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Angiogenic properties of dental pulp stem cells conditioned medium on endothelial cells in vitro and in rodent orthotopic dental pulp regeneration

机译:牙髓牙髓干细胞条件培养基在体外和啮齿动物原位牙髓再生中的血管生成特性

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摘要

Objectives: To evaluate the effect of SHED-CM on the proliferation, differentiation, migration ability, cell death, gene expression and production of VEGF of HUVEC in vitro and in a rodent orthotopic dental pulp regeneration. Methods: Three culture media [M199, DMEM/Ham's F12 and DMEM/Ham's F12 conditioned by SHEDs] were used as experimental groups. SHED-CM was prepared maintaining confluent cells in culture without serum for 3 days. The proliferation and cell death marker of HUVECs were assessed using flow cytometry. The capacity of formation of vascular-like structures was analyzed in cells grown over Matrigel® in hypoxic condition. HUVECs migration was followed using the scratch test. VEGF-A expression in HUVECs was assessed using real time RT-qPCR; and VEGF synthesis with ELISA test. SHED-CM was also applied in rodent ortotopic model of dental pulp regeneration in rats. The formed tissue was submitted to histological and immunohistochemical analyses. Results: SHED-CM promoted significantly lower expression of 7AAD in HUVECs; whereas the expression of the Ki67 was similar in all groups. The vascular-like structures were observed in all groups. Migration of SHED-CM group was faster than DMEM/Ham's F12. SHED-CM induced similar expression of VEGF-A than M199, and higher than DMEM/Ham's F12. SHED-CM induced significantly higher VEGF synthesis than other media. SHED-CM induced formation of a vascularized connective tissue inside the root canal. Conclusion: The study showed that SHEDs release angiogenic and cytoprotective factors, which are of great importance for tissue engineering. Clinical significance: SHED-CM could be an option to the use of stem cells in tissue engineering.
机译:目的:评估血小曲线对Huvec在体外和啮齿动物原位牙髓再生的增殖,分化,迁移能力,细胞死亡,细胞死亡,基因表达和生产的影响。方法:三种培养介质[M199,DMEM / HAM的F12和DMEM / HAM的F12用SHEDS]用作实验组。在没有血清的情况下,在没有血清的培养物中制备杂交细胞3天。使用流式细胞术评估HUVEC的增殖和细胞死亡标记。在缺氧条件下在Matrigel®种植的细胞中分析了血管状结构的形成能力。使用临时测试,遵循Huvecs迁移。使用实时RT-QPCR评估Huvecs中的VEGF-A表达;和VEGF合成用ELISA测试。 Shed-cm也应用于大鼠牙髓再生的啮齿动物Orotopic模型。将形成的组织提交给组织学和免疫组织化学分析。结果:Shed-CM在Huvecs中促进了7AAD的显着降低;虽然KI67的表达在所有群体中相似。在所有组中观察到血管状结构。 SHED-CM组的迁移比DMEM / HAM的F12更快。 Shed-cm诱导类似VEGF-a比m199的表达,高于DMEM / HAM的F12。 Shed-cm诱导比其他介质的VEGF合成显着更高。 Shed-cm诱导从根管内形成血管化结缔组织。结论:该研究表明,脱落释放血管生成和细胞保护因子,这对组织工程具有重要意义。临床意义:Shed-cm可以是在组织工程中使用干细胞的选择。

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