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  • Perfusion-decellularized matrix: using nature's platform to engineer a bioartificial heart.

Perfusion-decellularized matrix: using nature's platform to engineer a bioartificial heart.

Nature medicine (2008-01-15)
Harald C Ott, Thomas S Matthiesen, Saik-Kia Goh, Lauren D Black, Stefan M Kren, Theoden I Netoff, Doris A Taylor
摘要

About 3,000 individuals in the United States are awaiting a donor heart; worldwide, 22 million individuals are living with heart failure. A bioartificial heart is a theoretical alternative to transplantation or mechanical left ventricular support. Generating a bioartificial heart requires engineering of cardiac architecture, appropriate cellular constituents and pump function. We decellularized hearts by coronary perfusion with detergents, preserved the underlying extracellular matrix, and produced an acellular, perfusable vascular architecture, competent acellular valves and intact chamber geometry. To mimic cardiac cell composition, we reseeded these constructs with cardiac or endothelial cells. To establish function, we maintained eight constructs for up to 28 d by coronary perfusion in a bioreactor that simulated cardiac physiology. By day 4, we observed macroscopic contractions. By day 8, under physiological load and electrical stimulation, constructs could generate pump function (equivalent to about 2% of adult or 25% of 16-week fetal heart function) in a modified working heart preparation.

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单克隆抗 肌动蛋白(α-肌节) 小鼠抗, clone 5C5, ascites fluid
Sigma-Aldrich
抗-血管性血友病因子 兔抗, IgG fraction of antiserum, buffered aqueous solution
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单克隆抗-连接蛋白-43 小鼠抗, clone CXN-6, ascites fluid