3D-printed triboelectric scaffolds for fabricating BMSC-derived cartilage to repair bone defects and promote endochondral ossification

软骨内骨化 软骨 化学 生物医学工程 骨化 脚手架 再生(生物学) 间充质干细胞 骨愈合 膜内骨化 细胞生物学 解剖 组织工程 软骨发生 骨细胞 材料科学 体内 干细胞 破骨细胞 软骨细胞 祖细胞 刺激 骨组织
作者
Yuanqi Ma,Xingqi Song,Bin Luo,Baoshuai Bai,Chen Jin,Shanhong Xie,Meilin Huang,Jie Luo,Zhengwei You,Dong Lei,Guangdong Zhou
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:58: 685-700 被引量:3
标识
DOI:10.1016/j.bioactmat.2025.11.044
摘要

The harsh microenvironment characterized by avascularity and hypoxia presents a significant challenge for bone regeneration following refractory bone defects. Tissue engineering combined with electrotherapy has emerged as a promising alternative for repairing bone defects, offering advantages such as accelerated healing and the restoration of physiological functions in regenerated bone. In this study, we propose a strategy for constructing tissue-engineered cartilage derived from bone marrow stem cells (BMSCs) for bone regeneration, utilizing 3D-printed triboelectric scaffolds (TES). The TES scaffold is fabricated from biodegradable bioelastomer and conductive biomaterial, featuring excellent biomimetic elasticity and hydrophobicity. The TES contains numerous hydrophobic microporous units, enabling in situ self-powered stimulation in vivo. The conductivity of the TES has been shown to enhance the chondrogenic differentiation potential of BMSCs during in vitro induction into tissue-engineered cartilage. Notably, the TES scaffold was more effective in promoting endochondral ossification of tissue-engineered cartilage in vivo. The in vivo osteogenesis mechanism of the TES group was further analyzed through proteomics, revealing that TES facilitated actin cytoskeleton remodeling, activated the PI3K-Akt pathway, provided metabolic support, and enhanced intercellular communication to drive the endochondral ossification process. Finally, in situ skull defect repair in rabbits successfully demonstrated the efficacy of TES electrical stimulation in promoting tissue-engineered endochondral ossification, thereby achieving bone defect regeneration and providing an effective biological strategy for the repair of refractory bone defects.
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