Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Japan.
Department of Cardiovascular Regenerative Medicine, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita 565-0871, Japan.
Biomaterials. 2014 Sep;35(27):7839-50. doi: 10.1016/j.biomaterials.2014.05.080. Epub 2014 Jun 20.
Engineering of three-dimensional (3D) cardiac tissues using decellularized extracellular matrix could be a new technique to create an "organ-like" structure of the heart. To engineer artificial hearts functionally comparable to native hearts, however, much remain to be solved including stable excitation-propagation. To elucidate the points, we examined conduction properties of engineered tissues. We repopulated the decellularized hearts with neonatal rat cardiac cells and then, we observed excitation-propagation of spontaneous beatings using high resolution cameras. We also conducted immunofluorescence staining to examine morphological aspects. Live tissue imaging revealed that GFP-labeled-isolated cardiac cells were migrated into interstitial spaces through extravasation from coronary arteries. Engineered hearts repopulated with Ca(2+)-indicating protein (GCaMP2)-expressing cardiac cells were subjected to optical imaging experiments. Although the engineered hearts generally showed well-organized stable excitation-propagation, the hearts also demonstrated arrhythmogenic propensity such as disorganized propagation. Immunofluorescence study revealed randomly-mixed alignment of cardiomyocytes, endothelial cells and smooth muscle cells. The recellularized hearts also showed disarray of cardiomyocytes and markedly decreased expression of connexin43. In conclusion, we successfully demonstrated that the recellularized hearts showed dynamic excitation-propagation as a "whole organ". Our strategy could provide prerequisite information to construct a 3D-engineered heart, functionally comparable to the native heart.
使用脱细胞细胞外基质工程化三维(3D)心脏组织可能是创建心脏“器官样”结构的新技术。然而,为了工程化出在功能上可与天然心脏相媲美的人工心脏,仍有许多问题亟待解决,包括稳定的兴奋传播。为了阐明这一点,我们检查了工程化组织的传导特性。我们用新生大鼠心脏细胞重新填充脱细胞心脏,然后使用高分辨率相机观察自发跳动的兴奋传播。我们还进行了免疫荧光染色以检查形态学方面。活体组织成像显示,GFP 标记的分离心脏细胞通过冠状动脉渗出从血管外渗到间质空间。用表达 Ca(2+)-指示蛋白(GCaMP2)的心脏细胞再填充的工程化心脏被用于光学成像实验。尽管工程化心脏通常表现出组织良好的稳定兴奋传播,但心脏也表现出心律失常倾向,如传播紊乱。免疫荧光研究显示,心肌细胞、内皮细胞和平滑肌细胞随机混合排列。再灌注心脏也显示出心肌细胞排列紊乱和连接蛋白 43 的表达明显减少。总之,我们成功地证明了再灌注心脏作为“整个器官”表现出动态兴奋传播。我们的策略可以为构建功能上可与天然心脏相媲美的 3D 工程化心脏提供必要的信息。