Trinity Centre for Bioengineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.
Exp Eye Res. 2013 Mar;108:42-7. doi: 10.1016/j.exer.2012.12.012. Epub 2012 Dec 31.
The main obstacle to successfully engineering corneal tissue has been the replication of the structural and biochemical composition of native cornea in a scaffold. In recent years decellularized corneas have been under investigation as an alternative scaffold source for use in engineering cornea. Several strategies for lysing cells and removing cellular material from corneas are discussed. The removal of such cellular components and antigen molecules whilst maintaining the corneal extracellular matrix components and architecture is required to generate scaffolds capable of generating functional tissue grafts suitable for transplantation. Different techniques to ascertain the degree of decellularization and the change in structural, mechanical and biological characteristics of the corneas after treatment are examined. In addition several in vitro and in vivo studies have been performed to ascertain the suitability of decellularized corneas as a scaffold for restoring vision.
成功构建角膜组织的主要障碍一直是在支架中复制天然角膜的结构和生化组成。近年来,脱细胞角膜作为一种替代支架来源,用于工程角膜,受到了广泛的研究。本文讨论了几种裂解细胞和从角膜中去除细胞物质的策略。需要去除这些细胞成分和抗原分子,同时保留角膜细胞外基质成分和结构,才能生成能够生成适合移植的功能性组织移植物的支架。还检查了不同的技术来确定脱细胞化的程度,以及处理后角膜的结构、机械和生物学特性的变化。此外,还进行了一些体外和体内研究,以确定脱细胞角膜作为恢复视力的支架的适用性。