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SP1 promotes the odontoblastic differentiation of dental papilla cells

机译:SP1促进牙乳头细胞的牙本质成骨细胞分化

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摘要

Odontoblasts are a type of terminally differentiated and matrix-secreting cells that are responsible for dentinogenesis. The process of odontoblast differentiation is regulated by a variety of transcription factors. The transcription factor SP1 is known to play an essential regulatory role in cell proliferation and differentiation. The purpose of this study was to investigate the role of SP1 in odontoblastic differentiation. Immunohistochemistry verified that SP1 was specifically expressed in polarizing and secretory odontoblasts invivo. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunofluorescence revealed that the expression of SP1 was significantly upregulated during odontoblastic differentiation of mDPC6T cells, a dental papilla cell line. Overexpression of SP1 significantly increased the expression of odontoblast-related genes, including DSPP, DMP1 and ALP, and promoted the formation of mineralized nodules. Meanwhile, knockdown of SP1 decreased the expression of these odontoblast-related genes and suppressed the formation of mineralized nodules. Our results demonstrate that SP1 promotes the odontoblastic differentiation and mineralization of dental papilla cells.
机译:成牙本质细胞是负责牙本质生成的终末分化和基质分泌细胞的一种。成牙本质细胞分化过程受多种转录因子调控。已知转录因子SP1在细胞增殖和分化中起着重要的调节作用。这项研究的目的是调查SP1在成牙本质细胞分化中的作用。免疫组织化学证实SP1在成极化和分泌性成牙本质细胞体内特异性表达。定量逆转录-聚合酶链反应(qRT-PCR)和免疫荧光显示,在牙乳头细胞系mDPC6T细胞的牙母质分化过程中,SP1的表达明显上调。 SP1的过表达显着增加了成牙本质细胞相关基因(包括DSPP,DMP1和ALP)的表达,并促进了矿化结节的形成。同时,敲低SP1会减少这些成牙本质细胞相关基因的表达并抑制矿化结节的形成。我们的结果表明,SP1促进牙乳头细胞的牙本质成骨细胞分化和矿化。

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