Department of Biohybrid and Medical Textiles (BioTex), AME - Institute of Applied Medical Engineering, Helmholtz Institute of RWTH Aachen University & Hospital, 52074 Aachen, Germany.
Electron Microscopy Facility, Institute of Pathology, RWTH Aachen University Hospital, 52074 Aachen, Germany.
Int J Mol Sci. 2020 Jun 13;21(12):4226. doi: 10.3390/ijms21124226.
Rapid vascularization is required for the regeneration of dental pulp due to the spatially restricted tooth environment. Extracellular vesicles (EVs) released from mesenchymal stromal cells show potent proangiogenic effects. Since EVs suffer from rapid clearance and low accumulation in target tissues, an injectable delivery system capable of maintaining a therapeutic dose of EVs over a longer period would be desirable. We fabricated an EV-fibrin gel composite as an in situ forming delivery system. EVs were isolated from dental pulp stem cells (DPSCs). Their effects on cell proliferation and migration were monitored in monolayers and hydrogels. Thereafter, endothelial cells and DPSCs were co-cultured in EV-fibrin gels and angiogenesis as well as collagen deposition were analyzed by two-photon laser microscopy. Our results showed that EVs enhanced cell growth and migration in 2D and 3D cultures. EV-fibrin gels facilitated vascular-like structure formation in less than seven days by increasing the release of VEGF. The EV-fibrin gel promoted the deposition of collagen I, III, and IV, and readily induced apoptosis during the initial stage of angiogenesis. In conclusion, we confirmed that EVs from DPSCs can promote angiogenesis in an injectable hydrogel in vitro, offering a novel and minimally invasive strategy for regenerative endodontic therapy.
由于牙齿所处的空间环境受限,牙髓再生需要快速的血管化。间充质基质细胞释放的细胞外囊泡(EVs)具有很强的促血管生成作用。由于 EVs 在体内易被快速清除且在靶组织中积累效率低,因此需要开发一种可注射的、能够在较长时间内维持治疗剂量 EVs 的递送系统。我们构建了一种 EV-纤维蛋白凝胶复合物作为原位形成的递送系统。从牙髓干细胞(DPSCs)中分离出 EVs。在单层和水凝胶中监测它们对细胞增殖和迁移的影响。然后,将内皮细胞和 DPSCs 共培养在 EV-纤维蛋白凝胶中,通过双光子激光显微镜分析血管生成和胶原蛋白沉积情况。结果表明,EVs 增强了 2D 和 3D 培养中的细胞生长和迁移。EV-纤维蛋白凝胶通过增加 VEGF 的释放,在不到 7 天的时间内促进了类似血管的结构形成。该凝胶还促进了胶原蛋白 I、III 和 IV 的沉积,并在血管生成的初始阶段诱导了细胞凋亡。总之,我们证实了 DPSCs 的 EVs 可以在体外的可注射水凝胶中促进血管生成,为再生性牙髓治疗提供了一种新颖的微创策略。