Center for Bionics, Biomedical Research Institute, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea; Department of Maxillofacial Biomedical Engineering and Institute of Oral Biology, School of Dentistry, Kyung Hee University, Seoul 130-701, Republic of Korea.
Center for Bionics, Biomedical Research Institute, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea.
J Biomech. 2014 Jan 22;47(2):400-9. doi: 10.1016/j.jbiomech.2013.11.013. Epub 2013 Dec 2.
Conventional cardiac physiology experiments investigate in vitro beat frequency using cells isolated from adult or neonatal rat hearts. In this study, we show that various cantilever shapes and drug treatments alter cardiomyocyte contraction force in vitro. Four types of cantilevers were used to compare the contractile forces: flat, peg patterned, grooved, and peg and grooved. Contraction force was represented as bending deflection of the cantilever end. The deflections of the flat, peg patterned, grooved, and peg and grooved cantilevers were 24.2 nN, 41.6 nN, 121 nN, and 134.2 nN, respectively. We quantified the effect of drug treatments on cardiomyocyte contractile forces on the grooved cantilever using Digoxin, Isoproterenol, and BayK8644, all of which increase contractile force, and Verapamil, which decreases contractile force. The cardiomyocyte contractile force without drugs decreased 8 days after culture initiation. Thus, we applied Digoxin, Isoproterenol, and BayK8644 at day 8, and Verapamil at day 5. Digoxin, Isoproterenol, and BayK8644 increased the cardiomyocyte contractile forces by 19.31%, 9.75%, and 23.81%, respectively. Verapamil decreased the contraction force by 48.06%. In summary, contraction force changes in response to adhesion surface topology and various types of drug treatments. We observed these changes by monitoring cell alignment, adhesion, morphology, and bending displacement with cantilever sensors.
传统的心脏生理学实验使用从成年或新生大鼠心脏中分离的细胞在体外研究跳动频率。在这项研究中,我们表明,各种悬臂形状和药物处理会改变体外心肌细胞的收缩力。使用了四种类型的悬臂来比较收缩力:平板、钉状图案、凹槽和钉状和凹槽。收缩力表示为悬臂末端的弯曲挠度。平板、钉状图案、凹槽和钉状和凹槽悬臂的挠度分别为 24.2 nN、41.6 nN、121 nN 和 134.2 nN。我们使用地高辛、异丙肾上腺素和 BayK8644 量化了药物处理对凹槽悬臂上心肌细胞收缩力的影响,所有这些药物都增加了收缩力,而维拉帕米则降低了收缩力。没有药物的心肌细胞收缩力在培养开始后 8 天下降。因此,我们在第 8 天施加地高辛、异丙肾上腺素和 BayK8644,在第 5 天施加维拉帕米。地高辛、异丙肾上腺素和 BayK8644 分别使心肌细胞收缩力增加了 19.31%、9.75%和 23.81%。维拉帕米使收缩力降低了 48.06%。总之,收缩力会因粘附表面拓扑和各种类型的药物处理而发生变化。我们通过使用悬臂传感器监测细胞对齐、粘附、形态和弯曲位移来观察这些变化。