Weber Miriam, Gonzalez de Torre Israel, Moreira Ricardo, Frese Julia, Oedekoven Caroline, Alonso Matilde, Rodriguez Cabello Carlos J, Jockenhoevel Stefan, Mela Petra
1 Department of Tissue Engineering and Textile Implants, Institute of Applied Medical Engineering, Helmholtz Institute, RWTH Aachen University , Aachen, Germany .
2 G.I.R. Bioforge, University of Valladolid , CIBER-BBN, Valladolid, Spain .
Tissue Eng Part C Methods. 2015 Aug;21(8):832-40. doi: 10.1089/ten.TEC.2014.0396. Epub 2015 Mar 31.
Heart valves are elaborate and highly heterogeneous structures of the circulatory system. Despite the well accepted relationship between the structural and mechanical anisotropy and the optimal function of the valves, most approaches to create tissue-engineered heart valves (TEHVs) do not try to mimic this complexity and rely on one homogenous combination of cells and materials for the whole construct. The aim of this study was to establish an easy and versatile method to introduce spatial diversity into a heart valve fibrin scaffold. We developed a multiple-step injection molding process that enables the fabrication of TEHVs with heterogeneous composition (cell/scaffold material) of wall and leaflets without the need of gluing or suturing components together, with the leaflets firmly connected to the wall. The integrity of the valves and their functionality was proved by either opening/closing cycles in a bioreactor (proof of principle without cells) or with continuous stimulation over 2 weeks. We demonstrated the potential of the method by the two-step molding of the wall and the leaflets containing different cell lines. Immunohistology after stimulation confirmed tissue formation and demonstrated the localization of the different cell types. Furthermore, we showed the proof of principle fabrication of valves using different materials for wall (fibrin) and leaflets (hybrid gel of fibrin/elastin-like recombinamer) and with layered leaflets. The method is easy to implement, does not require special facilities, and can be reproduced in any tissue-engineering lab. While it has been demonstrated here with fibrin, it can easily be extended to other hydrogels.
心脏瓣膜是循环系统中精巧且高度异质的结构。尽管结构和机械各向异性与瓣膜的最佳功能之间的关系已被广泛认可,但大多数制造组织工程心脏瓣膜(TEHV)的方法并未尝试模拟这种复杂性,而是依赖于细胞和材料的单一均匀组合来构建整个瓣膜。本研究的目的是建立一种简便且通用的方法,将空间多样性引入心脏瓣膜纤维蛋白支架中。我们开发了一种多步注射成型工艺,能够制造出壁和瓣叶具有异质组成(细胞/支架材料)的TEHV,无需将组件胶合或缝合在一起,瓣叶与壁牢固连接。通过在生物反应器中进行开闭循环(无细胞的原理验证)或持续刺激两周,证明了瓣膜的完整性及其功能。我们通过对包含不同细胞系的壁和瓣叶进行两步成型,展示了该方法的潜力。刺激后的免疫组织学证实了组织形成,并显示了不同细胞类型的定位。此外,我们展示了使用不同材料制造瓣膜的原理验证,壁使用纤维蛋白,瓣叶使用纤维蛋白/类弹性蛋白重组体的混合凝胶,并具有分层的瓣叶。该方法易于实施,不需要特殊设备,并且可以在任何组织工程实验室中重复。虽然这里以纤维蛋白为例进行了展示,但它可以很容易地扩展到其他水凝胶。