Shear stress with appropriate time-step and amplification enhances endothelial cell retention on vascular grafts

被引:15
作者
Liu, Haifeng [1 ]
Gong, Xianghui [1 ]
Jing, Xiaohui [1 ]
Ding, Xili [1 ]
Yao, Yuan [1 ]
Huang, Yan [1 ]
Fan, Yubo [1 ,2 ]
机构
[1] Beihang Univ, Sch Biol Sci & Med Engn, Minist Educ, Key Lab Biomech & Mechanobiol, Beijing, Peoples R China
[2] Natl Res Ctr Rehabil Tech Aids, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
shear stress; time-step; amplification; endothelial cell; silk fibroin vascular graft; FIBRONECTIN MATRIX; IN-VIVO; EXTRACELLULAR-MATRIX; ADHESION; BETA-1-INTEGRIN; EXPRESSION; INTEGRINS; APOPTOSIS; CULTURE; GROWTH;
D O I
10.1002/term.2196
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Endothelial cells (ECs) are sensitive to changes in shear stress. The application of shear stress to ECs has been well documented to improve cell retention when placed into a haemodynamically active environment. However, the relationship between the time-step and amplification of shear stress on EC functions remains elusive. In the present study, human umbilical cord veins endothelial cells (HUVECs) were seeded on silk fibroin nanofibrous scaffolds and were preconditioned by shear stress at different time-steps and amplifications. It is shown that gradually increasing shear stress with appropriate time-steps and amplification could improve EC retention, yielding a complete endothelial-like monolayer both in vitro and in vivo. The mechanism of this improvement is mediated, at least in part, by an upregulation of integrin ss 1 and focal adhesion kinase (FAK) expression, which contributed to fibronectin (FN) assembly enhancement in ECs in response to the shear stress. A modest gradual increase in shear stress was essential to allow additional time for ECs to gradually acclimatize to the changing environment, with the goal of withstanding the physiological levels of shear stress. This study recognized that the time-steps and amplifications of shear stress could regulate EC tolerance to shear stress and the anti-thrombogenicity function of engineered vascular grafts via an extracellular cell matrix-specific, mechanosensitive signalling pathway and might prevent thrombus formation in vivo. Copyright (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:2965 / 2978
页数:14
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