Bioengineering Vascular Networks to Study Angiogenesis and Vascularization of Physiologically Relevant Tissue Models in Vitro

被引:37
作者
Dikici, Serkan [1 ]
Claeyssens, Frederik [1 ]
MacNeil, Sheila [1 ]
机构
[1] Univ Sheffield, Kroto Res Inst, Dept Mat Sci & Engn, Sheffield S3 7HQ, S Yorkshire, England
基金
英国工程与自然科学研究理事会; 英国医学研究理事会;
关键词
angiogenesis; vascularization; 3D model; angiogenesis model; tissue engineering; skin; tissue-engineered skin model; ENDOTHELIAL GROWTH-FACTOR; BASEMENT-MEMBRANE; ENGINEERED SKIN; ELECTROSPUN SCAFFOLDS; ALGINATE HYDROGELS; VIVO EXPRESSION; CELLS; VEGF; SIMILARITIES; PROGRESSION;
D O I
10.1021/acsbiomaterials.0c00191
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Angiogenesis assays are essential for studying aspects of neovascularization and angiogenesis and investigating drugs that stimulate or inhibit angiogenesis. To date, there are several in vitro and in vivo angiogenesis assays that are used for studying different aspects of angiogenesis. Although in vivo assays are the most representative of native angiogenesis, they raise ethical questions, require considerable technical skills, and are expensive. In vitro assays are inexpensive and easier to perform, but the majority of them are only two-dimensional cell monolayers which lack the physiological relevance of three-dimensional structures. Thus, it is important to look for alternative platforms to study angiogenesis under more physiologically relevant conditions in vitro. Accordingly, in this study, we developed polymeric vascular networks to be used to study angiogenesis and vascularization of a 3D human skin model in vitro. Our results showed that this platform allowed the study of more than one aspect of angiogenesis, endothelial migration and tube formation, in vitro when combined with Matrigel. We successfully reconstructed a human skin model, as a representative of a physiologically relevant and complex structure, and assessed the suitability of the developed in vitro platform for studying endothelialization of the tissue-engineered skin model.
引用
收藏
页码:3513 / 3528
页数:16
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