Recombinant Spider Silk Functionalized with a Motif from Fibronectin Mediates Cell Adhesion and Growth on Polymeric Substrates by Entrapping Cells During Self-Assembly

被引:14
作者
Tasiopoulos, Christos Panagiotis [1 ]
Widhe, Mona [1 ]
Hedhammar, My [1 ]
机构
[1] KTH Royal Inst Technol, AlbaNova Univ Ctr, Div Prot Sci, Sch Engn Sci Chem Biotechnol & Hlth, S-11421 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
cell seeding; recombinant spider silk; RGD binding motif; surface functionalization; revascularization applications; VASCULAR GRAFTS; EXTRACELLULAR-MATRIX; IN-VITRO; ENDOTHELIALIZATION; PROLIFERATION; STRATEGIES; IMPLANTS; HEPARIN;
D O I
10.1021/acsami.8b02647
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In vitro endothelialization of synthetic grafts or engineered vascular constructs is considered a promising alternative to overcome shortcomings in the availability of autologous vessels and in graft complications with synthetics. A number of cell-seeding techniques have been implemented to render vascular grafts accessible for cells to attach, proliferate, and spread over the surface area. Nonetheless, seeding efficiency and the time needed for cells to adhere varies dramatically. Herein, we investigated a novel cell-seeding approach (denoted co-seeding) that enables cells to bind to a motif from fibronectin included in a recombinant spider silk protein. Entrapment of cells occurs at the same time as the silk assembles into a nanofibrillar coating on various substrates. Cell adhesion analysis showed that the technique can markedly improve cell-seeding efficiency to nonfunctionalized polystyrene surfaces, as well as establish cell attachment and growth of human dermal microvascular endothelial cells on bare polyethylene terephthalate and polytetrafluoroethylene (PTFE) substrates. Scanning electron microscopy images revealed a uniform endothelial cell layer and cell-substratum compliance with the functionalized silk protein to PTFE surfaces. The co-seeding technique holds a great promise as a method to reliably and quickly cellularize engineered vascular constructs as well as to in vitro endothelialize commercially available cardiovascular grafts.
引用
收藏
页码:14531 / 14539
页数:9
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