Weymann Alexander, Radovits Tamás, Schmack Bastian, Li Shiliang, Korkmaz Sevil, Soós Pál, Istók Roland, Veres Gabor, Chaimow Nicole, Karck Matthias, Szabó Gábor
Heart and Marfan Center, Department of Cardiac Surgery, University of Heidelberg, Heidelberg, Germany; Department of Cardiothoracic Transplantation and Mechanical Circulatory Support, Royal Brompton & Harefield NHS Foundation Trust, Harefield, Middlesex, UK.
Artif Organs. 2014 Jul;38(7):E118-28. doi: 10.1111/aor.12321. Epub 2014 May 20.
Tissue engineering of cardiovascular structures represents a novel approach to improve clinical strategies in heart valve disease treatment. The aim of this study was to engineer decellularized atrioventricular heart valve neoscaffolds with an intact ultrastructure and to reseed them with umbilical cord-derived endothelial cells under physiological conditions in a bioreactor environment. Mitral (n=38) and tricuspid (n=36) valves were harvested from 40 hearts of German Landrace swine from a selected abattoir. Decellularization of atrioventricular heart valves was achieved by a detergent-based cell extraction protocol. Evaluation of the decellularization method was conducted with light microscopy and quantitative analysis of collagen and elastin content. The presence of residual DNA within the decellularized atrioventricular heart valves was determined with spectrophotometric quantification. The described decellularization regime produced full removal of native cells while maintaining the mechanical stability and the quantitative composition of the atrioventricular heart valve neoscaffolds. The surface of the xenogeneic matrix could be successfully reseeded with in vitro-expanded human umbilical cord-derived endothelial cells under physiological flow conditions. After complete decellularization with the detergent-based protocol described here, physiological reseeding of the xenogeneic neoscaffolds resulted in the formation of a confluent layer of human umbilical cord-derived endothelial cells. These results warrant further research toward the generation of atrioventricular heart valve neoscaffolds on the basis of decellularized xenogeneic tissue.
心血管结构的组织工程是一种改善心脏瓣膜疾病临床治疗策略的新方法。本研究的目的是构建具有完整超微结构的去细胞化房室心脏瓣膜新支架,并在生物反应器环境中的生理条件下用脐带来源的内皮细胞重新接种。从选定屠宰场的40头德国长白猪心脏中获取二尖瓣(n = 38)和三尖瓣(n = 36)。通过基于去污剂的细胞提取方案实现房室心脏瓣膜的去细胞化。采用光学显微镜以及对胶原蛋白和弹性蛋白含量的定量分析对去细胞化方法进行评估。用分光光度法定量测定去细胞化房室心脏瓣膜中残留DNA的存在情况。所描述的去细胞化方案在保持房室心脏瓣膜新支架的机械稳定性和定量组成的同时完全去除了天然细胞。在生理流动条件下,异种基质的表面可以成功地用体外扩增的人脐带来源的内皮细胞重新接种。用此处描述的基于去污剂的方案完全去细胞化后,异种新支架的生理重新接种导致形成了一层汇合的人脐带来源的内皮细胞。这些结果为基于去细胞化异种组织生成房室心脏瓣膜新支架的进一步研究提供了依据。