Department of General and Interventional Cardiology, University Heart Center Hamburg, Martinistrasse 52, 20246, Hamburg, Germany.
DZHK (German Centre for Cardiovascular Research), Partner site Hamburg/Kiel/Lübeck, Hamburg, Germany.
Basic Res Cardiol. 2018 Sep 3;113(5):41. doi: 10.1007/s00395-018-0701-2.
Engineered heart tissue (EHT) from rat cells is a useful tool to study ventricular biology and cardiac drug safety. Since atrial and ventricular cells differ significantly, EHT and other 3D cell culture formats generated from ventricular cells have been of limited value to study atrial biology. To date, reliable in vitro models that reflect atrial physiology are lacking. Therefore, we established a novel EHT model using rat atrial cells (atrial EHT, aEHT) to assess atrial physiology, contractility and drug response. The tissue constructs were characterized with regard to gene expression, histology, electrophysiology, and the response to atrial-specific drugs. We observed typical functional properties of atrial tissue in our model such as more regular spontaneous beating with lower force, shorter action potential duration, and faster contraction and relaxation compared to ventricular EHT (vEHT). The expression of atrial-specific genes and proteins was high, whereas ventricle-specific transcripts were virtually absent. The atrial-selective drug carbachol had a strong negative inotropic and chronotropic effect on aEHT only. Taken together, the results demonstrate the feasibility of aEHT as a novel atrial 3D model and as a benchmark for tissue engineering with human induced pluripotent stem cell-derived atrial-like cardiomyocytes. Atrial EHT faithfully recapitulates atrial physiology and shall be useful to study atrial molecular physiology in health and disease as well as drug response.
工程化心脏组织(EHT)源自大鼠细胞,是研究心室生物学和心脏药物安全性的有用工具。由于心房和心室细胞存在显著差异,因此源自心室细胞的 EHT 和其他 3D 细胞培养形式对研究心房生物学的价值有限。迄今为止,缺乏可靠的反映心房生理学的体外模型。因此,我们使用大鼠心房细胞(心房 EHT,aEHT)建立了一种新型 EHT 模型,以评估心房生理学、收缩性和药物反应。我们从基因表达、组织学、电生理学以及对心房特异性药物的反应等方面对组织构建体进行了表征。与心室 EHT(vEHT)相比,我们在模型中观察到了典型的心房组织功能特性,例如自发性搏动更规则,收缩力更低,动作电位持续时间更短,收缩和舒张更快。心房特异性基因和蛋白质的表达水平较高,而心室特异性转录本几乎不存在。心房选择性药物卡巴胆碱仅对 aEHT 产生强烈的负性肌力和变时作用。总之,这些结果证明了 aEHT 作为一种新型 3D 心房模型的可行性,以及作为源自人诱导多能干细胞的心房样心肌细胞的组织工程学的基准的可行性。心房 EHT 忠实地再现了心房生理学,将有助于研究健康和疾病状态下的心房分子生理学以及药物反应。