Radisic Milica, Park Hyoungshin, Shing Helen, Consi Thomas, Schoen Frederick J, Langer Robert, Freed Lisa E, Vunjak-Novakovic Gordana
Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, E25-342, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2004 Dec 28;101(52):18129-34. doi: 10.1073/pnas.0407817101. Epub 2004 Dec 16.
The major challenge of tissue engineering is directing the cells to establish the physiological structure and function of the tissue being replaced across different hierarchical scales. To engineer myocardium, biophysical regulation of the cells needs to recapitulate multiple signals present in the native heart. We hypothesized that excitation-contraction coupling, critical for the development and function of a normal heart, determines the development and function of engineered myocardium. To induce synchronous contractions of cultured cardiac constructs, we applied electrical signals designed to mimic those in the native heart. Over only 8 days in vitro, electrical field stimulation induced cell alignment and coupling, increased the amplitude of synchronous construct contractions by a factor of 7, and resulted in a remarkable level of ultrastructural organization. Development of conductive and contractile properties of cardiac constructs was concurrent, with strong dependence on the initiation and duration of electrical stimulation.
组织工程学的主要挑战在于引导细胞在不同层次尺度上构建被替代组织的生理结构和功能。要构建心肌组织,对细胞的生物物理调控需要重现天然心脏中存在的多种信号。我们假设,对正常心脏的发育和功能至关重要的心电-机械耦联决定了工程化心肌的发育和功能。为了诱导培养的心脏构建体同步收缩,我们施加了旨在模拟天然心脏电信号的电信号。仅在体外培养8天,电场刺激就诱导了细胞排列和耦联,使同步构建体收缩幅度增加了7倍,并导致了超微结构组织达到显著水平。心脏构建体的传导和收缩特性是同时发展的,强烈依赖于电刺激的起始和持续时间。