双3D打印用于血管化骨组织再生

Sung Yun Hann, H. Cui, Timothy Esworthy, Xuan Zhou, Se-jun Lee, M. Plesniak, Lijie Grace Zhang
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引用次数: 43

摘要

足够的血管网络的发展对于成功制造用于再生医学的组织结构至关重要,因为血管化对于执行组织的代谢功能至关重要,例如营养物质的运输和废物的清除。近年来,由于骨骼疾病和缺陷对社会老一辈的影响显著,3D打印血管化骨的努力得到了大量关注。然而,传统的和以前的3D打印骨研究一直受到难以获得纳米级几何精度以重现天然骨的独特特征的困扰。此外,发展真正的仿生血管化骨组织的过程在历史上一直是复杂的。在这项研究中,利用简单立体光刻(SLA)和熔融沉积建模(FDM) 3D打印系统的结合,开发了一种具有可灌注、内皮化血管通道的仿生纳米骨组织结构。使用FDM打印聚乙烯醇(PVA)牺牲模板在SLA打印骨支架内创建可灌注血管通道。在人造结构中,通过人骨髓间充质干细胞(hMSCs)的成骨分化形成骨组织,并且在人脐静脉内皮细胞(HUVECs)灌注后,通过内皮化血管通道的血管生成萌发出独特的毛细血管。此外,在生理相关的培养条件下,对制备的构建体进行了评估,以预测植入人体后的组织发育。实验结果显示,定制设计的生物反应器与hMSC-HUVEC共培养系统促进了血管网络的形成和构建体的成骨成熟,观察时间长达20天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual 3D Printing for Vascularized Bone Tissue Regeneration
The development of sufficient vascular networks is crucial for the successful fabrication of tissue constructs for regenerative medicine, as vascularization is essential to perform the metabolic functions of tissues, such as nutrient transportation and waste removal. In recent years, efforts to 3D print vascularized bone have gained substantial attention, as bone disorders and defects have a marked impact on the older generations of society. However, conventional and previous 3D printed bone studies have been plagued by the difficulty in obtaining the nanoscale geometrical precision necessary to recapitulate the distinct characteristics of natural bone. Additionally, the process of developing truly biomimetic vascularized bone tissue has been historically complex. In this study, a biomimetic nano-bone tissue construct with a perfusable, endothelialized vessel channel was developed using a combination of simple stereolithography (SLA) and fused deposition modeling (FDM) 3D printing systems. The perfusable vessel channel was created within the SLA printed bone scaffold using an FDM printed polyvinyl alcohol (PVA) sacrificial template. Within the fabricated constructs, bone tissue was formed through the osteogenic differentiation of human bone marrow mesenchymal stem cells (hMSCs), and distinct capillaries sprouted through the angiogenesis of the endothelialized vessel channel after human umbilical vein endothelial cells (HUVECs) had been perfused throughout. Furthermore, the fabricated constructs were evaluated in physiologically relevant culture conditions to predict tissue development after implantation in the human body. The experimental results revealed that the custom-designed bioreactor with an hMSC-HUVEC co-culture system enhanced the formation of vascular networks and the osteogenic maturation of the constructs for up to 20 days of observation.
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