Literature DB >> 21320422

Platelet adhesion from shear blood flow is controlled by near-wall rebounding collisions with erythrocytes.

A A Tokarev1, A A Butylin, F I Ataullakhanov.   

Abstract

The efficacy of platelet adhesion in shear flow is known to be substantially modulated by the physical presence of red blood cells (RBCs). The mechanisms of this regulation remain obscure due to the complicated character of platelet interactions with RBCs and vascular walls. To investigate this problem, we have created a mathematical model that takes into account shear-induced transport of platelets across the flow, platelet expulsion by the RBCs from the near-wall layer of the flow onto the wall, and reversible capture of platelets by the wall and their firm adhesion to it. This model analysis allowed us to obtain, for the first time to our knowledge, an analytical determination of the platelet adhesion rate constant as a function of the wall shear rate, hematocrit, and average sizes of platelets and RBCs. This formula provided a quantitative description of the results of previous in vitro adhesion experiments in perfusion chambers. The results of the simulations suggest that under a wide range of shear rates and hematocrit values, the rate of platelet adhesion from the blood flow is mainly limited by the frequency of their near-wall rebounding collisions with RBCs. This finding reveals the mechanism by which erythrocytes physically control platelet hemostasis.
Copyright © 2011 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21320422      PMCID: PMC3037552          DOI: 10.1016/j.bpj.2010.12.3740

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  51 in total

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Journal:  Thromb Haemost       Date:  1986-06-30       Impact factor: 5.249

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  33 in total

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Review 7.  Tensile and compressive force regulation on cell mechanosensing.

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Review 8.  Platelet "first responders" in wound response, cancer, and metastasis.

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9.  Platelet dynamics in three-dimensional simulation of whole blood.

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10.  Review of quantitative systems pharmacological modeling in thrombosis.

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