SEMM, European School of Molecular Medicine, Campus IFOM-IEO, Via Adamello 16, 20139 Milano, Italy; Fondazione Filarete, Viale Ortles 22/4, 20139 Milano, Italy.
Fondazione Filarete, Viale Ortles 22/4, 20139 Milano, Italy.
Biomaterials. 2015 Mar;45:124-31. doi: 10.1016/j.biomaterials.2014.12.031. Epub 2015 Jan 29.
Despite significant progresses were achieved in tissue engineering over the last 20 years, a number of unsolved problems still remain. One of the most relevant issues is the lack of a proper vascularization that is limiting the size of the engineered tissues to smaller than clinically relevant dimensions. Sacrificial molding holds great promise to engineered construct with perfusable vascular architectures, but there is still the need to develop more versatile approaches able to be independent of the nature and dimensions of the construct. In this work we developed a versatile sacrificial molding technique for fabricating bulk, cell-laden and porous scaffolds with embedded vascular fluidic networks. These branched fluidic architectures are created by highly resistant thermoplastic sacrificial templates, made of poly(vinyl alcohol), representing a remarkable progress in manufacturability and scalability. The obtained architecture, when perfused in bioreactor, has shown to prevent the formation of a necrotic core in thick cell-laden constructs and enabled the rapid fabrication of hierarchically branched endothelium. In conclusion we demonstrate a novel strategy towards the engineering of vascularized thick tissues through the integration of the PVA-based microfabrication sacrificial approach and perfusion bioreactors. This approach may be able to scale current engineered tissues to clinically relevant dimensions, opening the way to their widespread clinical applications.
尽管在过去的 20 年中,组织工程已经取得了重大进展,但仍有许多未解决的问题。其中最相关的问题之一是缺乏适当的血管化,这限制了工程组织的尺寸小于临床相关的尺寸。牺牲模塑在具有可灌注血管结构的工程构建体中具有很大的潜力,但仍需要开发更多能够独立于构建体的性质和尺寸的多功能方法。在这项工作中,我们开发了一种通用的牺牲模塑技术,用于制造具有嵌入式血管流形网络的大块、细胞负载和多孔支架。这些分支流形结构是由高度耐溶剂的热塑性牺牲模板制成的,这些模板由聚乙烯醇制成,这在制造和可扩展性方面取得了显著进展。在生物反应器中灌注时,所获得的结构显示出可以防止在厚细胞负载构建体中形成坏死核心,并能够快速制造出分层分支的内皮。总之,我们通过整合基于 PVA 的微加工牺牲方法和灌注生物反应器,展示了一种用于血管化厚组织工程的新策略。这种方法可以将当前的工程组织扩展到临床相关的尺寸,为其广泛的临床应用开辟了道路。