Inadequate Processing of Decellularized Dermal Matrix Reduces Cell Viability In Vitro and Increases Apoptosis and Acute Inflammation In Vivo

被引:22
|
作者
Morris, Aaron H. [1 ,2 ]
Chang, Julie [1 ]
Kyriakides, Themis R. [1 ,2 ,3 ]
机构
[1] Yale Univ, Dept Biomed Engn, New Haven, CT USA
[2] Yale Univ, Dept Vasc Biol & Therapeut Program, New Haven, CT USA
[3] Yale Univ, Dept Pathol, New Haven, CT 06519 USA
来源
BIORESEARCH OPEN ACCESS | 2016年 / 5卷 / 01期
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
biomaterials; extracellular matrix; inflammation; tissue engineering;
D O I
10.1089/biores.2016.0021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Decellularized tissue scaffolds are commonly used in the clinic because they can be used as substitutes for more traditional biomaterials, while imparting additional physiological effects. Nevertheless, reports of complications associated with their use are widespread and poorly understood. This study probes possible causes of these complications by examining cell viability and apoptosis in response to eluents from decellularized dermis. Using multiple sources of decellularized dermis, this study shows that typical decellularized scaffolds (prepared with commonly used laboratory techniques, as well as purchased from commercial sources) contain soluble components that are cytotoxic and that these components can be removed by extensive washes in cell culture media. In addition, this study demonstrates that these observed in vitro phenotypes correlate with increased apoptosis and acute inflammation when implanted subcutaneously in mice.
引用
收藏
页码:177 / 187
页数:11
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