A multiscale approach for determining the morphology of endothelial cells at a coronary artery

Int J Numer Method Biomed Eng. 2017 Dec;33(12). doi: 10.1002/cnm.2891. Epub 2017 Jun 14.

Abstract

The morphology of endothelial cells (ECs) may be an indication for determining atheroprone sites. Until now, there has been no clinical imaging technique to visualize the morphology of ECs in the arteries. The present study introduces a computational technique for determining the morphology of ECs. This technique is a multiscale simulation consisting of the artery scale and the cell scale. The artery scale is a fluid-structure interaction simulation. The input for the artery scale is the geometry of the coronary artery, that is, the dynamic curvature of the artery due to the cardiac motion, blood flow, blood pressure, heart rate, and the mechanical properties of the blood and the arterial wall, the measurements of which can be obtained for a specific patient. The results of the artery scale are wall shear stress (WSS) and cyclic strains as the mechanical stimuli of ECs. The cell scale is an inventive mass-and-spring model that is able to determine the morphological response of ECs to any combination of mechanical stimuli. The results of the multiscale simulation show the morphology of ECs at different locations of the coronary artery. The results indicate that the atheroprone sites have at least 1 of 3 factors: low time-averaged WSS, high angle of WSS, and high longitudinal strain. The most probable sites for atherosclerosis are located at the bifurcation region and lie on the myocardial side of the artery. The results also indicated that a higher dynamic curvature is a negative factor and a higher pulse pressure is a positive factor for protection against atherosclerosis.

Keywords: atherosclerosis; cell model; fluid-structure interaction; morphology; multiscale simulation.

MeSH terms

  • Cell Shape*
  • Computer Simulation
  • Coronary Vessels / cytology*
  • Coronary Vessels / physiology
  • Cytological Techniques / methods*
  • Endothelial Cells / cytology*
  • Endothelial Cells / physiology
  • Hemodynamics
  • Humans
  • Models, Cardiovascular
  • Shear Strength / physiology
  • Stress, Mechanical