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Expression of MicroRNA-30c and its Target Genes by nano-Bioglass Ceramic-treatment in Human Osteoblastic Cells

机译:用纳米生物制剂陶瓷治疗在人骨细胞中的纳米生物糖类陶瓷治疗的表达

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摘要

Osteoblast differentiation is tightly regulated by transcriptional regulators such as microRNAs (miRNAs). Several bioactive materials including nano-bioglass ceramic particles (nBGC) influence differentiation of the osteoblasts, but the molecular mechanisms of nBGC-stimulation of osteoblast differentiation via miRNAs are not yet known. In this study, we identified that nBGC-treatment stimulated expression of miR-30c in human osteoblastic cells (MG63). The bioinformatics tools identified its regulatory network, molecular function, biological process and its target genes involved in negative regulation of osteoblast differentiation. TGIF2 and HDAC4 were found to be its putative target genes and they were down regulated by nBGC-treatment in MG63 cells. Thus, this study advances our understanding of nBGC action on bone cells and supports utilization of nBGC in bone tissue engineering.
机译:成骨细胞的分化受到转录调节剂如microRNA(miRNA)的严格调控。包括纳米生物玻璃陶瓷颗粒(nBGC)在内的几种生物活性材料会影响成骨细胞的分化,但是nBGC刺激通过miRNA刺激成骨细胞分化的分子机制尚不清楚。在这项研究中,我们确定nBGC处理刺激了人类成骨细胞(MG63)中miR-30c的表达。生物信息学工具确定了其调控网络,分子功能,生物学过程以及涉及成骨细胞分化负调控的靶基因。 TGIF2和HDAC4被发现是其推定的靶基因,并且在MG63细胞中被nBGC处理下调。因此,这项研究提高了我们对nBGC对骨细胞作用的理解,并支持nBGC在骨组织工程中的利用。

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