间充质干细胞
生物医学工程
骨形态发生蛋白2
骨愈合
微球
再生(生物学)
骨髓
材料科学
骨形态发生蛋白
细胞生物学
化学
体外
免疫学
医学
解剖
生物
生物化学
化学工程
工程类
基因
作者
W.H. Chang,Peipei Lu,Shuxiang Li,Jie Xiang,Jiachen Liu,Yimin Wang,Lei Zhang,Han Sun
标识
DOI:10.1021/acsbiomaterials.4c01720
摘要
Currently, bone defects remain a major challenge in clinical treatment. Recruiting target cells at the defect site and inducing them to differentiate into bone tissue are effective treatment methods. In previous studies, we used the CD271 antibody to construct bone marrow mesenchymal stem cell (BMSC) recruitment microspheres for the treatment of bone defects. However, the osteoconductivity of the microspheres themselves was poor, and the system lacked osteoinductivity, which affected the repair efficiency. In this study, we prepared submillimeter-sized porous chitosan (CS) microspheres through process optimization, and the BMSCs were able to directly adhere and proliferate on their surfaces. After the bioconjugation of the CD271 antibody, bone morphogenetic protein-2 (BMP-2) was further loaded onto the pore structure of microspheres to obtain the injectable microspheres with BMSC recruitment and osteogenic differentiation induction functions. Microspheres could efficiently recruit BMSCs through the combined action of the CD271 antibody and BMP-2 and further induce the recruited BMSCs, differentiating into osteoblasts through BMP-2, which ultimately exhibited promising bone regeneration ability in rats. We expect that the novel functional microspheres have great potential in biomedical applications for in situ treatment of bone defects.
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