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首页> 外文期刊>BMC Developmental Biology >Downregulation of lncRNA DANCR promotes osteogenic differentiation of periodontal ligament stem cells
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Downregulation of lncRNA DANCR promotes osteogenic differentiation of periodontal ligament stem cells

机译:LNCRNA DANCR的下调促进牙周韧带干细胞的成骨分化

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Long non-coding RNAs (lncRNAs) have been widely known to have an appreciable effect in physiology and pathology. In tooth regeneration, periodontal ligament stem cells (PDLSCs) are regarded as a key effector, whereas, how lncRNA acts in the osteogenic differentiation of PDLSCs have not been completely understood. This study aims to find out the relationship between lncRNA DANCR and the proliferation and osteogenic differentiation of PDLSCs. Microarray was used to observe the different expression of lncRNAs in differentiated and undifferentiated PDLSCs. And then osteogenic-related lncRNA, DANCR was screened out. Its effects on proliferation and osteogenic differentiation was explored?by constructing an overexpression and inhibition model. qRT-PCR was used to detect the mRNA expression of osteogenesis related genes. MTT assay was performed to assess the effects of DANCR on cell growth curve. To quantify the effects of DANCR on osteogenic differentiation of PDLSCs, ALP staining and alizarin red was performed in basic culture medium and osteogenic medium. Data were statistically processed. Compared with the undifferentiated PDLSCs, the alizarin red staining level was higher in differentiated PDLSCs. And the expressions of osteogenic differentiation marker genes Runt-related transcription factor 2 (Runx2), osteocalcin (OCN) and bone morphogenetic protein (BMP-2) were significantly increased in the differentiated PDLSCs. Furthermore, we noticed that comparing with control groups, the expression of lncRNA DANCR decreases markedly in osteogenically induced PDLSCs. DANCR promoted proliferation of PDLSCs, as evidenced by cell viability. Further investigation has proven that the downregulation of DANCR shows in the calcium sediment forming, alkaline phosphatase (ALP) activation and some osteogenic-related gene markers’ upregulation including Runx2, OCN and BMP-2, which finally results in the osteogenic differentiation of PDLSCs following the transfection and induction. Conversely, DANCR upregulation was shown to repress the osteogenic differentiation potential of PDLSCs. The osteogenic differentiation of PDLSCs has proven to related to the down regulation of lncRNA DANCR. And this paper throws light on the effects of DANCR in the process of PDLSCs’ osteogenic differentiation.
机译:广泛众所周知,长期非编码RNA(LNCRNA)对生理和病理学具有明显的影响。在牙齿再生中,牙周韧带干细胞(PDLSCs)被认为是关键效应器,而LNCRNA如何作用于PDLSC的成骨分化,尚未完全理解。本研究旨在了解LNCRNA丹麦(LNCRNA DANCR)与PDLSCs的增殖和成骨分化之间的关系。微阵列用于观察分化和未分化的PDLSC中LNCRNA的不同表达。然后筛选出骨质发生相关的LNCRNA,达到丹麦克。探索其对增殖和骨质发生分化的影响?通过构建过表达和抑制模型。 QRT-PCR用于检测骨发生相关基因的mRNA表达。进行MTT测定以评估DANCR对细胞生长曲线的影响。为了量化DANCR对PDLSCs的骨质发生分化的影响,在碱性培养基和骨质发生培养基中进行ALP染色和茜素红。数据在统计上处理。与未分化的PDLSC相比,分化的PDLSCs茜素红染色水平较高。并且在分化的PDLSCs中显着增加了与骨质发生分化标志物基因的r型相关转录因子2(RUNX2),骨钙素(OCN)和骨形态发生蛋白(BMP-2)显着增加。此外,我们注意到与对照组进行比较,在骨开诱导的PDLSCs中,LNCRNA DANCR的表达明显减少。 DANCR促进了PDLSC的增殖,如细胞活力所证明。进一步的调查证明,DANCR的下调显示在钙沉积物形成,碱性磷酸酶(ALP)活化和一些骨质发生相关基因标志物的上调,包括RUNX2,OCN和BMP-2,最终导致PDLSCs的成骨分化转染和诱导。相反,显示DANCR上调,抑制了PDLSC的骨质化分化潜力。 PDLSCs的骨质发生分化已被证明与LNCRNA DANCR的下调调节有关。本文在PDLSCS'osteogenic分化过程中抛出了DANCR的影响。

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