Effect of flow on ATP/ADP concentration at the endothelial cell surface: interplay between shear stress and mass transport

TL;DR

This study develops a mathematical model to analyze how shear stress and mass transport influence ATP/ADP concentrations on endothelial cell surfaces under flow, revealing complex interactions affected by cell density.

Contribution

The paper introduces a new computational model that quantifies the relative effects of shear stress and transport on nucleotide regulation at endothelial surfaces, considering cell density effects.

Findings

Transport significantly influences nucleotide concentration at certain shear stresses.

Cell density amplifies the effect of transport on ATP/ADP levels.

Transport and shear stress interact complexly to regulate surface nucleotide concentrations.

Abstract

The nucleotides ATP and ADP regulate many aspects of endothelial cell (EC) biology, including intracellular calcium concentrations, focal adhesion activation, cytoskeletal organization, and cellular motility. In vivo, ECs are constantly under flow, and the concentration of ATP/ADP on the EC surface is determined by the combined effects of nucleotide convective and diffusive transport as well as hydrolysis by ectonucleotidases on the EC surface. In addition, experiments have demonstrated that flow induces ATP release from the cells. Previously computational models have incorporated the above effects and thus described concentration at the EC surface. However, it remains unclear what physical processes are responsible for nucleotide regulation. While some EC responses to flow have been shown to be directly driven by shear stress, others appear to also involve a non-negligible contribution of transport. In the present work, we develop a mathematical model and perform numerical simulations to investigate the relative contributions of shear stress and transport to nucleotide concentration at the EC surface, with the effect of cell density. Because in vitro experiments are performed by using confluent cells in some cases and subconfluent cells in other cases, we also investigate the effect of cell density on the results. The outcomes of the simulations demonstrate a complex interplay between shear stress and transport such that transport has a significant contribution at certain shear stress values but not at others. The effect of transport on nucleotide concentration increases with cell density. The present findings enhance our understanding of the mechanisms that govern the regulation of such molecules at the EC surface under flow. The implications of these findings for downstream responses such as cellular motility merit future investigation.