Regulating Cell-Material Interfacial Interactions through Selective Cellular Resistance

被引:0
|
作者
Hao, Hongye [1 ,2 ,3 ]
Chen, Yifeng [2 ]
Yu, Weijiang [2 ]
Wang, Xingwang [2 ]
Wang, Cong [2 ]
Zhang, Peng [1 ,2 ,3 ]
Ji, Jian [1 ,2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Sch Med, State Key Lab Transvasc Implantat Devices, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, Dept Polymer Sci & Engn, MOE, Key Lab Macromol Synth & Functionalizat, Hangzhou 310058, Peoples R China
[3] Zhejiang Univ, Int Res Ctr Polymers 10, Int Campus, Haining 314400, Peoples R China
[4] Transvasc Implantat Devices Res Inst China, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
STENT;
D O I
10.1021/jacs.5c01433
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regulating the behavior of different types of cells at the material-tissue interface is pivotal for inducing tissue regeneration. Traditional methods enhance target cell activity using specific ligands such as peptides and antibodies, which have stability issues within biological environments. Herein, we show that selective cell resistance can be realized by fine-tuning the material surface chemistry, achieving strong cell selectivity superior to that of extracellular matrix peptides. A certain degree of adsorption resistance differentially affects the adhesion of various types of cells on material surfaces. Taking this principle into account, a polyethylene glycol (PEG) grafted surface was meticulously fine-tuned to selectively support endothelial cells (ECs) while resisting smooth muscle cell attachment. Mechanistic studies identified that the difference in myosin II expression is crucial for cell selectivity. An EC-selective polymer coating for cardiovascular devices was fabricated to promote rapid surface endothelialization and prevent neointimal hyperplasia in vivo.
引用
收藏
页码:9981 / 9989
页数:9
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