Layer-by-Layer Films Made from Extracellular Matrix Macromolecules on Silicone Substrates

被引:46
作者
Mhanna, Rami F. [1 ]
Voeroes, Janos [1 ]
Zenobi-Wong, Marcy [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Biomed Engn, Lab Biosensors & Bioelect, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
POLYELECTROLYTE MULTILAYER FILMS; ATOMIC-FORCE MICROSCOPY; BIOMEDICAL APPLICATIONS; SURFACE MODIFICATION; CHONDROITIN SULFATE; CELL-ADHESION; ARTICULAR-CARTILAGE; COLLAGEN FIBRILS; HYALURONIC-ACID; OXYGEN PLASMA;
D O I
10.1021/bm1012772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The layer-by-layer (LbL) technique has been widely used to produce nanofilms for biomedical applications. Naturally occurring polymers such as ECM macromolecules are attractive candidates for LbL film preparation. In this study, we assessed the build-up of type I collagen (Col1)/chondroitin sulfate (CS) or Col1/Heparin (HN) on polydimethylsiloxane (PDMS) substrates. The build-up was assessed by quartz crystal microbalance with dissipation (QCM-D) and atomic force microscopy (AFM). Integrin-mediated cell adhesion was assessed by studying the cytoskeletal organization of mammalian primary cells (chondrocytes) seeded on different end layers and number of layers. Data generated from the QCM-D observations showed a consistent build-up of films with more adsorption in the case of Col1/HN. Col1/CS films were stable in media, whereas Col1/HN films were not. AFM analysis showed that the layers were fibrillar in structure for both systems and between 20 and 30 nm thick. The films promoted cell adhesion when compared with tissue culture plastic in serum-free media with cycloheximide. Crosslinking of the films resulted in constrained cell spreading and a ruffled morphology. Finally, betal integrin blocking antibodies prevented cell spreading, suggesting that cell adhesion and spreading were mediated mainly by interaction with the collagen fibrils. The ability to construct stable ECM-based films on PDMS has particular relevance in mechanobiology, microfluidics, and other biomedical applications.
引用
收藏
页码:609 / 616
页数:8
相关论文
共 44 条
[1]   Modification of polysiloxane polymers for biomedical applications: a review [J].
Abbasi, F ;
Mirzadeh, H ;
Katbab, AA .
POLYMER INTERNATIONAL, 2001, 50 (12) :1279-1287
[2]   Biomedical applications of electrostatic layer-by-layer nano-assembly of polymers, enzymes, and nanoparticles [J].
Ai, H ;
Jones, SA ;
Lvov, YM .
CELL BIOCHEMISTRY AND BIOPHYSICS, 2003, 39 (01) :23-43
[3]   Involvement of reactive oxygen species in cyclic stretch-induced NF-κB activation in human fibroblast cells [J].
Amma, H ;
Naruse, K ;
Ishiguro, N ;
Sokabe, M .
BRITISH JOURNAL OF PHARMACOLOGY, 2005, 145 (03) :364-373
[4]   Hydrophilization and hydrophobic recovery of PDMS by oxygen plasma and chemical treatment - An SEM investigation [J].
Bodas, Dhananjay ;
Khan-Malek, Chantal .
SENSORS AND ACTUATORS B-CHEMICAL, 2007, 123 (01) :368-373
[5]   Multiple Functionalities of Polyelectrolyte Multilayer Films: New Biomedical Applications [J].
Boudou, Thomas ;
Crouzier, Thomas ;
Ren, Kefeng ;
Blin, Guillaume ;
Picart, Catherine .
ADVANCED MATERIALS, 2010, 22 (04) :441-467
[6]   Polyelectrolyte multilayer films with pegylated polypeptides as a new type of anti-microbial protection for biomaterials [J].
Boulmedais, F ;
Frisch, B ;
Etienne, O ;
Lavalle, P ;
Picart, C ;
Ogier, J ;
Voegel, JC ;
Schaaf, P ;
Egles, C .
BIOMATERIALS, 2004, 25 (11) :2003-2011
[7]   A CLINICAL AND IMMUNOLOGICAL EVALUATION OF WOMEN WITH SILICONE BREAST IMPLANTS AND SYMPTOMS OF RHEUMATIC DISEASE [J].
BRIDGES, AJ ;
CONLEY, C ;
WANG, G ;
BURNS, DE ;
VASEY, FB .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (12) :929-936
[8]   Interaction of polyelectrolytes and their composites with living cells [J].
Chanana, M ;
Gliozzi, A ;
Diaspro, A ;
Chodnevskaja, I ;
Huewel, S ;
Moskalenko, V ;
Ulrichs, K ;
Galla, HJ ;
Krol, S .
NANO LETTERS, 2005, 5 (12) :2605-2612
[9]   Fuzzy nanoassemblies: Toward layered polymeric multicomposites [J].
Decher, G .
SCIENCE, 1997, 277 (5330) :1232-1237
[10]   DNA-based formation of a supported, three-dimensional lipid vesicle matrix probed by QCM-D and SPR [J].
Granéli, A ;
Edvardsson, M ;
Höök, F .
CHEMPHYSCHEM, 2004, 5 (05) :729-733