Downregulation of lncRNA DANCR promotes osteogenic differentiation of periodontal ligament stem cells.

Q2 Biochemistry, Genetics and Molecular Biology
Zhuo Wang, Yuanliang Huang, Luanjun Tan
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引用次数: 17

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

Abstract Image

Abstract Image

Abstract Image

lncRNA DANCR下调促进牙周韧带干细胞成骨分化。
背景:长链非编码rna (Long non-coding RNAs, lncRNAs)在生理和病理方面具有显著的作用。在牙齿再生中,牙周韧带干细胞(periodontal ligament stem cells, PDLSCs)被认为是一个关键的效应因子,然而lncRNA在PDLSCs成骨分化中的作用机制尚不完全清楚。本研究旨在发现lncRNA DANCR与PDLSCs增殖及成骨分化的关系。方法:采用芯片技术观察lncrna在分化和未分化PDLSCs中的表达差异。然后筛选出与成骨相关的lncRNA, DANCR。通过构建过表达抑制模型,探讨其对细胞增殖和成骨分化的影响。采用qRT-PCR检测成骨相关基因mRNA表达。MTT法评价DANCR对细胞生长曲线的影响。为了量化DANCR对PDLSCs成骨分化的影响,在基础培养基和成骨培养基中进行ALP染色和茜素红染色。对数据进行统计学处理。结果:与未分化的PDLSCs相比,分化后的PDLSCs茜素红染色水平较高。成骨分化标志基因runt相关转录因子2 (Runx2)、骨钙素(OCN)、骨形态发生蛋白(BMP-2)在分化后的PDLSCs中表达显著升高。此外,我们注意到与对照组相比,lncRNA DANCR的表达在成骨诱导的PDLSCs中显著降低。DANCR促进PDLSCs的增殖,正如细胞活力所证明的那样。进一步研究证实,DANCR的下调表现在钙沉积的形成、碱性磷酸酶(ALP)的激活以及Runx2、OCN、BMP-2等成骨相关基因标记物的上调,最终导致PDLSCs经转染诱导后向成骨分化。相反,DANCR上调被证明抑制PDLSCs的成骨分化潜能。结论:PDLSCs的成骨分化与lncRNA DANCR的下调有关。阐明了DANCR在PDLSCs成骨分化过程中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Developmental Biology
BMC Developmental Biology 生物-发育生物学
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Developmental Biology is an open access, peer-reviewed journal that considers articles on the development, growth, differentiation and regeneration of multicellular organisms, including molecular, cellular, tissue, organ and whole organism research.
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