Quantifying Shear-induced Margination and Adhesion of Platelets in Microvascular Blood Flow

J Mol Biol. 2023 Jan 15;435(1):167824. doi: 10.1016/j.jmb.2022.167824. Epub 2022 Sep 13.

Abstract

Platelet margination and adhesion are two critical and closely related steps in thrombus formation. Using dissipative particle dynamics (DPD) method that seamlessly models blood cells, blood plasma, and vessel walls with functionalized surfaces, we quantify the shear-induced margination and adhesion of platelets in microvascular blood flow. The results show that the occurrence of shear-induced RBC-platelet collisions has a remarkable influence on the degree of platelet margination. We characterize the lateral motion of individual platelets by a mean square displacement analysis of platelet trajectories, and find that the wall-induced lift force and the shear-induced displacement in wall-bounded flow cause the variation in near-wall platelet distribution. We then investigate the platelet adhesive dynamics under different flow conditions, by conducting DPD simulations of blood flow in a microtube with fibrinogen-coated wall surfaces. We find that the platelet adhesion is enhanced with the increase of fibrinogen concentration level but decreased with the increase of shear rate. These results are consistent with available experimental results. In addition, we demonstrate that the adherent platelets have a negative impact on the margination dynamics of the circulating platelets, which is mainly due to the climbing effect induced by the adherent ones. Taken together, these findings provide useful insights into the platelet margination and adhesion dynamics, which may facilitate the understanding of the predominant processes governing the initial stage of thrombus formation.

Keywords: dissipative particle dynamics; microvascular blood flow; platelet adhesion; platelet margination; protein-membrane interaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Platelets*
  • Fibrinogen / metabolism
  • Humans
  • Microcirculation
  • Microvessels* / physiopathology
  • Platelet Adhesiveness*
  • Thrombosis* / physiopathology

Substances

  • Fibrinogen