| Literature DB >> 24695092 |
Christopher M Walthers1, Alireza K Nazemi1, Shilpy L Patel1, Benjamin M Wu2, James C Y Dunn3.
Abstract
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-μm 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.Entities:
Keywords: Angiogenesis; Polycaprolactone; Porosity; Smooth muscle constructs; Tissue engineering
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Year: 2014 PMID: 24695092 PMCID: PMC4018739 DOI: 10.1016/j.biomaterials.2014.03.025
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479