Peristaltic pumps adapted for laminar flow experiments enhance in vitro modeling of vascular cell behavior

被引:18
作者
Abello, Javier [1 ]
Raghavan, Shreya [2 ]
Yien, Yvette Y. [3 ,4 ]
Stratman, Amber N. [1 ]
机构
[1] Washington Univ, Dept Cell Biol & Physiol, Sch Med, St Louis, MO 63130 USA
[2] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
[3] Univ Pittsburgh, Pittsburgh Heart Lung & Blood Vasc Med Inst, Pittsburgh, PA USA
[4] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
ON-A-CHIP; SHEAR-STRESS; ENDOTHELIAL-CELLS; FLUID SHEAR; VE-CADHERIN; EXPRESSION; MIGRATION; DIRECTION; SYSTEM; PHENOTYPES;
D O I
10.1016/j.jbc.2022.102404
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endothelial cells (ECs) are the primary cellular constituent of blood vessels that are in direct contact with hemodynamic forces over their lifetime. Throughout the body, vessels experience different blood flow patterns and rates that alter vascular architecture and cellular behavior. Because of the complexities of studying blood flow in an intact organism, particularly during development, the field has increasingly relied on in vitro modeling of blood flow as a powerful technique for studying hemodynamic-dependent signaling mechanisms in ECs. While commercial flow systems that recirculate fluids exist, many commercially available pumps are peristaltic and best model pulsatile flow conditions. However, there are many important situations in which ECs experience laminar flow conditions in vivo, such as along long straight stretches of the vasculature. To understand EC function under these contexts, it is important to be able to reproducibly model laminar flow conditions in vitro. Here, we outline a method to reliably adapt commercially available peristaltic pumps to study laminar flow conditions. Our proof-of-concept study focuses on 2D models but could be further adapted to 3D environments to better model in vivo scenarios, such as organ development. Our studies make significant inroads into solving technical challenges associated with flow modeling and allow us to conduct functional studies toward understanding the mechanistic role of shear forces on vascular architecture, cellular behavior, and remodeling in diverse physiological contexts.
引用
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页数:11
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