Directing cell migration using micropatterned and dynamically adhesive polymer brushes

被引:44
|
作者
Costa, Patricia [1 ]
Gautrot, Julien E. [2 ]
Connelly, John T. [1 ,3 ]
机构
[1] Univ London, Barts & London Sch Med & Dent, London E1 2AT, England
[2] Univ London, Sch Engn & Mat Sci, London E1 4NS, England
[3] Univ London, Inst Bioengn, London E1 2AT, England
基金
英国生物技术与生命科学研究理事会;
关键词
Polymer brush; Micropattern; Click chemistry; Cell migration; Integrin; CLICK CHEMISTRY; SHAPE; MICROENVIRONMENTS; ORIENTATION; SURFACES; SERUM;
D O I
10.1016/j.actbio.2014.01.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Micropatterning techniques, such as photolithography and microcontact printing, provide robust tools for controlling the adhesive interactions between cells and their extracellular environment. However, the ability to modify these interactions in real time and examine dynamic cellular responses remains a significant challenge. Here we describe a novel strategy to create dynamically adhesive, micropatterned substrates, which afford precise control of cell adhesion and migration over both space and time. Specific functionalization of micropatterned poly(ethylene glycol methacrylate) (POEGMA) brushes with synthetic peptides, containing the integrin-binding arginine-glycine-aspartic acid (RGD) motif, was achieved using thiol-yne coupling reactions. RGD activation of POEGMA brushes promoted fibroblast adhesion, spreading and migration into previously non-adhesive areas, and migration speed could be tuned by adjusting the surface ligand density. We propose that this technique is a robust strategy for creating dynamically adhesive biomaterial surfaces and a useful assay for studying cell migration. (C) 2014 Acts Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2415 / 2422
页数:8
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