Golman Mikhail, Abraham Adam C, Kurtaliaj Iden, Marshall Brittany P, Hu Yizhong Jenny, Schwartz Andrea G, Guo X Edward, Birman Victor, Thurner Philipp J, Genin Guy M, Thomopoulos Stavros
Department of Orthopedic Surgery, Columbia University, New York, NY 10032, USA.
Department of Biomedical Engineering, Columbia University, New York, NY 10027, USA.
Sci Adv. 2021 Nov 26;7(48):eabi5584. doi: 10.1126/sciadv.abi5584.
Architectured materials offer tailored mechanical properties but are limited in engineering applications due to challenges in maintaining toughness across their attachments. The enthesis connects tendon and bone, two vastly different architectured materials, and exhibits toughness across a wide range of loadings. Understanding the mechanisms by which this is achieved could inform the development of engineered attachments. Integrating experiments, simulations, and previously unexplored imaging that enabled simultaneous observation of mineralized and unmineralized tissues, we identified putative mechanisms of enthesis toughening in a mouse model and then manipulated these mechanisms via in vivo control of mineralization and architecture. Imaging uncovered a fibrous architecture within the enthesis that controls trade-offs between strength and toughness. In vivo models of pathology revealed architectural adaptations that optimize these trade-offs through cross-scale mechanisms including nanoscale protein denaturation, milliscale load-sharing, and macroscale energy absorption. Results suggest strategies for optimizing architecture for tough bimaterial attachments in medicine and engineering.
结构化材料具有定制的机械性能,但由于在其连接处保持韧性方面存在挑战,在工程应用中受到限制。肌腱-骨连接部位连接着肌腱和骨骼这两种截然不同的结构化材料,并在广泛的载荷下表现出韧性。了解实现这一特性的机制可以为工程化连接部位的开发提供参考。通过整合实验、模拟以及此前未被探索的成像技术(该技术能够同时观察矿化和非矿化组织),我们在小鼠模型中确定了肌腱-骨连接部位增韧的假定机制,然后通过体内矿化和结构控制来操纵这些机制。成像揭示了肌腱-骨连接部位内的纤维结构,该结构控制着强度和韧性之间的权衡。病理学的体内模型揭示了结构适应性变化,这些变化通过跨尺度机制(包括纳米级蛋白质变性、毫米级载荷分担和宏观级能量吸收)优化了这些权衡。研究结果为医学和工程领域中优化坚韧双材料连接部位的结构提供了策略。