Directional migration of endothelial cells towards angiogenesis using polymer fibres in a 3D co-culture system

被引:57
作者
Hadjizadeh, Afra [1 ]
Doillon, Charles J. [2 ,3 ]
机构
[1] Univ Sherbrooke, Dept Chem Engn & Biotechnol, Sherbrooke, PQ J1K 2R1, Canada
[2] CHULs Res Ctr, Oncol & Mol Endocrinol Res Ctr, Quebec City, PQ G1K 7P4, Canada
[3] Univ Laval, Fac Med, Dept Surg, Quebec City, PQ G1K 7P4, Canada
关键词
surface-modified polymer fibres; prevascularized tissue construct; human umbilical vein endothelial cells; directional microvessel; bioactive; angiogenesis; IN-VITRO MODELS; EXTRACELLULAR-MATRIX; PROGENITOR CELLS; FIBRIN MATRICES; TISSUE; GROWTH; SCAFFOLDS; REGENERATION; VASCULARIZATION; VASCULOGENESIS;
D O I
10.1002/term.269
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Development of an in vitro prevascularized scaffold is of great importance to produce vascularization in tissue-engineered devices and for other clinical purposes. To this aim, polymer fibres covered with human umbilical vein endothelial cells (HUVECs) were used to induce directional 'angiogenesis' in a 3D co-culture system. Gelatin or RGD peptides were immobilized on surface-modified polymer fibres [100 mu m diameter poly(ethylene terephthalate) monofilaments] via N-hepthylamine plasma polymer and carboxy-methyl-dextran interlayers. Fibres fully covered with HUVECs were then embedded in a fibrin gel, following a parallel alignment pattern, in the presence of fibroblasts. Tube-like structures occurred along the fibres and a network was formed between neighbouring fibres. These events were promoted with increased incubation times. Biomolecule-grafted fibres created a guidance pathway that facilitated coated endothelial cells to form lumens and, from them, sprouting processes. However, there were no significant differences between the different surface modifications on fibres in terms of promoting tube-like structures. Thus, different stages of angiogenesis can be initiated and guided using HUVECs precovered polymer fibres embedded in a soft supportive matrix, such as fibrin, which can be further applied to the development of in vitro prevascularized tissue-engineered scaffolds. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:524 / 531
页数:8
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