Mechanisms of platelet capture at very high shear

Arterial thrombus forms from the capture and accumulation of circulating platelets on a stenosis. As the thrombus grows, the lumen becomes further stenotic producing very high shear rates as the blood velocities increase through the narrowed cross-section. This study explores the molecular binding c...

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Bibliographic Details
Main Author: Wellings, Peter John
Published: Georgia Institute of Technology 2011
Subjects:
VWF
Online Access:http://hdl.handle.net/1853/39582
id ndltd-GATECH-oai-smartech.gatech.edu-1853-39582
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spelling ndltd-GATECH-oai-smartech.gatech.edu-1853-395822013-01-07T20:37:38ZMechanisms of platelet capture at very high shearWellings, Peter JohnActivationThrombosisElongationReceptor densityVWFPlatelet adhesionArteries StenosisShear (Mechanics)Blood platelets AggregationArterial thrombus forms from the capture and accumulation of circulating platelets on a stenosis. As the thrombus grows, the lumen becomes further stenotic producing very high shear rates as the blood velocities increase through the narrowed cross-section. This study explores the molecular binding conditions that may occur under these pathologic shear conditions where circulating platelets must adhere quickly and with strong bonds. Platelets binding in an arterial stenosis of >75% are subject to drag forces exceeding 10,000 pN. This force can be balanced by 100 simultaneous GPIb-vWFA1 bonds of 100 pN each. The number and density of GPIb on platelets is sufficiently high; however, platelet capture under high shear would require the density of A1 receptors to be increased to over 416 per square micron. A computational model is used to determine platelet capture as a function of shear rate, surface receptor density, surface contact and kinetic binding rate. A1 density could be increased by a combination of vWF events of: i) plasma vWF attach to the thrombus surface and elongate under shear; ii) the elongated vWF strands create a net with 3-D pockets; and iii) additional vWF is released from mural platelets by activation under shear. With all three events, A1 density matches the existing high GPIbα densities to provide sufficient multivalency for capture at 100,000 s-1 with greater than 170 bonds per platelet. If the on-rate is greater than 108 M-1s-1, then a platelet could be captured within 15 microseconds, the amount of time available to form bonds before the platelet is swept away. This mechanism of platelet capture allows for the rapid platelet accumulation in atherothombosis seen clinically and in high shear experiments.Georgia Institute of Technology2011-07-06T16:48:52Z2011-07-06T16:48:52Z2011-04-05Thesishttp://hdl.handle.net/1853/39582
collection NDLTD
sources NDLTD
topic Activation
Thrombosis
Elongation
Receptor density
VWF
Platelet adhesion
Arteries Stenosis
Shear (Mechanics)
Blood platelets Aggregation
spellingShingle Activation
Thrombosis
Elongation
Receptor density
VWF
Platelet adhesion
Arteries Stenosis
Shear (Mechanics)
Blood platelets Aggregation
Wellings, Peter John
Mechanisms of platelet capture at very high shear
description Arterial thrombus forms from the capture and accumulation of circulating platelets on a stenosis. As the thrombus grows, the lumen becomes further stenotic producing very high shear rates as the blood velocities increase through the narrowed cross-section. This study explores the molecular binding conditions that may occur under these pathologic shear conditions where circulating platelets must adhere quickly and with strong bonds. Platelets binding in an arterial stenosis of >75% are subject to drag forces exceeding 10,000 pN. This force can be balanced by 100 simultaneous GPIb-vWFA1 bonds of 100 pN each. The number and density of GPIb on platelets is sufficiently high; however, platelet capture under high shear would require the density of A1 receptors to be increased to over 416 per square micron. A computational model is used to determine platelet capture as a function of shear rate, surface receptor density, surface contact and kinetic binding rate. A1 density could be increased by a combination of vWF events of: i) plasma vWF attach to the thrombus surface and elongate under shear; ii) the elongated vWF strands create a net with 3-D pockets; and iii) additional vWF is released from mural platelets by activation under shear. With all three events, A1 density matches the existing high GPIbα densities to provide sufficient multivalency for capture at 100,000 s-1 with greater than 170 bonds per platelet. If the on-rate is greater than 108 M-1s-1, then a platelet could be captured within 15 microseconds, the amount of time available to form bonds before the platelet is swept away. This mechanism of platelet capture allows for the rapid platelet accumulation in atherothombosis seen clinically and in high shear experiments.
author Wellings, Peter John
author_facet Wellings, Peter John
author_sort Wellings, Peter John
title Mechanisms of platelet capture at very high shear
title_short Mechanisms of platelet capture at very high shear
title_full Mechanisms of platelet capture at very high shear
title_fullStr Mechanisms of platelet capture at very high shear
title_full_unstemmed Mechanisms of platelet capture at very high shear
title_sort mechanisms of platelet capture at very high shear
publisher Georgia Institute of Technology
publishDate 2011
url http://hdl.handle.net/1853/39582
work_keys_str_mv AT wellingspeterjohn mechanismsofplateletcaptureatveryhighshear
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