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A multi-cellular 3D bioprinting approach for vascularized heart tissue engineering based on HUVECs and iPSC-derived cardiomyocytes

机译:基于HUVEC和iPSC衍生的心肌细胞用于血管化心脏组织工程的多细胞3D生物打印方法

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摘要

The myocardium behaves like a sophisticated orchestra that expresses its true potential only if each member performs the correct task harmonically. Recapitulating its complexity within engineered 3D functional constructs with tailored biological and mechanical properties, is one of the current scientific priorities in the field of regenerative medicine and tissue engineering. In this study, driven by the necessity of fabricating advanced model of cardiac tissue, we present an innovative approach consisting of heterogeneous, multi-cellular constructs composed of Human Umbilical Vein Endothelial Cells (HUVECs) and induced pluripotent cell-derived cardiomyocytes (iPSC-CMs). Cells were encapsulated within hydrogel strands containing alginate and PEG-Fibrinogen (PF) and extruded through a custom microfluidic printing head (MPH) that allows to precisely tailor their 3D spatial deposition, guaranteeing a high printing fidelity and resolution. We obtained a 3D cardiac tissue compose of iPSC-derived CMs with a high orientation index imposed by the different defined geometries and blood vessel-like shapes generated by HUVECs which, as demonstrated by in vivo grafting, better support the integration of the engineered cardiac tissue with host’s vasculature.
机译:心肌的行为就像一个复杂的乐团,只有在每个成员和谐地执行正确的任务时,它才能表达其真正的潜力。在具有定制的生物学和机械特性的工程3D功能结构中概括其复杂性,是再生医学和组织工程领域当前的科学重点之一。在这项研究中,受制于先进的心脏组织模型的推动,我们提出了一种创新的方法,该方法由人脐静脉内皮细胞(HUVEC)和诱导性多能细胞衍生的心肌细胞(iPSC-CM)组成的异质,多细胞构建体组成)。细胞被封装在包含藻酸盐和PEG-纤维蛋白原(PF)的水凝胶链中,并通过定制的微流体印刷头(MPH)挤出,从而可以精确地定制其3D空间沉积,从而确保高印刷保真度和分辨率。我们获得了由iPSC衍生的CM组成的3D心脏组织,其高定向指数由HUVEC产生的不同定义的几何形状和血管样形状所强加,如体内移植所证明的那样,它可以更好地支持工程化心脏组织的整合与宿主的脉管系统。

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