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Screening the Expression Changes in MicroRNAs and Their Target Genes in Mature Cementoblasts Stimulated with Cyclic Tensile Stress

机译:筛选在周期性拉伸应力刺激下成熟的成骨细胞中microRNA及其靶基因表达的变化

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摘要

Cementum is a thin layer of cementoblast-produced mineralized tissue covering the root surfaces of teeth. Mechanical forces, which are produced during masticatory activity, play a paramount role in stimulating cementoblastogenesis, which thereby facilitates the maintenance, remodeling and integrity of cementum. However, hitherto, the extent to which a post-transcriptional modulation mechanism is involved in this process has rarely been reported. In this study, a mature murine cementoblast cell line OCCM-30 cells (immortalized osteocalcin positive cementoblasts) was cultured and subjected to cyclic tensile stress (0.5 Hz, 2000 µstrain). We showed that the cyclic tensile stress could not only rearrange the cell alignment, but also influence the proliferation in an S-shaped manner. Furthermore, cyclic tensile stress could significantly promote cementoblastogenesis-related genes, proteins and mineralized nodules. From the miRNA array analyses, we found that 60 and 103 miRNAs were significantly altered 6 and 18 h after the stimulation using cyclic tensile stress, respectively. Based on a literature review and bioinformatics analyses, we found that miR-146b-5p and its target gene Smad4 play an important role in this procedure. The upregulation of miR-146b-5p and downregulation of Smad4 induced by the tensile stress were further confirmed by qRT-PCR. The direct binding of miR-146b-5p to the three prime untranslated region (3' UTR) of Smad4 was established using a dual-luciferase reporter assay. Taken together, these results suggest an important involvement of miR-146b-5p and its target gene Smad4 in the cementoblastogenesis of mature cementoblasts.
机译:牙骨质是覆盖牙根表面的由成骨细胞产生的矿化组织的薄层。在咀嚼活动期间产生的机械力在刺激牙骨质形成中起着至关重要的作用,从而促进牙骨质的维持,重塑和完整性。然而,迄今为止,很少报道转录后调节机制参与该过程的程度。在这项研究中,培养了成熟的鼠成牙本质细胞系OCCM-30细胞(永生化骨钙素阳性成牙本质细胞)并受到循环拉伸应力(0.5 Hz,2000 µstrain)。我们表明,循环拉伸应力不仅可以重新排列细胞排列,而且可以以S形方式影响增殖。此外,循环拉伸应力可以显着促进与成骨细胞生成有关的基因,蛋白质和矿化的结节。从miRNA阵列分析中,我们发现使用循环拉伸应力刺激后6和18 h,分别有60和103个miRNA发生了显着改变。根据文献综述和生物信息学分析,我们发现miR-146b-5p及其靶基因Smad4在此过程中起重要作用。通过qRT-PCR进一步证实了由拉应力诱导的miR-146b-5p的上调和Smad4的下调。使用双荧光素酶报告基因测定,确定了miR-146b-5p与Smad4的三个主要非翻译区(3'UTR)的直接结合。综上所述,这些结果表明miR-146b-5p及其靶基因Smad4参与了成熟成牙本质细胞的成骨细胞形成。

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