The effect of scaffold macroporosity on angiogenesis and cell survival in tissue-engineered smooth muscle

被引:66
|
作者
Walthers, Christopher M. [1 ]
Nazemi, Alireza K. [1 ]
Patel, Shilpy L. [1 ]
Wu, Benjamin M. [1 ,2 ]
Dunn, James C. Y. [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Adv Prosthodont Biomat & Hosp Dent, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Surg, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
Angiogenesis; Polycaprolactone; Porosity; Smooth muscle constructs; Tissue engineering; FIBROBLAST-GROWTH-FACTOR; IN-VIVO GROWTH; STEM-CELLS; POLYCAPROLACTONE SCAFFOLDS; ELECTROSPUN SCAFFOLDS; POLYMER-SCAFFOLDS; MECHANICAL STRAIN; POROUS SCAFFOLDS; VASCULARIZATION; DESIGN;
D O I
10.1016/j.biomaterials.2014.03.025
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Angiogenesis and survival of cells within thick scaffolds is a major concern in tissue engineering. The purpose of this study is to increase the survival of intestinal smooth muscle cells (SMCs) in implanted tissue-engineered constructs. We incorporated 250-mu m pores in multi-layered, electrospun scaffolds with a macroporosity ranging from 15% to 25% to facilitate angiogenesis. The survival of green fluorescent protein (GFP)-expressing SMCs was evaluated after 2 weeks of implantation. Whereas host cellular infiltration was similar in scaffolds with different macroporosities, blood vessel development increased with increasing macroporosity. Scaffolds with 25% macropores had the most GFP-expressing SMCs, which correlated with the highest degree of angiogenesis over 1 mm away from the outermost layer. The 25% macroporous group exceeded a critical threshold of macropore connectivity, accelerating angiogenesis and improving implanted cell survival in a tissue-engineered smooth muscle construct. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5129 / 5137
页数:9
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