Sarig Udi, Nguyen Evelyne Bao-Vi, Wang Yao, Ting Sherwin, Bronshtein Tomer, Sarig Hadar, Dahan Nitsan, Gvirtz Maskit, Reuveny Shaul, Oh Steve K W, Scheper Thomas, Boey Yin Chiang Freddy, Venkatraman Subbu S, Machluf Marcelle
1 The Laboratory of Cancer Drug Delivery & Mammalian Cell Technology, Faculty of Biotechnology and Food Engineering, Technion-Israel Institute of Technology , Haifa, Israel .
Tissue Eng Part A. 2015 May;21(9-10):1507-19. doi: 10.1089/ten.tea.2014.0477. Epub 2015 Mar 19.
Functional vascularization is a prerequisite for cardiac tissue engineering of constructs with physiological thicknesses. We previously reported the successful preservation of main vascular conduits in isolated thick acellular porcine cardiac ventricular ECM (pcECM). We now unveil this scaffold's potential in supporting human cardiomyocytes and promoting new blood vessel development ex vivo, providing long-term cell support in the construct bulk. A custom-designed perfusion bioreactor was developed to remodel such vascularization ex vivo, demonstrating, for the first time, functional angiogenesis in vitro with various stages of vessel maturation supporting up to 1.7 mm thick constructs. A robust methodology was developed to assess the pcECM maximal cell capacity, which resembled the human heart cell density. Taken together these results demonstrate feasibility of producing physiological-like constructs such as the thick pcECM suggested here as a prospective treatment for end-stage heart failure. Methodologies reported herein may also benefit other tissues, offering a valuable in vitro setting for "thick-tissue" engineering strategies toward large animal in vivo studies.
功能性血管化是构建具有生理厚度的心脏组织工程的先决条件。我们之前报道过在分离的厚层脱细胞猪心室细胞外基质(pcECM)中成功保留主要血管管道。我们现在揭示了这种支架在支持人类心肌细胞和促进体外新血管发育方面的潜力,在构建体主体中提供长期的细胞支持。开发了一种定制设计的灌注生物反应器,用于在体外重塑这种血管化,首次证明了体外功能性血管生成,不同阶段的血管成熟支持高达1.7毫米厚的构建体。开发了一种强大的方法来评估pcECM的最大细胞容量,其类似于人类心脏细胞密度。综合这些结果表明,生产类似生理结构的构建体是可行的,例如这里提出的厚层pcECM,作为终末期心力衰竭的一种前瞻性治疗方法。本文报道的方法也可能有益于其他组织,为针对大型动物体内研究的“厚组织”工程策略提供了一个有价值的体外环境。