Engineered periosteum-diaphysis substitutes with biomimetic structure and composition promote the repair of large segmental bone defects

Yu, Lili and Wei, Qiang and Li, Jiaying and Wang, Huan and Meng, Qingchen and Xie, En and Li, Zexi and Li, Kexin and Shu, Wenmiao Will and Wu, Junxi and Yang, Lei and Cai, Yan and Han, Fengxuan and Li, Bin (2023) Engineered periosteum-diaphysis substitutes with biomimetic structure and composition promote the repair of large segmental bone defects. Composites Part B: Engineering, 252. 110505. ISSN 1359-8368 (https://doi.org/10.1016/j.compositesb.2023.110505)

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Abstract

The repair of large segmental bone defects remains a big challenge due to limited self-healing capacity of bone. Digging into the structure and composition of natural long bone let us realize that the periosteum cambium on the surface of diaphysis plays a crucial role in bone repair. In this study, we explored the feasibility of using a tissue-engineered periosteum-diaphysis substitute to repair the large segmental bone defects. To create an artificial periosteum cambium, bone marrow mesenchymal stem cells (BMSCs) and endothelial progenitor cells (EPCs) were co-cultured on electrospun silk fibroin (SF) fibrous membranes for mimicking the cellular composition and microstructure of cambium layer of the native periosteum. These SF membranes supported the adhesion and proliferation of both BMSCs and EPCs. In addition, we found that a 1:1 ratio of BMSCs and EPCs supported osteogenesis and angiogenesis optimally. This biomimetic periosteum layer was integrated with artificial diaphysis made of tubular SF scaffolds to construct a biomimetic periosteum-diaphysis substitute. Animal studies confirmed that the biomimetic periosteum-diaphysis substitutes promoted the repair of critical-size bone defects of rabbit radius. Furthermore, the transplanted biomimetic periosteum-diaphysis substitute could prevent the growth of fibrous tissues in the bone defect, and thus reduce the occurrence of nonunion. This study described a promising tissue engineering strategy for the repair of large segmental bone defects.

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