Platelet Aggregation and Activation under Complex Patterns of Shear Stress

Arterial stenosis results in a complex pattern of blood flow containing an extremely fast flow in the throat of stenosis and a post-stenosis low flow. The fast flow generates high shear stress that has been demonstrated in vitro to activate and aggregate platelets. One potential problem of these in vitro studies is that platelets are invariably exposed to a high shear stress for a period that is significantly longer than they would have experienced in vivo. More importantly, the role of the post-stenosis low flow in platelet activation and aggregation has not been determined. By exposing platelets to a shear profile that contains both high and low shear segments, we found that platelets aggregate when they are exposed to a high shear stress of 100 dyn/cm(2) for as short as 2.5 s, a period that is significantly shorter than those previously reported (30-120 s). Platelet aggregation under this condition requires a low shear exposure immediately after a high shear pulse, suggesting that post-stenosis low flow enhances platelet aggregation. Furthermore, platelet aggregation under this condition is not activation-dependent because the CD62P expression of sheared platelets is significantly less than that of platelets treated with ADP. Based on these findings, we propose that shear-induced platelet aggregation may be a process of mechanical crosslinking of platelets, requiring minimal platelet activation. This process may function as a protective mechanism to prevent in vivo irreversible platelet activation and aggregation under temporary high shear.

[1]  R. Pélissier,et al.  Experimental analysis of unsteady flows through a stenosis. , 1997, Journal of biomechanics.

[2]  G Cloutier,et al.  Assessment of arterial stenosis in a flow model with power Doppler angiography: accuracy and observations on blood echogenicity. , 2000, Ultrasound in medicine & biology.

[3]  T Shimono,et al.  Mr flow measurement in the internal mammary artery-to-coronary artery bypass graft: comparison with graft stenosis at radiographic angiography. , 2001, Radiology.

[4]  S. Goto,et al.  Enhanced shear-induced platelet aggregation in acute myocardial infarction. , 1999, Circulation.

[5]  M. Deville,et al.  Pulsatile flow of non-Newtonian fluids through arterial stenoses. , 1996, Journal of biomechanics.

[6]  J. Moake,et al.  Platelets and shear stress. , 1996, Blood.

[7]  M Siouffi,et al.  The effect of unsteadiness on the flow through stenoses and bifurcations. , 1984, Journal of biomechanics.

[8]  J. Grotta,et al.  Shear-Induced Platelet Aggregation in Normal Subjects and Stroke Patients , 1995, Thrombosis and Haemostasis.

[9]  D Kilpatrick,et al.  Mathematical modelling of flow through an irregular arterial stenosis. , 1991, Journal of biomechanics.

[10]  D. Ku,et al.  A nonlinear axisymmetric model with fluid-wall interactions for steady viscous flow in stenotic elastic tubes. , 1999, Journal of biomechanical engineering.

[11]  N. Savion,et al.  Transient adhesion refractoriness of circulating platelets under shear stress: the role of partial activation and microaggregate formation by suboptimal ADP concentration , 2001, British journal of haematology.

[12]  M. Deville,et al.  Finite element simulation of pulsatile flow through arterial stenosis. , 1992, Journal of biomechanics.

[13]  T. Nakano,et al.  Increased platelet aggregability in response to shear stress in acute myocardial infarction and its inhibition by combined therapy with aspirin and cilostazol after coronary intervention. , 2000, The American journal of cardiology.

[14]  Brian Savage,et al.  Initiation of Platelet Adhesion by Arrest onto Fibrinogen or Translocation on von Willebrand Factor , 1996, Cell.

[15]  L. McIntire,et al.  Ristocetin-dependent, but not botrocetin-dependent, binding of von Willebrand factor to the platelet glycoprotein Ib-IX-V complex correlates with shear-dependent interactions. , 2001, Blood.

[16]  J. Moake,et al.  Shear-induced platelet aggregation can be mediated by vWF released from platelets, as well as by exogenous large or unusually large vWF multimers, requires adenosine diphosphate, and is resistant to aspirin , 1988 .

[17]  Y. Cho,et al.  Physiological flow simulation in residual human stenoses after coronary angioplasty. , 2000, Journal of biomechanical engineering.

[18]  J D Hellums,et al.  Shear-induced platelet aggregation can be mediated by vWF released from platelets, as well as by exogenous large or unusually large vWF multimers, requires adenosine diphosphate, and is resistant to aspirin. , 1988, Blood.

[19]  J. M. Siegel,et al.  A scaling law for wall shear rate through an arterial stenosis. , 1994, Journal of biomechanical engineering.

[20]  V Deplano,et al.  Experimental and numerical study of pulsatile flows through stenosis: wall shear stress analysis. , 1999, Journal of biomechanics.

[21]  D Saloner,et al.  Influence of stenosis morphology on flow through severely stenotic vessels: implications for plaque rupture. , 2000, Journal of biomechanics.

[22]  S. A. Ahmed,et al.  Pulsatile poststenotic flow studies with laser Doppler anemometry. , 1984, Journal of biomechanics.

[23]  L. McIntire,et al.  Shear-dependent rolling on von Willebrand factor of mammalian cells expressing the platelet glycoprotein Ib-IX-V complex. , 1998, Blood.