Mediating specific cell adhesion to low-adhesive diblock copolymers by instant modification with cyclic RGD peptides

被引:57
作者
Lieb, E
Hacker, M
Tessmar, J
Kunz-Schughart, LA
Fiedler, J
Dahmen, C
Hersel, U
Kessler, H
Schulz, MB
Göpferich, A
机构
[1] Univ Regensburg, Dept Pharmaceut Technol, D-93040 Regensburg, Germany
[2] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[3] Univ Regensburg, Inst Pathol, D-93053 Regensburg, Germany
[4] Univ Ulm, Dept Orthoped, Div Biochem Joint & Connect Tissue Dis, D-89081 Ulm, Germany
[5] Tech Univ Munich, Dept Organ Chem Biochem, D-85747 Garching, Germany
[6] Graz Univ, Inst Pharmaceut Sci Pharmaceut Technol, A-8010 Graz, Austria
关键词
cell adhesion; RGD peptide; integrin; osteoblast; surface modification; biomimetic material; poly(lactic acid); poly(ethylene oxide); diblock copolymer;
D O I
10.1016/j.biomaterials.2004.07.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
One promising strategy to control the interactions between biomaterial surfaces and attaching cells involves the covalent grafting of adhesion peptides to polymers on which protein adsorption, which mediates unspecific cell adhesion, is essentially suppressed. This study demonstrates a surface modification concept for the covalent anchoring of RGD peptides to reactive diblock copolymers based on monoamine poly(ethylene glycol)-block-POIY(D,L-lactic acid) (H2N-PEG-PLA). Films of both the amine-reactive (ST-NHPEG(2)PLA(20)) and the thiol-reactive derivative (MP-NH-PEG(2)PLA(40)) were modified with cyclic alphavbeta3/alphavbeta5 integrin subtype specific RGD peptides simply by incubation of the films with buffered solutions of the peptides. Human osteoblasts known to express these integrins were used to determine cell-polymer interactions. The adhesion experiments revealed significantly increased cell numbers and cell spreading on the RGD-modified surfaces mediated by RGD-integrin-interactions. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2333 / 2341
页数:9
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