共 43 条
Two-tier hydrogel degradation to boost endothelial cell morphogenesis
被引:58
作者:

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Levental, Kandice R.
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机构: Max Bergmann Ctr Biomat Dresden MBC, Leibniz Inst Polymer Res Dresden IPF, D-01069 Dresden, Germany

Tsurkan, Mikhail V.
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机构: Max Bergmann Ctr Biomat Dresden MBC, Leibniz Inst Polymer Res Dresden IPF, D-01069 Dresden, Germany

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Freudenberg, Uwe
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机构: Max Bergmann Ctr Biomat Dresden MBC, Leibniz Inst Polymer Res Dresden IPF, D-01069 Dresden, Germany

Werner, Carsten
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h-index: 0
机构:
Max Bergmann Ctr Biomat Dresden MBC, Leibniz Inst Polymer Res Dresden IPF, D-01069 Dresden, Germany Max Bergmann Ctr Biomat Dresden MBC, Leibniz Inst Polymer Res Dresden IPF, D-01069 Dresden, Germany
机构:
[1] Max Bergmann Ctr Biomat Dresden MBC, Leibniz Inst Polymer Res Dresden IPF, D-01069 Dresden, Germany
关键词:
Angiogenesis;
Hydrogel;
Degradation;
Endothelial cell;
Matrix metalloproteinase;
PLASMINOGEN ACTIVATORS;
EXTRACELLULAR-MATRIX;
BASEMENT-MEMBRANE;
SYNTHETIC MATRIX;
GROWTH;
MIGRATION;
ADHESION;
VEGF;
DIFFERENTIATION;
ANGIOGENESIS;
D O I:
10.1016/j.biomaterials.2011.08.078
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:
Cell-responsive degradation of biofunctional scaffold materials is required in many tissue engineering strategies and commonly achieved by the incorporation of protease-sensitive oligopeptide units. In extension of this approach, we combined protease-sensitive and -insensitive cleavage sites for the far-reaching control over degradation rates of starPEG-heparin hydrogel networks with orthogonally modulated elasticity, RGD presentation and VEGF delivery. Enzymatic cleavage was massively accelerated when the accessibility of the gels for proteases was increased through non-enzymatic cleavage of ester bonds. The impact of gel susceptibility to degradation was explored for the 3-dimensional ingrowth of human endothelial cells. Gels with accelerated degradation and VEGF release resulted in strongly enhanced endothelial cell invasion in vitro as well as blood vessel density in the chicken chorioallantoic membrane assay in vivo. Thus, combination of protease-sensitive and -insensitive cleavage sites can amplify the degradation of bioresponsive gel materials in ways that boost endothelial cell morphogenesis. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:9649 / 9657
页数:9
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