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首页> 外文期刊>Biochemical and Biophysical Research Communications >Upregulation of dentin matrix protein 1 promoter activities by core binding factor alpha 1 in human dental pulp stem cells
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Upregulation of dentin matrix protein 1 promoter activities by core binding factor alpha 1 in human dental pulp stem cells

机译:牙髓干细胞中核心结合因子α1上调牙本质基质蛋白1启动子的活性

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摘要

An osteoblast-specific transcription factor, core binding factor alpha 1 (Cbf alpha 1), is critical for osteoblast and odontoblast differentiation. In this study, the role of Cbf alpha 1 in human dentin matrix protein1 (DMP1) gene expression in human dental pulp stem cells (HDPSCs) was investigated. The desired promoter fragments were obtained and cloned into the pGL3-basic vector. It was found that Cbf alpha 1 isoforms were predominantly expressed in the cytoplasm of the HDPSCs and reached to the maximum after transfection for 48 h. Furthermore, forced overexpression of Cbf alpha 1 induced the increase of the luciferase activities of pGL3-P1-6, especially those of pGL3-P-505to+86 (p < 0.05) were the most significant. Then the site-directed mutagenesis of Cbf alpha 1 binding sites in the promoter region of nt -505 to +86 resulted in a marked decline of luciferase activities. Thus, our results suggest that Cbf alpha 1 upregulates DMP1 gene expression differentially that may contribute to the spatial-temporal expression pattern of DMP1 during odontoblast differentiation. Published by Elsevier Inc.
机译:成骨细胞特异性转录因子,核心结合因子α1(Cbf alpha 1),对于成骨细胞和成牙本质细胞的分化至关重要。在这项研究中,研究了Cbf alpha 1在人类牙髓干细胞(HDPSC)中人类牙本质基质蛋白1(DMP1)基因表达中的作用。获得所需的启动子片段,并将其克隆到pGL3-碱性载体中。发现Cbf alpha 1亚型主要在HDPSC的细胞质中表达,转染48 h后达到最大。此外,强迫过表达Cbf alpha 1诱导了pGL3-P1-6荧光素酶活性的增加,尤其是pGL3-P-505to + 86的荧光素酶活性的增加(p <0.05)。然后定点诱变的Cbf alpha 1绑定站点在nt -505到+86的启动子区域导致荧光素酶活性明显下降。因此,我们的结果表明Cbf alpha 1差异性上调DMP1基因表达,这可能有助于成牙本质细胞分化过程中DMP1的时空表达模式。由Elsevier Inc.发布

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