blood coagulation. The mechanisms that control clot growth and which lead to growth arrest are not yet completely understood. We model them with numerical simulations based on a hybrid DPD-PDE model. Dissipative particle dynamics (DPD) is used to model plasma flow with platelets while fibrin concentration is described by a simplified reaction-diffusion-advection equation. The model takes into account consecutive stages of clot growth. First, a platelet is weakly connected to the clot and after some time this connection becomes stronger due to other surface receptors involved in platelet adhesion. At the same time, the fibrin mesh is formed inside the clot. This becomes possible because flow does not penetrate the clot and cannot wash out the reactants participating in blood coagulation. Platelets covered by the fibrin mesh cannot attach new platelets. Modelling shows that the growth of a hemostatic plug can stop as a result of its exterior part being removed by the flow thus exposing its non-adhesive core to the flow.


Assuntos
Hemorreologia , Modelos Biológicos , Trombose/patologia , Coagulação Sanguínea , Plaquetas/metabolismo , Simulação por Computador , Fibrina/metabolismo , Humanos , Trombose/metabolismo
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