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首页> 外文期刊>Journal of biomaterials and tissue engineering >In Vitro Induction of Epithelialization of Human Gingival Fibroblasts by Mesenchymal Stem Cells Conditioned Medium (MSCCM) and Its Effects on the Secretion of Interleukin-6 and Interleukin-1beta
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In Vitro Induction of Epithelialization of Human Gingival Fibroblasts by Mesenchymal Stem Cells Conditioned Medium (MSCCM) and Its Effects on the Secretion of Interleukin-6 and Interleukin-1beta

机译:间充质干细胞条件培养基(MSCCM)对人牙龈成纤维细胞上皮细胞的体外诱导及其对白细胞介素-6和白细胞介素-1β分泌的影响

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摘要

Epithelial injury is difficult to restore normal structure and function upon self-repair. Tissue engineering technology provides hope for epithelial injury. It is showed that human gingival fibroblasts (HGFs) could be ideal seed cells for tissue repair. Our study intends to assess mesenchymal stem cell (MSC) conditioned mediums effect on HGFs epithelization. HGFs were cultured In Vitro and divided into two groups, including control maintained at complete DMEM medium containing 10% FBS and induction group treated by MSC conditioned medium followed by analysis of cell proliferation by MTT assay, cell apoptosis, Keratin and vimentin expressions by real-time PCR and Western blot. IL-6 and IL-1 beta secretions by ELISA. MSC conditioned medium induction significantly inhibited HGFs proliferation, increased keratin mRNA and protein levels, reduced vimentin expression, and enhanced IL-6 and IL-1 beta secretions compared with control (P < 0.05). Caspase 3 activity failed to exhibit statistical significance (P > 0.05). MSC conditioned medium induced HGFs epithelization and promoted IL-6 and IL-1 beta secretions, thus providing theoretical basis for the repair function of HGFs.
机译:上皮损伤难以恢复正常结构并在自修复时发挥作用。组织工程技术为上皮损伤提供了希望。结果表明,人牙龈成纤维细胞(HGFS)可以是用于组织修复的理想种子细胞。我们的研究旨在评估间充质干细胞(MSC)条件培养基对HGFS上皮化的影响。 HGFS在体外培养并分为两组,包括在含有10%FBS和MSC条件培养基处理的诱导组的完全DMEM培养基中保持的对照,然后通过MTT测定分析细胞增殖,细胞凋亡,角蛋白和Vimentin表达式时间PCR和Western印迹。 ELISA的IL-6和IL-1β分泌物。 MSC条件培养基诱导显着抑制HGFS增殖,增加角蛋白mRNA和蛋白质水平,降低的Vimentin表达和增强的IL-6和IL-1β分泌物(P <0.05)。 Caspase 3活性未能表现出统计学意义(P> 0.05)。 MSC条件培养基诱导HGFS上皮化和促进IL-6和IL-1β分泌物,从而为HGF的修复功能提供了理论依据。

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