A Novel Strategy to Enhance the Bone Healing Efficacy of Composite Scaffolds via Induction of Cell Recruitment and Vascularization.

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2025-04-10 eCollection Date: 2025-01-01 DOI:10.34133/bmr.0185
Jeong In Kim, Thi Thu Trang Kieu, Jeong-Chae Lee
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Abstract

This study devised a novel strategy to develop a functionally improved scaffold that enhances the healing of large bone defects via synergistic activation of vascularization and cell recruitment. To this end, we fabricated round and ring-shaped silk fibroin/Broussonetia kazinoki (SFBK) composite scaffolds. The round scaffolds had a diameter of 1.5 mm, and the ring-shaped scaffolds had a 6-mm diameter with a 1.5-mm hole in the center. All scaffolds had a 3-mm thickness. A portion of round SFBKs was cross-linked with stromal cell-derived factor 1 (SDF-1), and ring-shaped scaffolds underwent in vitro angiogenic stimulation, in vivo vascularization, or both. These scaffolds were assembled by fitting a round SFBK into the center of a vascularized SFBK scaffold before implantation into a rat model with critical-sized calvarial defects. Implantation with puzzle-fitted scaffolds promoted bone regeneration, and the scaffold that underwent both SDF-1 immobilization and vascularization processes showed the greatest efficacy in the healing of defects. The bone healing efficacy of puzzle-fitted scaffolds involved their ability to stimulate microvascular network formation, collagen synthesis, and stem cell recruitment at defects. B. kazinoki-released calcium ions also participated in synergistic bone regeneration. These results suggest that the strategy of fitting SDF-1-linked SFBK into a vascularized ring-SFBK scaffold is useful in recruiting multipotent stem cells via newly formed blood vessels toward the center of scaffolds. This induces balanced and uniform bone regeneration. Overall, this study highlights the needs of calcium release, neovascularization, and stem cell recruitment for synergistic enhancement of bone regeneration.

一种通过诱导细胞募集和血管形成来增强复合支架骨愈合效果的新策略。
本研究设计了一种新的策略来开发一种功能改进的支架,通过协同激活血管化和细胞募集来增强大骨缺损的愈合。为此,我们制备了圆形和环状丝素蛋白/布氏菌(SFBK)复合支架。圆形支架直径为1.5 mm,环形支架直径为6mm,中间有1.5 mm孔。支架厚度均为3mm。部分圆形SFBKs与基质细胞衍生因子1 (SDF-1)交联,环形支架经历体外血管生成刺激,体内血管形成,或两者兼而有之。在植入具有临界尺寸颅骨缺损的大鼠模型之前,通过将圆形SFBK植入血管化的SFBK支架的中心来组装这些支架。拼图支架的植入促进了骨再生,同时经历了SDF-1固定和血管化过程的支架在修复缺陷方面表现出最大的效果。拼图支架的骨愈合功效包括其刺激微血管网络形成、胶原合成和干细胞在缺陷处募集的能力。B. kazinoki释放的钙离子也参与了协同骨再生。这些结果表明,将sdf -1连接的SFBK安装到血管化的环-SFBK支架中的策略有助于通过新形成的血管向支架中心募集多能干细胞。这诱导平衡和均匀的骨再生。总的来说,这项研究强调了钙释放、新生血管和干细胞募集对骨再生协同增强的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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