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微小RNA-140-5p介导的人牙髓干细胞增殖和分化调控通过脂多糖/ toll样受体4信号通路发生。

miR-140-5p-mediated regulation of the proliferation and differentiation of human dental pulp stem cells occurs through the lipopolysaccharide/toll-like receptor 4 signaling pathway.

作者信息

Sun De-Gang, Xin Bing-Chang, Wu Di, Zhou Lei, Wu Hong-Bin, Gong Wen, Lv Jian

机构信息

Department of Cariology and Endodontology, Qingdao Stomatological Hospital, Qingdao, Shandong, China.

Department of Preventive Dentistry, Qingdao Stomatological Hospital, Qingdao, Shandong, China.

出版信息

Eur J Oral Sci. 2017 Dec;125(6):419-425. doi: 10.1111/eos.12384.

Abstract

Human dental pulp stem cells (DPSCs) are oral mesenchymal stem cells with potential to differentiate into various cell types. Recent studies of DPSCs have focused on microRNAs (miRNAs), a class of small noncoding RNAs that play crucial roles in regulating DPSC phenotypes. In the current study, the expression of miR-140-5p was significantly decreased during lipopolysaccharide (LPS)-mediated differentiation of DPSCs in vitro. Overexpression of miR-140-5p enhanced proliferation of DPSCs and inhibited DPSC differentiation, whereas suppression of miR-140-5p produced the opposite effect. Moreover, the expression of toll-like receptor 4 (TLR-4), a critical regulator of DPSCs, was negatively correlated with the levels of miR-140-5p. A luciferase reporter analysis confirmed that miR-140-5p could regulate TLR-4 by directly binding to the 3'-untranslated region (3'-UTR) of the TLR4 mRNA. Additionally, we suppressed TLR-4 expression by treating cells with a TLR-4 inhibitor, CLI-095, and demonstrated that the effect of the miR-140-5p inhibitor on DPSC proliferation and differentiation could be partially reversed by blocking TLR-4. Taken together, our data suggest that miR-140-5p is a novel miRNA that regulates DPSC proliferation and differentiation.

摘要

人牙髓干细胞(DPSCs)是具有分化为多种细胞类型潜能的口腔间充质干细胞。近期对DPSCs的研究聚焦于微小RNA(miRNAs),这是一类在调节DPSC表型中起关键作用的小型非编码RNA。在本研究中,在脂多糖(LPS)介导的DPSCs体外分化过程中,miR-140-5p的表达显著降低。miR-140-5p的过表达增强了DPSCs的增殖并抑制了DPSC的分化,而抑制miR-140-5p则产生相反的效果。此外,Toll样受体4(TLR-4)作为DPSCs的关键调节因子,其表达与miR-140-5p的水平呈负相关。荧光素酶报告基因分析证实,miR-140-5p可通过直接结合TLR4 mRNA的3'-非翻译区(3'-UTR)来调节TLR-4。此外,我们用TLR-4抑制剂CLI-095处理细胞以抑制TLR-4表达,并证明通过阻断TLR-4可部分逆转miR-140-5p抑制剂对DPSC增殖和分化的影响。综上所述,我们的数据表明miR-140-5p是一种调节DPSC增殖和分化的新型miRNA。

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