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Effect of fibroblast growth factor-2 on periodontal ligament cells derived from human deciduous teeth in vitro

机译:成纤维细胞生长因子2对人乳牙来源的牙周膜细胞的影响

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摘要

A blood supply is crucial for tissue healing and regeneration. Periodontal ligament (PDL) tissue is situated between the tooth root and alveolar bone, and cells derived from PDL tissue are reported to have stem cell-like activity. This study aimed to evaluate the potential of PDL cells derived from deciduous teeth to express endothelial cell (EC)-specific markers. Using quantitative PCR, we investigated whether PDL cells derived from human deciduous teeth express mRNA for the EC-specific markers: vascular endothelialcadherin (VE-cadherin), vascular endothelial growth factor receptor 2 (VEGFR2) and CD31 upon treatment with 15 ng/ml heparin or 10 ng/ml fibroblast growth factor (FGF)-2 in vitro. Quantitative PCR showed that PDL cells expressed mRNA for the EC-specific markers, VE-cadherin and VEGFR2, when cultured in the presence of heparin alone or with FGF-2. By contrast, marked CD31 mRNA expression was induced only when PDL cells were cultured with both heparin and FGF-2. Western blot analysis showed that the CD31 protein was induced in PDL cells upon treatment with both heparin and FGF-2 for 3 weeks. PDL cells derived from deciduous teeth inducibly express EC-specific markers and thus have the potential to differentiate into a vascular cell lineage.
机译:血液供应对于组织愈合和再生至关重要。牙周膜(PDL)组织位于牙根和牙槽骨之间,据报道,源自PDL组织的细胞具有干细胞样活性。这项研究旨在评估源自乳牙的PDL细胞表达内皮细胞(EC)特异性标记的潜力。使用定量PCR,我们研究了用15 ng / ml肝素处理的人乳牙衍生的PDL细胞是否表达EC特异性标志物的mRNA:血管内皮钙粘蛋白(VE-cadherin),血管内皮生长因子受体2(VEGFR2)和CD31。或体外10 ng / ml成纤维细胞生长因子(FGF)-2。定量PCR显示,当在单独的肝素存在下或与FGF-2一起培养时,PDL细胞表达EC特异性标记VE-钙粘着蛋白和VEGFR2的mRNA。相比之下,只有当PDL细胞与肝素和FGF-2一起培养时,才会诱导明显的CD31 mRNA表达。 Western印迹分析表明,用肝素和FGF-2处理3周后,在PDL细胞中诱导了CD31蛋白。源自乳牙的PDL细胞可诱导表达EC特异性标记,因此具有分化为血管细胞谱系的潜力。

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