A shear gradient-dependent platelet aggregation mechanism drives thrombus formation

被引:672
作者
Nesbitt, Warwick S. [1 ]
Westein, Erik [1 ]
Tovar-Lopez, Francisco Javier [2 ]
Tolouei, Elham [3 ]
Mitchell, Arnan [2 ]
Fu, Jia [1 ]
Carberry, Josie [3 ]
Fouras, Andreas [4 ]
Jackson, Shaun P. [1 ]
机构
[1] Monash Univ, Australian Ctr Blood Dis, Melbourne, Vic 3004, Australia
[2] RMIT Univ, Sch Elect & Comp Engn, Microelect & Mat Technol Ctr, Melbourne, Vic, Australia
[3] Monash Univ, Dept Mech Engn, Clayton, Vic 3168, Australia
[4] Monash Univ, Div Biol Engn, Clayton, Vic, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
ADHESIVE INTERACTIONS; IN-VIVO; ACTIVATION; MODEL; FLOW; IDENTIFICATION; TRANSLOCATION;
D O I
10.1038/nm.1955
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Platelet aggregation at sites of vascular injury is essential for hemostasis and arterial thrombosis. It has long been assumed that platelet aggregation and thrombus growth are initiated by soluble agonists generated at sites of vascular injury. By using high-resolution intravital imaging techniques and hydrodynamic analyses, we show that platelet aggregation is primarily driven by changes in blood flow parameters (rheology), with soluble agonists having a secondary role, stabilizing formed aggregates. We find that in response to vascular injury, thrombi initially develop through the progressive stabilization of discoid platelet aggregates. Analysis of blood flow dynamics revealed that discoid platelets preferentially adhere in low-shear zones at the downstream face of forming thrombi, with stabilization of aggregates dependent on the dynamic restructuring of membrane tethers. These findings provide insight into the prothrombotic effects of disturbed blood flow parameters and suggest a fundamental reinterpretation of the mechanisms driving platelet aggregation and thrombus growth.
引用
收藏
页码:665 / U146
页数:11
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