Aging-Induced Discrepant Response of Fracture Healing is Initiated from the Organization and Mineralization of Collagen Fibrils in Callus.

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Biomaterials Science & Engineering Pub Date : 2025-01-20 DOI:10.1021/acsbiomaterials.4c01490
Fa Liu, Yiwei Hu, Yuzhi Zhang, Chenxi Ren, Feng Qiao, Hui Yang, Huiyun Xu, Pengfei Yang
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Abstract

Fracture healing is a complex process during which the bone restores its structural and mechanical integrity. Collagen networks and minerals are the fundamental components to rebuild the bone matrix in callus. It has been recognized that bone quality could be impaired during aging. However, how the structural and mechanical recovery of fracture healing is influenced by aging, particularly from the perspective of organization and mineralization of the collagen network in callus, remains unclear. A tibial fracture model was established for both the young (5 weeks) and aged mice (68 weeks). On the 21st day postfracture, the characteristics of the collagen network, mineralization, and the nanoscale mechanical properties of the callus were assessed. The results indicated that aging postpones the fracture healing process, leading to incomplete microstructure, less mineral content and mineralization, and weaker mechanical properties of callus. In the aged mice, the internal fixation and mechanical immobilization promoted the mineralization of callus by increasing mineral crystal length and mineral-to-matrix ratio by 48 and 42% compared to the internal fixation and free movement control group, respectively. By contrast, in the young mice, the internal fixation and mechanical immobilization induced disordered collagen fibrils and decreased the crystal length and mineral-to-matrix ratio by 32 and 36%, compared to the internal fixation and free movement control group, respectively. The present findings suggested that the aging-induced structure and mechanical differences of callus during fracture healing initiate from the organization and mineralization of collagen fibrils. Multiscale structural and mechanical analysis suggested mechanical immobilization is beneficial to the structure, composition, and mechanics of callus in the aged mice while impairing the organization and mineralization of collagen fibril in the callus of the young mice. These findings suggested that different mechanical intervention strategies should be adopted for fracture healing at different ages, which provides valuable insights for the clinical treatment of bone fracture.

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衰老诱导的骨折愈合差异反应是由骨痂中胶原原纤维的组织和矿化引发的。
骨折愈合是一个复杂的过程,在此过程中,骨恢复其结构和机械完整性。胶原蛋白网络和矿物质是骨痂中重建骨基质的基本成分。人们已经认识到,随着年龄的增长,骨质量可能会受到损害。然而,骨折愈合的结构和机械恢复如何受到老化的影响,特别是从愈伤组织中胶原网络的组织和矿化的角度来看,尚不清楚。分别建立幼龄(5周龄)和老年(68周龄)小鼠胫骨骨折模型。骨折后第21天,观察骨痂的胶原网络、矿化特征及纳米尺度力学性能。结果表明,时效延缓了骨折愈合过程,导致愈伤组织微观结构不完整,矿物含量和矿化减少,力学性能变弱。在老龄小鼠中,与内固定组和自由运动对照组相比,内固定组和机械固定组分别增加了48%和42%的矿物晶体长度和矿物基质比,促进了愈伤组织的矿化。相比之下,在幼龄小鼠中,与内固定和自由运动对照组相比,内固定和机械固定诱导胶原原纤维紊乱,晶体长度和矿物-基质比分别减少32%和36%。研究结果表明,骨折愈合过程中愈伤组织的结构和力学差异源于胶原原纤维的组织和矿化。多尺度结构和力学分析表明,机械固定有利于老年小鼠愈伤组织的结构、组成和力学,但会损害年轻小鼠愈伤组织中胶原纤维的组织和矿化。提示不同年龄骨折愈合应采用不同的机械干预策略,为骨折的临床治疗提供有价值的见解。
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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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