Fibronectin-mediated endothelialisation of chitosan porous matrices

被引:34
作者
Amaral, Isabel F. [1 ]
Unger, Ronald E. [2 ]
Fuchs, Sabine [2 ]
Mendonca, Ana M. [3 ]
Sousa, Susana R. [1 ,4 ]
Barbosa, Mario A. [1 ]
Pego, Ana P. [1 ]
Kirkpatrick, C. J. [2 ]
机构
[1] Univ Porto, Div Biomat, INEB, P-4150180 Oporto, Portugal
[2] Johannes Gutenberg Univ Mainz, Inst Pathol, REPAIR Lab, D-55101 Mainz, Germany
[3] Univ Porto, Fac Engn, Div Sinal & Imagem, INEB, P-4200465 Oporto, Portugal
[4] Inst Super Engn Porto, Dep Engn Quim, P-4200465 Oporto, Portugal
关键词
Chitin/chitosan; Endothelial cell; Angiogenesis; Fibronectin; Protein adsorption; Scaffold; HUMAN OSTEOBLASTIC CELLS; IN-VITRO; INTEGRIN BINDING; GROWTH; CHITIN; ADSORPTION; SCAFFOLDS; ADHESION; FILMS; VASCULARIZATION;
D O I
10.1016/j.biomaterials.2009.06.056
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Chitosan (Ch) porous matrices were investigated regarding their ability to be colonized by human microvascular endothelial cells (HPMEC-ST1.6R cell line) and macrovascular endothelial cells namely HUVECs. Specifically we assessed if previous incubation of Ch in a fibronectin (FN) solution was effective in promoting endothelial cell (EC) adhesion to Ch matrices with different degrees of acetylation (DAs). Upon FN physiadsorption, marked differences were found between the two DAs investigated, namely DA 4% and 15%. While cell adhesion was impaired on Ch with DA 15%, ECs were able to not only adhere to Ch with DA 4%, but also to spread and colonize the scaffolds, with retention of the EC phenotype and angiogenic potential. To explain the observed differences between the two DAs, protein adsorption studies using I-125-FN and immunofluorescent labelling of FN cell-binding domains were carried out. in agreement with the higher cell numbers found, scaffolds with DA 4% revealed a higher number of exposed FN cell-binding domains as well as greater ability to adsorb FN and to retain and exchange adsorbed FN in the presence of competitive proteins. These findings suggest that the DA is a key parameter modulating EC adhesion to FN-coated Ch by influencing the adsorbed protein layer. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5465 / 5475
页数:11
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