Cardiac muscle tissue engineering: toward an in vitro model for electrophysiological studies

被引:253
作者
Bursac, N
Papadaki, M
Cohen, RJ
Schoen, FJ
Eisenberg, SR
Carrier, R
Vunjak-Novakovic, G
Freed, LE
机构
[1] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[3] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1999年 / 277卷 / 02期
关键词
myocyte; impulse propagation; electrophysiology; three-dimensional;
D O I
10.1152/ajpheart.1999.277.2.H433
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective of this study was to establish a three-dimensional (3-D) in vitro model system of cardiac muscle for electrophysiological studies. Primary neonatal rat ventricular cells containing lower or higher fractions of cardiac myocytes were cultured on polymeric scaffolds in bioreactors to form regular or enriched cardiac muscle constructs, respectively. After 1 wk, all constructs contained a peripheral tissue-like region (50-70 mu m thick) in which differentiated cardiac myocytes were organized in multiple layers in a 3-D configuration. Indexes of cell size (protein/DNA) and metabolic activity (tetrazolium conversion/DNA) were similar for constructs and neonatal rat ventricles. Electrophysiological studies conducted using a linear array of extracellular electrodes showed that the peripheral region of constructs exhibited relatively homogeneous electrical properties and sustained macroscopically continuous impulse propagation on a centimeter-size scale. Electrophysiological properties of enriched constructs were superior to those of regular constructs but inferior to those of native ventricles. These results demonstrate that 3-D cardiac muscle constructs can be engineered with cardiac-specific structural and electrophysiological properties and used for in vitro impulse propagation studies.
引用
收藏
页码:H433 / H444
页数:12
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