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明胶-甲基丙烯酰复合载体的研制及其在骨形态发生蛋白-2 传递中的应用:一种潜在的脊柱融合策略。

Development of gelatin-methacryloyl composite carriers for bone morphogenetic Protein-2 delivery: A potential strategy for spinal fusion.

机构信息

Department of Spine Surgery, Honghui Hospital, Xi'an Jiaotong University, Shaanxi, PR China.

Department of Orthopedics, Lanzhou University Second Hospital, Lanzhou, PR China.

出版信息

J Biomater Appl. 2024 Sep;39(3):195-206. doi: 10.1177/08853282241258302. Epub 2024 Jun 15.

Abstract

To reduce the risk of nonunion after spinal fusion surgery, the in situ transplantation of bone marrow mesenchymal stem cells (BMSCs) induced toward osteogenic differentiation by bone morphogenetic protein-2 (BMP2) has been proven effective. However, the current biological agents used for transplantation have limitations, such as a short half-life and low bioavailability. To address this, our study utilized a safe and effective gelatin-methacryloyl (GelMA) as a carrier for BMP2. In vitro, experiments were conducted to observe the ability of this composite vehicle to induce osteogenic differentiation of BMSCs. The results showed that the GelMA hydrogel, with its critical properties and controlled release performance of BMP2, exhibited a slow release of BMP2 over 30 days. Moreover, the GelMA hydrogel not only enhanced the proliferation activity of BMSCs but also significantly promoted their osteogenic differentiation ability, surpassing the BMP2 effects. To investigate the potential of the GelMA-BMP2 composite vehicle, a rabbit model was employed to explore its ability to induce in situ intervertebral fusion by BMSCs. Transplantation experiments in rabbits demonstrated the effective induction of intervertebral bone fusion by the GelMA-BMP2-BMSC composite vehicle. In conclusion, the GelMA-BMP2-BMSC composite vehicle shows promising prospects in preclinical translational therapy for spinal intervertebral fusion. It addresses the limitations of current biological agents and offers a controlled release of BMP2, enhancing the proliferation and osteogenic differentiation of BMSCs.

摘要

为降低脊柱融合术后骨不连的风险,经骨形态发生蛋白 2(BMP2)诱导向成骨分化的骨髓间充质干细胞(BMSCs)原位移植已被证明是有效的。然而,目前用于移植的生物制剂存在半衰期短、生物利用度低等局限性。针对这一问题,本研究利用安全有效的明胶甲基丙烯酰(GelMA)作为 BMP2 的载体。在体外,进行了实验以观察该复合载体诱导 BMSCs 成骨分化的能力。结果表明,GelMA 水凝胶具有关键性能和 BMP2 的控制释放性能,可在 30 天内缓慢释放 BMP2。此外,GelMA 水凝胶不仅增强了 BMSCs 的增殖活性,而且还显著促进了其成骨分化能力,超过了 BMP2 的作用。为了研究 GelMA-BMP2 复合载体的潜力,采用兔模型来探讨其通过 BMSCs 诱导原位椎间融合的能力。兔体内移植实验表明,GelMA-BMP2-BMSC 复合载体可有效诱导椎间骨融合。总之,GelMA-BMP2-BMSC 复合载体在脊柱椎间融合的临床前转化治疗中具有广阔的前景。它解决了当前生物制剂的局限性,并提供了 BMP2 的控制释放,增强了 BMSCs 的增殖和成骨分化能力。

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