Chopard Bastien, de Sousa Daniel Ribeiro, Lätt Jonas, Mountrakis Lampros, Dubois Frank, Yourassowsky Catherine, Van Antwerpen Pierre, Eker Omer, Vanhamme Luc, Perez-Morga David, Courbebaisse Guy, Lorenz Eric, Hoekstra Alfons G, Boudjeltia Karim Zouaoui
Comupter Science Department, University of Geneva, CUI, 7 route de Drize, 1227 Carouge, Switzerland.
Laboratory of Experimental Medicine (ULB 222 Unit), Université Libre de Bruxelles (ULB), CHU de Charleroi, Belgium.
R Soc Open Sci. 2017 Apr 12;4(4):170219. doi: 10.1098/rsos.170219. eCollection 2017 Apr.
The early stages of clot formation in blood vessels involve platelet adhesion-aggregation. Although these mechanisms have been extensively studied, gaps in their understanding still persist. We have performed detailed experiments, using the well-known Impact-R device, and developed a numerical model to better describe and understand this phenomenon. Unlike previous studies, we took into account the differential role of pre-activated and non-activated platelets, as well as the three-dimensional nature of the aggregation process. Our investigation reveals that blood albumin is a major parameter limiting platelet aggregate formation in our experiment. Simulations are in very good agreement with observations and provide quantitative estimates of the adhesion and aggregation rates that are hard to measure experimentally. They also provide a value of the effective diffusion of platelets in blood subject to the shear rate produced by the Impact-R.
血管中血栓形成的早期阶段涉及血小板黏附-聚集。尽管这些机制已得到广泛研究,但在对其理解上仍存在差距。我们使用著名的Impact-R装置进行了详细实验,并开发了一个数值模型,以更好地描述和理解这一现象。与先前的研究不同,我们考虑了预激活和未激活血小板的不同作用,以及聚集过程的三维性质。我们的研究表明,血液白蛋白是限制我们实验中血小板聚集体形成的主要参数。模拟结果与观察结果非常吻合,并提供了难以通过实验测量的黏附率和聚集率的定量估计。它们还给出了在Impact-R产生的剪切率作用下血小板在血液中有效扩散的值。