The intracellular calcium dynamics in a single vascular endothelial cell being squeezed through a narrow microfluidic channel

Revealing the mechanisms underlying the intracellular calcium responses in vascular endothelial cells (VECs) induced by mechanical stimuli contributes to a better understanding for vascular diseases, including hypertension, atherosclerosis, and aneurysm. Combining with experimental measurement and Computational Fluid Dynamics simulation, we developed a mechanobiological model to investigate the intracellular [Ca2+] response in a single VEC being squeezed through narrow microfluidic channel. The time-dependent cellular surface tension dynamics was quantified throughout the squeezing process. In our model, the various Ca(2+)signaling pathways activated by mechanical stimulation is fully considered. The simulation results of our model exhibited well agreement with our experimental results. By using the model, we theoretically explored the mechanism of the two-peak intracellular [Ca2+] response in single VEC being squeezed through narrow channel and made some testable predictions for guiding experiment in the future.

Automated summary

Studying the mechanisms of intracellular calcium responses in vascular endothelial cells induced by mechanical stimuli provides insights into vascular diseases. A mechanobiological model was developed to investigate the intracellular [Ca2+] response in single VECs being squeezed through narrow microfluidic channels, with simulation results aligning closely with experimental findings. The model was used to explore the mechanism of the two-peak intracellular [Ca2+] response in single VECs and make testable predictions for future experiments.