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

被引:3
作者
Yuan, Wei-Mo [1 ]
Xue, Chun-Dong [2 ]
Qin, Kai-Rong [2 ]
机构
[1] Dalian Univ Technol, Fac Elect Informat & Elect Engn, Sch Biomed Engn, 2,Linggong Rd, Dalian 116024, Liaoning, Peoples R China
[2] Dalian Univ Technol, Sch Optoelect Engn & Instrumentat Sci, 2 Linggong Rd, Dalian 116024, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Vascular endothelial cells; Intracellular calcium response; Microfluidic experiment; Single cell dynamics; Mechanobiology model; Cellular surface tension; INDUCED ATP RELEASE; FLUID SHEAR-STRESS; MEMBRANE TENSION; MATHEMATICAL-MODEL; MEDIATED CALCIUM; CA2+ INFLUX; FLOW; DEFORMATION; CONTRACTION; EXOCYTOSIS;
D O I
10.1007/s10237-020-01368-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:55 / 67
页数:13
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