Exploiting the superior protein resistance of polymer brushes to control single cell adhesion and polarisation at the micron scale

被引:98
作者
Gautrot, Julien E. [1 ]
Trappmann, Britta [1 ]
Oceguera-Yanez, Fabian [2 ]
Connelly, John [2 ]
He, Ximin [1 ]
Watt, Fiona M. [2 ]
Huck, Wilhelm T. S. [1 ,3 ]
机构
[1] Univ Cambridge, Melville Lab Polymer Synth, Dept Chem, Cambridge CB2 1EW, England
[2] Univ Cambridge, Wellcome Trust Ctr Stem Cell Res, Cambridge CB2 1RE, England
[3] Radboud Univ Nijmegen, Inst Mol & Mat, NL-6525 AJ Nijmegen, Netherlands
基金
英国惠康基金;
关键词
Polymer brush; Extra-cellular matrix; Patterning; Single cell; Cell polarisation; TRANSFER RADICAL POLYMERIZATION; SURFACE-INITIATED POLYMERIZATIONS; HUMAN EPIDERMAL-KERATINOCYTES; EXTRACELLULAR-MATRIX; STEM-CELLS; POLARITY; GROWTH; SHAPE; DIFFERENTIATION; MICROARRAYS;
D O I
10.1016/j.biomaterials.2010.02.066
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The control of the cell microenvironment on model patterned substrates allows the systematic study of cell biology in well defined conditions, potentially using automated systems. The extreme protein resistance of poly(oligo(ethylene glycol methacrylate)) (POEGMA) brushes is exploited to achieve high fidelity patterning of single cells. These coatings can be patterned by soft lithography on large areas (a microscope slide) and scale (substrates were typically prepared in batches of 200). The present protocol relies on the adsorption of extra-cellular matrix (ECM) proteins on unprotected areas using simple incubation and washing steps. The stability of POEGMA brushes, as examined via ellipsometry and SPR, is found to be excellent, both during storage and cell culture. The impact of substrate treatment, brush thickness and incubation protocol on ECM deposition, both for ultra-thin gold and glass substrates, is investigated via fluorescence microscopy and AFM. Optimised conditions result in high quality ECM patterns at the micron scale, even on glass substrates, that are suitable for controlling cell spreading and polarisation. These patterns are compatible with state-of-the-art technologies (fluorescence microscopy, FRET) used for live cell imaging. This technology, combined with single cell analysis methods, provides a platform for exploring the mechanisms that regulate cell behaviour. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5030 / 5041
页数:12
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