梁莉, 余继锋, 周威, 刘洪臣. 内皮素-1对牙周膜干细胞成骨分化能力的影响[J]. 解放军医学院学报, 2016, 37(9): 988-991. DOI: 10.3969/j.issn.2095-5227.2016.09.019
引用本文: 梁莉, 余继锋, 周威, 刘洪臣. 内皮素-1对牙周膜干细胞成骨分化能力的影响[J]. 解放军医学院学报, 2016, 37(9): 988-991. DOI: 10.3969/j.issn.2095-5227.2016.09.019
LIANG Li, YU Jifeng, ZHOU Wei, LIU Hongchen. Effect of endothelin-1 on osteogenic differentiation of human periodontal ligament stem cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(9): 988-991. DOI: 10.3969/j.issn.2095-5227.2016.09.019
Citation: LIANG Li, YU Jifeng, ZHOU Wei, LIU Hongchen. Effect of endothelin-1 on osteogenic differentiation of human periodontal ligament stem cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(9): 988-991. DOI: 10.3969/j.issn.2095-5227.2016.09.019

内皮素-1对牙周膜干细胞成骨分化能力的影响

Effect of endothelin-1 on osteogenic differentiation of human periodontal ligament stem cells

  • 摘要: 目的 研究内皮素-1(endothelin-1,ET-1)对牙周膜干细胞(periodontal ligament stem cells,PDLSCs)成骨分化能力的影响。 方法 体外培养鉴定牙周膜干细胞,加入不同浓度(10-9mol/L、10-8mol/L、10-7mol/L)的ET-1培养7 d、14 d、21 d,通过实时定量PCR及Western blot检测PDLSCs成骨关键蛋白/基因(Runx2、OCN、COL1)的变化,确定ET-1在PDLSCs成骨分化中的作用。 结果 在ET-1刺激下,牙周膜干细胞Runx2、OCN和COL1 mRNA及蛋白表达水平逐渐升高,在21 d时达到最高值。在7 d、14 d和21 d,ET-1(10-9mol/L、10-8mol/L、10-7mol/L)剂量依赖性地促进牙周膜干细胞Runx2、OCN和COL1 mRNA及蛋白表达的上调。 结论 内皮素-1可促进牙周膜干细胞的成骨分化能力。

     

    Abstract: Objective To investigate the effect of endothelin-1 on osteogenic differentiation in human periodontal ligament stem cells (PDLSCs). Methods PDLSCs were isolated from the periodontal ligament tissues of patients and then were treated with ET-1 (10-9, 10-8or 10-7mol/L) for 7 d, 14 d, or 21 d.mRNA and protein expressions of Runx2, OCN, and COL1 were detected by real time PCR and western blot, respectively, and the role of ET-1 in osteogenic differentiation of PDLSCs was identified. Results The mRNA and protein expression of Runx2, OCN, and COL1gradually increased with the exposure of ET-1, peaking at day 21 (P< 0.05).At each time point (7 d, 14 d, and 21 d), the mRNA and protein expressions of Runx2, OCN, and COL1 were induced at a dose-dependent manner (10-9, 10-8or 10-7mol/L). Conclusion ET-1 may promote osteogenic differentiation of PDLSCs by increasing expression of Runx2, OCN, and COL1.

     

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