Department of Orthopaedic Surgery, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325015, China.
Zhejiang Engineering Research Center for Tissue Repair Materials, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang, 325000, China.
Small. 2024 Jun;20(26):e2309868. doi: 10.1002/smll.202309868. Epub 2024 Jan 23.
Critical-sized segmental long bone defects represent a challenging clinical dilemma in the management of battlefield and trauma-related injuries. The residual bone marrow cavity of damaged long bones contains many bone marrow mesenchymal stem cells (BMSCs), which provide a substantial source of cells for bone repair. Thus, a three-dimensional (3D) vertically aligned nanofiber scaffold (VAS) is developed with long channels and large pore size. The pore of VAS toward the bone marrow cavity after transplantation, enables the scaffolds to recruit BMSCs from the bone marrow cavity to the defect area. In vivo, it is found that VAS can significantly shorten gap distance and promote new bone formation compared to the control and collagen groups after 4 and 8 weeks of implantation. The single-cell sequencing results discovered that the 3D nanotopography of VAS can promote BMSCs differentiation to chondrocytes and osteoblasts, and up-regulate related gene expression, resulting in enhancing the activities of bone regeneration, endochondral ossification, bone trabecula formation, bone mineralization, maturation, and remodeling. The Alcian blue and bone morphogenetic protein 2 (BMP-2) immunohistochemical staining verified significant cartilage formation and bone formation in the VAS group, corresponding to the single-cell sequencing results. The study can inspire the design of next-generation scaffolds for effective long-bone regeneration is expected by the authors.
临界尺寸节段性长骨缺损是战场和创伤相关损伤治疗中具有挑战性的临床难题。受损长骨的残余骨髓腔包含许多骨髓间充质干细胞(BMSCs),为骨修复提供了大量细胞来源。因此,开发了一种具有长通道和大孔径的三维(3D)垂直排列纳米纤维支架(VAS)。移植后,VAS 朝向骨髓腔的孔使支架能够将 BMSCs 从骨髓腔招募到缺损区域。在体内,与对照组和胶原组相比,植入 4 周和 8 周后,VAS 可显著缩短间隙距离并促进新骨形成。单细胞测序结果发现,VAS 的 3D 纳米形貌可促进 BMSCs 向软骨细胞和成骨细胞分化,并上调相关基因表达,从而增强骨再生、软骨内化骨、骨小梁形成、骨矿化、成熟和重塑的活性。阿利新蓝和骨形态发生蛋白 2(BMP-2)免疫组织化学染色证实 VAS 组有明显的软骨形成和骨形成,与单细胞测序结果相对应。作者希望这项研究能激发下一代有效长骨再生支架的设计。