Surface-induced changes in protein adsorption and implications for cellular phenotypic responses to surface interaction

被引:192
作者
Allen, LT
Tosetto, M
Miller, IS
O'Connor, DP
Penney, SC
Lynch, I
Keenan, AK
Pennington, SR
Dawson, KA
Gallagher, WM [1 ]
机构
[1] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Ctr Mol Med, Sch Biomol & Biomed Sci, Dublin 4, Ireland
[2] Univ Coll Dublin, Sch Chem & Chem Biol, Irish Ctr Colloid Sci & Biomat, Dublin 4, Ireland
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Ctr Mol Med, Sch Med & Med Sci,Proteome Res Ctr, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
surface hydrophobicity; protein adsorption; fibronectin; focal adhesion; cell signalling; cell migration;
D O I
10.1016/j.biomaterials.2006.01.019
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Understanding external factors that determine cellular phenotypic responses is of key interest in the field of biomaterials. Currently, material surface characteristics, protein adsorption and cellular phenotypic responses are all considered to be interrelated and ultimately determine the biocompatibility of materials. The exact nature of the relationship between these distinct, yet related, phenomena still remains to be elucidated. Through the use of a series of thermoresponsive N-isopropylacrylamide-based co-polymer films, we aimed to shed light on the relationship between surface hydrophobicity, protein adsorption and subsequent cellular response. Despite changes in co-polymer hydrophobicity mediated by altered ratios of constituent monomers, differential cellular response was only apparent in the presence of serum. Co-polymer films displayed alterations with respect to the amount of protein adsorbed on the surface, with individual serum proteins (albumin and fibronectin) displaying contrasting adsorption characteristics. Changes in protein adsorption corresponded to changes in cell adhesion, cytoskeletal organisation and cell morphology, as well as to changes in cell movement and intracellular signalling events. Examination of focal adhesion kinase (FAK), and extracellular signal-regulated kinase (ERK 1/2), important mediators of adhesion and growth factor-related signalling events, revealed a comparative reduction in phosphorylation of these signalling proteins in cells grown on co-polymers in comparison to those cultured on tissue culture polystyrene (TCP; used as a control surface). We also associated surface-mediated phenotypic alterations of cells grown on TCP and co-polymer films with particular changes in gene expression. These results indicate that cellular response to interaction with our series of co-polymer films is determined by the surface-adsorbed protein layer, which in turn is determined by the changing surface chemistry as the ratio of the co-monomers is altered. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3096 / 3108
页数:13
相关论文
共 62 条
[1]   An in vitro model for mineralization of human osteoblast-like cells on implant materials [J].
Ahmad, M ;
McCarthy, M ;
Gronowicz, G .
BIOMATERIALS, 1999, 20 (03) :211-220
[2]   Interaction of soft condensed materials with living cells: Phenotype/transcriptome correlations for the hydrophobic effect [J].
Allen, LT ;
Fox, EJP ;
Blute, I ;
Kelly, ZD ;
Rochev, Y ;
Keenan, AK ;
Dawson, KA ;
Gallagher, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6331-6336
[3]  
ANDRADE JD, 1986, ADV POLYM SCI, V79, P1
[4]  
[Anonymous], [No title captured]
[5]  
Aplin AE, 1999, J CELL SCI, V112, P695
[6]   Surface modifications and molecular imprinting of polymers in medical and pharmaceutical applications [J].
Bures, P ;
Huang, YB ;
Oral, E ;
Peppas, NA .
JOURNAL OF CONTROLLED RELEASE, 2001, 72 (1-3) :25-33
[7]   Focal adhesion kinase tyrosine-861 is a major site of phosphorylation by Src [J].
Calalb, MB ;
Zhang, XE ;
Polte, TR ;
Hanks, SK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 228 (03) :662-668
[8]   Rho-stimulated contractility drives the formation of stress fibers and focal adhesions [J].
ChrzanowskaWodnicka, M ;
Burridge, K .
JOURNAL OF CELL BIOLOGY, 1996, 133 (06) :1403-1415
[9]   Bi-directional signal transduction by integrin receptors [J].
Coppolino, MG ;
Dedhar, S .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (02) :171-188
[10]  
DAVIS RJ, 1993, J BIOL CHEM, V268, P14553