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首页> 外文期刊>Archives of Oral Biology >Effects of Notch ligand Delta1 on the proliferation and differentiation of human dental pulp stem cells in vitro.
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Effects of Notch ligand Delta1 on the proliferation and differentiation of human dental pulp stem cells in vitro.

机译:Notch配体Delta1对人牙髓干细胞体外增殖和分化的影响。

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OBJECTIVE: Notch signalling controls cell fate decisions in adult and embryonic tissues. The Notch ligand Delta1 is known to influence proliferation and differentiation of many kinds of tissue specific stem cells. In the present study, we investigated the role of Delta1 in the regulation of dental pulp stem cells (DPSCs) in vitro. METHODS: DPSCs were isolated from impacted third molars. Expression of human Notch1, 2 and Delta1 in DPSCs were detected by immunochemistry. Delta1 overexpressed DPSCs were constructed by a retroviral method. Delta1 transduced DPSCs proliferation changes were examined by means of colony-forming assay, BrdU incorporation assay and cell cycle analysis. Delta1 transduced DPSCs were cultured in differentiation-inductive medium. The nodule formation and DSPP expression were evaluated. RESULTS: It was shown that the Notch receptors and Delta1 ligand were expressed throughout the proliferation and differentiation process of cultured dental pulp stem cells. Furthermore, it was found in our study that Delta1 could significantly enhance the proliferation of DPSCs and permit DPSCs differentiating into odontoblast-like cells in differentiation-inductive environments. CONCLUSIONS: Our findings verified that Notch-Delta1 signalling was expressed in human DPSCs in vitro and appeared to play pivotal role in DPSCs proliferation enhancement and differentiation regulation, thereby consistent with the hypothesis that the Notch pathway controls stem cell fate during pulp regeneration.
机译:目的:Notch信号控制成人和胚胎组织中的细胞命运决定。已知Notch配体Delta1可影响多种组织特异性干细胞的增殖和分化。在本研究中,我们调查了Delta1在体外牙髓干细胞(DPSCs)调控中的作用。方法:从受影响的第三磨牙中分离出DPSC。通过免疫化学检测人Notch1、2和Delta1在DPSC中的表达。通过逆转录病毒方法构建了Delta1过表达的DPSC。通过集落形成测定,BrdU掺入测定和细胞周期分析检查了Delta1转导的DPSC的增殖变化。在分化诱导培养基中培养Delta1转导的DPSC。评价结节形成和DSPP表达。结果:Notch受体和Delta1配体在培养的牙髓干细胞的增殖和分化过程中均表达。此外,在我们的研究中发现,Delta1可以显着增强DPSC的增殖,并允许DPSC在诱导分化的环境中分化为成牙本质细胞样细胞。结论:我们的研究结果证实了Notch-Delta1信号在人DPSCs中体外表达,并在DPSCs增殖增强和分化调节中起着关键作用,从而与Notch通路在牙髓再生过程中控制干细胞命运的假设相符。

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