Guilbert Cyrille, Chayer Boris, Allard Louise, Yu François T H, Cloutier Guy
Laboratory of Biorheology and Medical Ultrasonics, University of Montreal Hospital Research Center (CRCHUM), Montréal, Québec, Canada.
Laboratory of Biorheology and Medical Ultrasonics, University of Montreal Hospital Research Center (CRCHUM), Montréal, Québec, Canada; Institute of Biomedical Engineering, University of Montreal, Montréal, Québec, Canada; Department of Radiology, Radio-oncology and Nuclear Medicine, University of Montreal, Montréal, Québec, Canada.
J Biomech. 2017 Aug 16;61:26-33. doi: 10.1016/j.jbiomech.2017.06.044. Epub 2017 Jul 5.
Blood platelets when activated are involved in the mechanisms of hemostasis and thrombosis, and their migration toward injured vascular endothelium necessitates interaction with red blood cells (RBCs). Rheology co-factors such as a high hematocrit and a high shear rate are known to promote platelet mass transport toward the vessel wall. Hemodynamic conditions promoting RBC aggregation may also favor platelet migration, particularly in the venous system at low shear rates. The aim of this study was to confirm experimentally the impact of RBC aggregation on platelet-sized micro particle migration in a Couette flow apparatus. Biotin coated micro particles were mixed with saline or blood with different aggregation tendencies, at two shear rates of 2 and 10s and three hematocrits ranging from 20 to 60%. Streptavidin membranes were respectively positioned on the Couette static and rotating cylinders upon which the number of adhered fluorescent particles was quantified. The platelet-sized particle adhesion on both walls was progressively enhanced by increasing the hematocrit (p<0.001), reducing the shear rate (p<0.001), and rising the aggregation of RBCs (p<0.001). Particle count was minimum on the stationary cylinder when suspended in saline at 2s (57±33), and maximum on the rotating cylinder at 60% hematocrit, 2s and the maximum dextran-induced RBC aggregation (2840±152). This fundamental study is confirming recent hypotheses on the role of RBC aggregation on venous thrombosis, and may guide molecular imaging protocols requiring injecting active labeled micro particles in the venous flow system to probe human diseases.
血小板激活后参与止血和血栓形成机制,其向受损血管内皮的迁移需要与红细胞(RBC)相互作用。已知诸如高血细胞比容和高剪切速率等流变学辅助因素可促进血小板向血管壁的质量传输。促进RBC聚集的血流动力学条件也可能有利于血小板迁移,特别是在低剪切速率的静脉系统中。本研究的目的是通过实验证实RBC聚集对库埃特流动装置中血小板大小的微粒迁移的影响。将生物素包被的微粒与具有不同聚集倾向的盐水或血液混合,在2和10秒的两个剪切速率以及20%至60%的三个血细胞比容下进行。链霉亲和素膜分别放置在库埃特静态和旋转圆柱体上,对其上粘附的荧光微粒数量进行定量。通过增加血细胞比容(p<0.001)、降低剪切速率(p<0.001)和增加RBC聚集(p<0.001),两壁上血小板大小的微粒粘附逐渐增强。当在2秒时悬浮在盐水中时,固定圆柱体上的微粒计数最少(57±33),而在60%血细胞比容、2秒和最大右旋糖酐诱导的RBC聚集(2840±152)时,旋转圆柱体上的微粒计数最多。这项基础研究证实了最近关于RBC聚集在静脉血栓形成中作用的假说,并可能指导在静脉血流系统中注射活性标记微粒以探测人类疾病的分子成像方案。