Tortorici Martina, Petersen Ansgar, Duda Georg N, Checa Sara
Julius Wolff Institute, Berlin Institute of Health at Charité-Universitätsmedizin Berlin, Berlin, Germany.
Front Bioeng Biotechnol. 2022 Mar 10;10:846665. doi: 10.3389/fbioe.2022.846665. eCollection 2022.
Current clinical treatments of osteochondral defects in articulating joints are frequently not successful in restoring articular surfaces. Novel scaffold-based tissue engineering strategies may help to improve current treatment options and foster a true regeneration of articulating structures. A frequently desired property of scaffolds is their ability to degrade over time and allow a full restoration of tissue and function. However, it remains largely unknown how scaffold degradation influences the mechanical stability of the tissue in a defect region and, in turn, the regenerative process. Such differing goals-supporting regeneration by degrading its own structure-can hardly be analyzed for tissue engineered constructs in clinical trials and preclinical experiments. Using an analysis, we investigated the degradation-induced modifications in material and architectural properties of a scaffold with strut-like architecture over the healing course and their influence on the mechanics-dependent tissue formation in osteochondral defects. The repair outcome greatly varied depending on the degradation modality, i.e. surface erosion or bulk degradation with and without autocatalysis, and of the degradation speed, i.e. faster, equal or slower than the expected repair time. Bulk degradation with autocatalysis, independently of degradation speed, caused the mechanical failure of the scaffold prior to osteochondral defect repair and was thereby deemed inappropriate for further application. On the other hand, scaffolds with strut-like architecture degrading by both surface erosion and bulk degradation with slow degradation speed resulted in comparably good repair outcomes, thereby indicating such degradation modalities as favorable for the application in osteochondral defects.
目前,关节软骨下骨缺损的临床治疗在恢复关节表面方面常常并不成功。基于新型支架的组织工程策略可能有助于改善当前的治疗选择,并促进关节结构的真正再生。支架通常期望具备的一个特性是它们能够随着时间推移而降解,并使组织和功能完全恢复。然而,支架降解如何影响缺损区域组织的机械稳定性,进而影响再生过程,在很大程度上仍然未知。对于临床试验和临床前实验中的组织工程构建体而言,这种通过降解自身结构来支持再生的不同目标很难进行分析。通过分析,我们研究了具有支柱状结构的支架在愈合过程中材料和结构特性因降解而产生的变化,以及它们对软骨下骨缺损中依赖力学的组织形成的影响。修复结果因降解方式(即表面侵蚀或有自催化和无自催化的整体降解)以及降解速度(即快于、等于或慢于预期修复时间)的不同而有很大差异。有自催化的整体降解,无论降解速度如何,都会在软骨下骨缺损修复之前导致支架的机械失效,因此被认为不适用于进一步应用。另一方面,具有支柱状结构且通过表面侵蚀和降解速度较慢的整体降解方式降解的支架,产生了相对较好的修复结果,从而表明这些降解方式有利于应用于软骨下骨缺损。