The effect of induced membranes combined with enhanced bone marrow and 3D PLA‐HA on repairing long bone defects in vivo

聚乳酸 髂嵴 体内 脚手架 骨愈合 间充质干细胞 生物医学工程 骨髓 生物相容性 再生(生物学) 3d打印 阻隔膜 骨髓抽出物 化学 材料科学 解剖 病理 细胞生物学 医学 生物 生物化学 有机化学 聚合物 生物技术
作者
Zhiqing Liu,Yu‐Wei Ge,Linyuan Zhang,Yueting Wang,Cheng Guo,Kai Feng,Shengbing Yang,Zanjing Zhai,Yingjun Chi,Jie Zhao,Fengxiang Liu
出处
期刊:Journal of Tissue Engineering and Regenerative Medicine [Wiley]
卷期号:14 (10): 1403-1414 被引量:26
标识
DOI:10.1002/term.3106
摘要

The repair of large bone defects has always been a challenge, especially with respect to regeneration capacity and autogenous bone availability. To address this problem, we fabricated a 3D-printed polylactic acid (PLA) and hydroxyapatite (HA) scaffold (3D-printed PLA-HA, providing scaffold) loaded with enhanced bone marrow (eBM, providing seed cells) combined with induced membrane (IM, providing grow factors) to repair large radial defects in rabbits. in vitro assays, we demonstrated that 3D-printed PLA-HA had excellent biocompatibility, as shown by co-culturing with mesenchymal stem cells (MSCs); eBM-derived MSCs exhibited considerable differentiation potential, as shown in trilineage differentiation assays. To investigate bone formation efficacy in vivo, the rabbit radial long bone defect model was established. In the first stage, polymethylmethacrylate (PMMA) was inserted into the bone defect to stimulate the formation of IM; in the second stage, iliac crest bone graft (ICBG) with IM, PLA-HA alone with the removal of IM, PLA-HA with IM, and PLA-HA in conjunction with IM and eBM were sequentially applied to repair the long bone defect. At 8, 12, and 16 weeks, X-ray plain radiography, microcomputed tomography, and histological analysis were performed to evaluate the efficacy of bone repair and bone regeneration in each group. We found that IM combined with PLA-HA and eBM prominently enhanced bone repair and reconstruction, equivalent to that of IM/ICBG. Taken together, the data suggest that PLA-HA loaded with eBM combined with IM can be an alternative to IM with bone autografts for the treatment of large bone defects.
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