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本文引用的文献

1
Shear stress-induced binding of large and unusually large von Willebrand factor to human platelet glycoprotein Ibalpha.剪切应力诱导的大的及异常大的血管性血友病因子与人类血小板糖蛋白Ibalpha的结合。
Ann Biomed Eng. 2004 Jul;32(7):961-9. doi: 10.1023/b:abme.0000032458.88212.54.
2
Signaling through GP Ib-IX-V activates alpha IIb beta 3 independently of other receptors.通过糖蛋白Ib-IX-V的信号传导独立于其他受体激活αIIbβ3。
Blood. 2004 May 1;103(9):3403-11. doi: 10.1182/blood-2003-10-3664. Epub 2004 Jan 15.
3
Kinetics of GPIbalpha-vWF-A1 tether bond under flow: effect of GPIbalpha mutations on the association and dissociation rates.流动状态下糖蛋白Ibα-vWF-A1系链键的动力学:糖蛋白Ibα突变对结合和解离速率的影响
Biophys J. 2003 Dec;85(6):4099-109. doi: 10.1016/S0006-3495(03)74822-X.
4
Alterations in the intrinsic properties of the GPIbalpha-VWF tether bond define the kinetics of the platelet-type von Willebrand disease mutation, Gly233Val.糖基磷脂酰肌醇锚定蛋白α-血管性血友病因子(GPIbalpha-VWF)连接键内在特性的改变决定了血小板型血管性血友病疾病突变Gly233Val的动力学。
Blood. 2003 Jul 1;102(1):152-60. doi: 10.1182/blood-2003-01-0072. Epub 2003 Mar 13.
5
Selectin-like kinetics and biomechanics promote rapid platelet adhesion in flow: the GPIb(alpha)-vWF tether bond.类选择素动力学和生物力学促进血小板在血流中快速黏附:糖蛋白Ibα-血管性血友病因子系链键
Biophys J. 2002 Jul;83(1):194-205. doi: 10.1016/S0006-3495(02)75161-8.
6
Comparison of PSGL-1 microbead and neutrophil rolling: microvillus elongation stabilizes P-selectin bond clusters.PSGL-1微珠与中性粒细胞滚动的比较:微绒毛伸长可稳定P-选择素键簇。
Biophys J. 2002 Apr;82(4):1835-47. doi: 10.1016/S0006-3495(02)75534-3.
7
Multiparticle adhesive dynamics: hydrodynamic recruitment of rolling leukocytes.多颗粒黏附动力学:滚动白细胞的流体动力学募集
Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):14919-24. doi: 10.1073/pnas.261272498.
8
Multiparticle adhesive dynamics. Interactions between stably rolling cells.多颗粒黏附动力学。稳定滚动细胞之间的相互作用。
Biophys J. 2001 Aug;81(2):799-813. doi: 10.1016/S0006-3495(01)75742-6.
9
The effect of adsorbed fibrinogen, fibronectin, von Willebrand factor and vitronectin on the procoagulant state of adherent platelets.吸附的纤维蛋白原、纤连蛋白、血管性血友病因子和玻连蛋白对黏附血小板促凝状态的影响。
Biomaterials. 2000 Nov;21(22):2243-52. doi: 10.1016/s0142-9612(00)00150-2.
10
Mapping the glycoprotein Ib-binding site in the von willebrand factor A1 domain.定位血管性血友病因子A1结构域中糖蛋白Ib结合位点。
J Biol Chem. 2000 Jun 23;275(25):19098-105. doi: 10.1074/jbc.M002292200.

流动状态下血小板与血管性血友病因子瞬时黏附的力学原理。

Mechanics of transient platelet adhesion to von Willebrand factor under flow.

作者信息

Mody Nipa A, Lomakin Oleg, Doggett Teresa A, Diacovo Thomas G, King Michael R

机构信息

Department of Biomedical Engineering, University of Rochester, NY 14642, USA.

出版信息

Biophys J. 2005 Feb;88(2):1432-43. doi: 10.1529/biophysj.104.047001. Epub 2004 Nov 8.

DOI:10.1529/biophysj.104.047001
PMID:15533923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1305145/
Abstract

A primary and critical step in platelet attachment to injured vascular endothelium is the formation of reversible tether bonds between the platelet glycoprotein receptor Ibalpha and the A1 domain of surface-bound von Willebrand factor (vWF). Due to the platelet's unique ellipsoidal shape, the force mechanics involved in its tether bond formation differs significantly from that of leukocytes and other spherical cells. We have investigated the mechanics of platelet tethering to surface-immobilized vWF-A1 under hydrodynamic shear flow. A computer algorithm was used to analyze digitized images recorded during flow-chamber experiments and track the microscale motions of platelets before, during, and after contact with the surface. An analytical two-dimensional model was developed to calculate the motion of a tethered platelet on a reactive surface in linear shear flow. Through comparison of the theoretical solution with experimental observations, we show that attachment of platelets occurs only in orientations that are predicted to result in compression along the length of the platelet and therefore on the bond being formed. These results suggest that hydrodynamic compressive forces may play an important role in initiating tether bond formation.

摘要

血小板附着于受损血管内皮的一个主要且关键的步骤是血小板糖蛋白受体Ibalpha与表面结合的血管性血友病因子(vWF)的A1结构域之间形成可逆的系链键。由于血小板独特的椭圆形形状,其系链键形成过程中涉及的力的力学原理与白细胞和其他球形细胞有显著差异。我们研究了在流体动力剪切流作用下血小板与表面固定的vWF-A1系链的力学原理。使用计算机算法分析流动腔实验中记录的数字化图像,并跟踪血小板在接触表面之前、期间和之后的微观运动。建立了一个二维分析模型来计算线性剪切流中反应表面上系链血小板的运动。通过将理论解与实验观察结果进行比较,我们表明血小板仅在预计会导致沿血小板长度方向压缩从而形成键的取向下发生附着。这些结果表明流体动力压缩力可能在启动系链键形成中起重要作用。