Strategies for improving the physiological relevance of human engineered tissues

被引:67
作者
Abbott, Rosalyn D. [1 ]
Kaplan, David L. [1 ]
机构
[1] Tufts Univ, Ctr Sci & Technol, Dept Biomed Engn, Medford, MA 02155 USA
基金
美国国家卫生研究院;
关键词
long-term culture; tissue engineering; microfluidics; 2D culture; 3D culture; bioreactors; MESENCHYMAL STEM-CELLS; LONG-TERM SURVIVAL; IN-VITRO; MICROFLUIDIC SYSTEM; PERFUSION CULTURE; CHONDROGENIC DIFFERENTIATION; MICROVASCULAR NETWORKS; EXTRACELLULAR-MATRIX; HUMAN OSTEOBLASTS; HUMAN HEPATOCYTES;
D O I
10.1016/j.tibtech.2015.04.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This review examines important robust methods for sustained, steady-state, in vitro culture. To achieve 'physiologically relevant' tissues in vitro additional complexity must be introduced to provide suitable transport, cell signaling, and matrix support for cells in 3D environments to achieve stable readouts of tissue function. Most tissue engineering systems draw conclusions on tissue functions such as responses to toxins, nutrition, or drugs based on short-term outcomes with in vitro cultures (2-14 days). However, short-term cultures limit insight with physiological relevance because the cells and tissues have not reached a steady-state.
引用
收藏
页码:401 / 407
页数:7
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