Department of Bioengineering, Clemson University, Clemson, South Carolina 29634-0905, USA.
Tissue Eng Part A. 2011 Jan;17(1-2):25-36. doi: 10.1089/ten.TEA.2010.0138. Epub 2010 Sep 6.
Tissue engineering holds great promise for treatment of valvular diseases. Despite excellent progress in the field, current approaches do not fully take into account each patient's valve anatomical uniqueness, the presence of a middle spongiosa cushion that allows shearing of external fibrous layers (fibrosa and ventricularis), and the need for autologous valvular interstitial cells. In this study we propose a novel approach to heart valve tissue engineering based on bioreactor conditioning of mesenchymal stem cell-seeded, valve-shaped constructs assembled from layered collagenous scaffolds. Fibrous scaffolds were prepared by decellularization of porcine pericardium and spongiosa scaffolds by decellularization and elastase treatment of porcine pulmonary arteries. To create anatomically correct constructs, we created silicone molds from native porcine aortic valves, dried two identical fibrous scaffolds onto the molds, and stabilized them with penta-galloyl-glucose a reversible collagen-binding polyphenol that reduces biodegradation. The layers were fused with a protein/aldehyde scaffold bio-adhesive and neutralized to reduce cytotoxicity. Spongiosa scaffolds, seeded with human bone marrow-derived stem cells, were inserted within the valve-shaped layered scaffolds and sutured inside the original aortic root. The final product was mounted in a heart valve bioreactor and cycled in cell culture conditions. Most cells were alive after 8 days, elongated significantly, and stained positive for vimentin, similar to native human valvular interstitial cells, indicating feasibility of our approach.
组织工程在治疗瓣膜疾病方面具有巨大的潜力。尽管该领域取得了优异的进展,但目前的方法并没有充分考虑到每个患者瓣膜解剖结构的独特性、存在允许外部纤维层(纤维层和心室层)剪切的中间海绵状垫以及需要自体瓣膜间质细胞。在这项研究中,我们提出了一种基于生物反应器培养骨髓间充质干细胞接种的、由分层胶原支架组装的瓣膜状结构的心脏瓣膜组织工程新方法。纤维支架通过脱细胞猪心包和脱细胞及弹性蛋白酶处理猪肺动脉制备,海绵状支架制备。为了创建解剖学上正确的构建体,我们使用天然猪主动脉瓣创建硅模具,将两个相同的纤维支架干燥到模具上,并使用五倍半乳糖基葡萄糖稳定它们,五倍半乳糖基葡萄糖是一种可逆结合胶原蛋白的多酚,可减少生物降解。层与蛋白质/醛基支架生物粘合剂融合并中和以降低细胞毒性。在瓣膜状分层支架内插入接种有人骨髓源性干细胞的海绵状支架,并在原始主动脉根部内缝合。最终产品安装在心脏瓣膜生物反应器中,并在细胞培养条件下循环。8 天后,大多数细胞仍存活,显著伸长,并对波形蛋白呈阳性染色,类似于天然人瓣膜间质细胞,表明我们的方法具有可行性。