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Induction of Osteogenic Differentiation of Mesenchymal Stem Cells by Bioceramic Root Repair Material

机译:生物陶瓷根修复材料诱导间充质干细胞成骨分化

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摘要

This study aimed to evaluate the osteogenic activity of Endosequence Root Repair Material (ERRM) putty using rat mesenchymal stem cells (MSCs). The extract of set ERRM and ProRoot-mineral trioxide aggregate (MTA) (control) was cocultured with rat MSCs and incubated for one, three, and seven days. The cell viability and proliferation were assessed. A quantitative real-time polymerase chain reaction for bone morphogenetic protein-2 (BMP-2), alkaline phosphatase, bone sialoprotein, and osteocalcin gene expression was performed. Both materials enhanced cell viability and proliferation, which increased over time. On day seven, the cells treated with either material exhibited significantly greater cell viability compared with control untreated cells. MSCs treated with either material showed deeper alkaline phosphatase staining after three days compared to control untreated cells. Treated MSCs also exhibited upregulation of the gene expression of bone morphogenetic protein-2, alkaline phosphatase, bone sialoprotein, and osteocalcin. Both ERRM and ProRoot-MTA enhance the osteogenic differentiation of MSCs.
机译:这项研究旨在评估使用大鼠间质干细胞(MSCs)的内序列根修复材料(ERRM)油灰的成骨活性。将设置好的ERRM和ProRoot-三氧化二矿骨料(MTA)的提取物(对照)与大鼠MSC共培养,并孵育一,三和七天。评估细胞活力和增殖。进行了骨形态发生蛋白2(BMP-2),碱性磷酸酶,骨唾液蛋白和骨钙素基因表达的定量实时聚合酶链反应。两种材料均增强了细胞活力和增殖,并随时间增加。在第七天,与对照未处理的细胞相比,用两种材料处理的细胞均表现出明显更高的细胞活力。与未处理的对照细胞相比,用两种材料处理的MSC在三天后显示出更深的碱性磷酸酶染色。处理过的MSC也显示出骨形态发生蛋白2,碱性磷酸酶,骨唾液蛋白和骨钙素的基因表达上调。 ERRM和ProRoot-MTA均可增强MSC的成骨分化。

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