注射用磷酸钙骨水泥与 BMSCs 包裹的微胶囊结合,用于骨组织再生。

Yafei Yuan, Jiangqi Hu, Lipei Shen, Lin He, Yixuan Zhu, Dan Meng, Qingsong Jiang
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引用次数: 0

摘要

注射用磷酸钙骨水泥(CPC)在微创修复不规则骨缺损方面具有显著优势。然而,CPC 的主要局限性,包括成骨性能不足和孔隙率不够大,需要进一步研究和解决。本研究利用海藻酸盐-壳聚糖-精氨酸(ACA)微胶囊将大鼠骨间充质干细胞(rBMSCs)包裹并输送到 CPC 浆料中,同时建立多孔 CPC 支架以支持细胞生长。我们的研究结果表明,ACA 细胞微胶囊能有效保护细胞,并促进细胞向 CPC 糊状物中的输送,从而提高细胞植入后的存活率。此外,我们还发现 ACA+CPC 提取物能刺激 rBMSCs 的成骨分化。此外,大鼠颅顶骨缺损模型的研究结果表明,含有外源 rBMSCs 的 ACA 微胶囊最初能改善骨缺损内 CPC 的原位成骨潜能,为骨生长提供多个部位。随着时间的推移,外源性细胞的成骨潜能会逐渐减弱,但微胶囊形成的孔隙会通过将内源性细胞招募到成骨部位而持续支持骨形成。总之,利用装载 ACA 的干细胞微胶囊可令人满意地促进成骨和 CPC 降解,使其成为骨缺损移植的一种前景广阔的支架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Injectable calcium phosphate cement integrated with BMSCs-encapsulated microcapsules for bone tissue regeneration.

Injectable calcium phosphate cement (CPC) offers significant benefits for the minimally invasive repair of irregular bone defects. However, the main limitations of CPC, including its deficiency in osteogenic properties and insufficient large porosity, require further investigation and resolution. In this study, alginate-chitosan-alginate (ACA) microcapsules were used to encapsulate and deliver rat bone mesenchymal stem cells (rBMSCs) into CPC paste, while a porous CPC scaffold was established to support cell growth. Our results demonstrated that the ACA cell microcapsules effectively protect the cells and facilitate their transport into the CPC paste, thereby enhancing cell viability post-implantation. Additionally, the ACA + CPC extracts were found to stimulate osteogenic differentiation of rBMSCs. Furthermore, results from a rat cranial parietal bone defect model showed that ACA microcapsules containing exogenous rBMSCs initially improved thein situosteogenic potential of CPC within bone defects, providing multiple sites for bone growth. Over time, the osteogenic potential of the exogenous cells diminishes, yet the pores created by the microcapsules persist in supporting ongoing bone formation by recruiting endogenous cells to the osteogenic sites. In conclusion, the utilization of ACA loaded stem cell microcapsules satisfactorily facilitate osteogenesis and degradation of CPC, making it a promising scaffold for bone defect transplantation.

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