Redox-Triggered Control of Cell Adhesion and Deadhesion on Poly(lysine)-g-poly(ethylene oxide) Adlayers

被引:0
|
作者
Hespel, Louise [1 ]
de Baubigny, Julien Dupre [1 ]
Lalanne, Pierre [1 ]
de Beco, Simon [2 ]
Coppey, Mathieu [2 ]
Villard, Catherine [2 ]
Humblot, Vincent [3 ]
Marie, Emmanuelle [1 ]
Tribet, Christophe [1 ]
机构
[1] Sorbonne Univ, Ecole Normale Super, Dept Chim, CNRS,PASTEUR,PSL Univ, F-75005 Paris, France
[2] Sorbonne Univ, CNRS UMR168, Inst Curie, Lab Phys Chim,PSL Univ, F-75005 Paris, France
[3] Sorbonne Univ, Lab Reactivite Surface, CNRS UMR 7197, 4 Pl Jussieu, F-75005 Paris, France
关键词
redox responsive; dynamic coatings; micropatterns; disulfide; PLL-PEG antifouling; cell adhesion;
D O I
10.1021/acsabm.9b00601
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Spontaneous adsorption of poly(lysine)-g-poly-(ethylene glycol) comb-like copolymers (PLL-g-PEG) is a versatile mean to coat substrates with polymer layers that resist cell adhesion. We prepared redox cleavable PLL-g-PEG to switch adhesion on demand. Redox sensitivity was obtained by introducing disulfide linkers between the PLL backbone and PEG strands. This modification was done alone or in combination with an azide end on the PEG strands that enabled in situ conjugations of adhesion peptides or fluorescent labels (by a simple application of commercially available molecules for copper-free click chemistry compatible with cell survival). To balance the functional (adhesion-promoting) vs cell-repellent copolymers, mixed layers of adjusted compositions were obtained by coadsorption from mixed solutions of the cleavable copolymer with noncleavable and repellant PLL-g-PEG. The deposition of copolymers and quantitative cleavage as triggered by reductive conditions (application of solutions of tris(carboxyethyl)phosphine, dithiothreitol, or glutathione) were characterized by QCM-D, XPS, and fluorescence microscopy. In cell culture conditions, redox-triggered cleavage was obtained by a nontoxic application of TCEP for a few minutes, enabling either to release cell attachment points (i.e., cleavage of RGD-presenting areas) or to "open" nonspecific adherent areas (i.e., transition from PEG-presenting areas to adherent PLL-like coatings).
引用
收藏
页码:4367 / 4376
页数:10
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