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Dynamic Expression Profiles of Marker Genes in Osteogenic Differentiation of Human Bone Marrow-derived Mesenchymal Stem Cells

机译:标记基因在人骨髓间充质干细胞成骨分化中的动态表达谱

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摘要

Objective To observe the expression profiles of osteoblast-related genes in human mesenchymal stem cells (MSCs) derived from bone marrow during osteogenic differentiation. Methods MSCs were induced to differentiate with MSC osteogenic differentiation medium for 7, 14, 21 and 28 days respectively. Alizarin Red staining was used to detect matrix mineralization. Expression of osteoblast-related genes, including osteocalcin, osteopontin, Runt-related transcription factor 2 (Runx2), alkaline phosphatase and collagen type Ⅰ, was assessed with quantitative reverse transcription-polymerase chain reaction. Results On day 14 after induction of differentiation, cells were stained positively with Alizarin Red. The expression levels of these genes exhibited an upward trend as induction time was prolonged. Exposure to osteogenic differentiation medium less than 21 days did not significantly induce osteocalcin expression;osteocalcin expression levels in the differentiated cells induced for 21 and 28 days were 1.63 and 2.46 times as high as the undifferentiated cells respectively (all P<0.05). Stimulation with MSC osteogenic differentiation medium over 14 days significantly enhanced bone marrow-derived MSCs to express osteopontin and Runx2 genes (all P<0.05). Osteogenic differentiation medium could significantly induce the expressions of alkaline phosphatase and collagen typeⅠ genes (all P<0.05). Their expressions reached the peak levels on day 21, which were increased more than 4-and 3-fold respectively. Conclusion Human bone marrow-derived MSCs could exhibit the sequential expression pattern of osteoblast marker genes during osteogenic differentiation in vitro.
机译:目的观察成骨相关基因在人骨髓间充质干细胞(MSCs)成骨分化过程中的表达情况。 方法分别用MSC成骨分化培养基诱导MSC分化7、14、21和28天。茜素红染色用于检测基质矿化。用定量逆转录-聚合酶链反应检测成骨细胞相关基因的表达,包括骨钙素,骨桥蛋白,Runt相关转录因子2(Runx2),碱性磷酸酶和Ⅰ型胶原。 结果在诱导分化后的第14天,用茜素红对细胞进行了阳性染色。随着诱导时间的延长,这些基因的表达水平呈上升趋势。暴露于成骨分化培养基少于21天时,未显着诱导骨钙素表达;诱导21和28天的分化细胞中骨钙素表达水平分别是未分化细胞的1.63倍和2.46倍(所有P <0.05)。用MSC成骨分化培养基刺激14天可显着增强骨髓来源的MSC表达骨桥蛋白和Runx2基因的表达(所有P <0.05)。成骨分化培养基能明显诱导碱性磷酸酶和Ⅰ型胶原基因的表达(均P <0.05)。他们的表达在第21天达到峰值,分别增加了4倍和3倍以上。 结论结论人骨髓间充质干细胞在成骨分化过程中可能表现出成骨细胞标记基因的顺序表达模式。

著录项

  • 来源
    《中国医学科学杂志(英文版)》 |2015年第2期|108-113|共6页
  • 作者单位

    Department of 0rthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of 0rthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of 0rthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of 0rthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of 0rthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-19 03:38:37
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