明胶甲基丙烯酰胺水凝胶负载骨髓间充质干细胞来源外泌体修复大鼠颅骨骨缺损的研究

    Effects of gelatin methacryloyl hydrogel loaded with bone marrow mesenchymal stem cells-derived exosomes in the repair of rat calvarial defect

    • 摘要:
      目的 评估明胶甲基丙烯酰(GelMA)水凝胶联合骨髓间充质干细胞(BMSC)来源外泌体(EXO)对大鼠颅骨缺损修复的协同作用。
      方法 制备GelMA水凝胶,并利用电镜观察微观结构,电子万能试验机计算水凝胶样本的压缩强度。提取BMSC来源外泌体。Western blotting和电镜进行验证。活/死细胞染色实验GelMA对BMSC的存活率影响。颅骨缺损模型,分为NC组、GelMA组和GelMA+EXO组,每组3只,观察8周,Micro-CT、三维重建和HE染色证实各组骨缺损情况。
      结果 GelMA具有优异的力学性能,可承受148 kPa压强及92%形变率。从BMSC上清液中提取的EXO经透射电镜观察呈典型杯状形态,纳米颗粒追踪分析显示其平均粒径为140 nm。Western blotting检测确认外泌体标志物CD63、CD81和CD9高表达(P<0.01),而Calnexin阴性。BMSC与GelMA共培养5 d后,活/死染色表明细胞存活率上升(P<0.01)。Micro-CT、三维重建和HE结果显示,相较于NC组,GelMA+EXO组新生骨最多(P<0.01)。
      结论 GelMA水凝胶联合BMSC来源EXO对大鼠颅骨缺损修复的具有协同作用。

       

      Abstract:
      Objective To evaluate the synergistic effects of gelatin methacryloyl (GelMA) hydrogel combined with bone marrow mesenchymal stem cells (BMSC)-derived exosomes (EXO) on the repair of rat calvarial defect.
      Methods GelMA hydrogel was prepared, and its microstructure was observed by electron microscopy, and the compressive strength of the hydrogel samples was calculated by an electronic universal testing machine. BMSC-derived exosomes were extracted. Western blotting and electron microscopy were used for verification. Live/dead cell staining was used to examine the effects of GelMA on the survival rate of BMSCs. The calvarial defect models were divided into the NC group, GelMA group and GelMA+EXO group, with 3 animals in each group and observation for 8 weeks. Micro-CT, three-dimensional reconstruction and HE staining were used to confirm the bone defect conditions in each group.
      Results GelMA had excellent mechanical properties, capable of withstanding a pressure of 148 kPa and deformation rate of 92%. The EXO extracted from the supernatant of BMSC were observed by transmission electron microscopy to present a typical cup-shaped morphology. Nanoparticle tracking analysis showed that its average particle size was 140 nm. Western blotting detection confirmed the high expression of exosome markers CD63, CD81 and CD9 (P < 0.01), while Calnexin was negative. After co-culture BMSC with GelMA for 5 days, live/dead staining indicated an increase in cell survival rate (P < 0.01). The results of Micro-CT, three-dimensional reconstruction and HE showed that compared with the NC group, the GelMA+EXO group had the most new bones (P < 0.01).
      Conclusions GelMA hydrogel combined with BMSC-derived EXO has a synergistic effect on the repair of rat calvarial defect.

       

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