Differential circRNA expression profiles during the BMP2-induced osteogenic differentiation of MC3T3-E1 cells

骨形态发生蛋白2 小桶 小RNA 生物 运行x2 细胞生物学 成骨细胞 碱性磷酸酶 核糖核酸 基因 环状RNA 细胞分化 基因表达 分子生物学 转录组 体外 遗传学 生物化学 酶
作者
Dongyang Qian,Guang-Bin Yan,Bo Bai,Yi Chen,Shujiang Zhang,Yongchang Yao,Hong Xia
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier BV]
卷期号:90: 492-499 被引量:84
标识
DOI:10.1016/j.biopha.2017.03.051
摘要

Abstract Objective Recent studies have indicated that circular RNAs (circRNAs) might play important roles in various diseases. However, little is known about the functions of circRNAs in the skeletal system, and the role of circRNAs in the mechanism by which bone morphogenetic protein 2 (BMP2) promotes bone differentiation remains unknown. Here, we performed RNA-seq to analyze differential expression of circRNA during different osteoblast differentiation stages and investigated the relevant mechanisms. Materials and methods Alkaline phosphatase (ALP) staining and activity were performed to assess osteogenic differentiation in MC3T3-E1 cells. The expression of osteogenic markers in MC3T3-E1 cells and the differential expression levels of circRNAs were measured and validated by qRT-PCR. Osteogenic marker proteins were measured by western blot. RNA-seq was performed to detect differential expression of circRNAs during the osteogenic differentiation of MC3T3-E1 cells induced by BMP2. Gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) and PANTHER pathway analyses were performed to predict the functions of differentially expressed circRNAs and potentially co-expressed target genes. The microRNA (miRNA) targets of the circRNAs and circRNA–miRNA interactions were predicted by miRanda. The circRNA–miRNA co-expression network was constructed based on the correlation analysis between the differentially expressed circRNAs and miRNAs. A graph of the circRNA–miRNA network was created using Cytoscape 3.01. Results The Cell Counting Kit 8 (CCK-8) assay showed that BMP2 promoted the proliferation of osteoblasts in vitro . Both the intracellular ALP content and activity were increased in BMP2-treated MC3T3-E1 cells. In addition, the mRNA and protein levels of the osteoblastic markers ALP, Sp7 transcription factor (SP7) and runt-related transcription factor 2 (RUNX2) were substantially up-regulated. In the present study, 158 circRNAs were differentially expressed by a fold-change ≥2.0, P Conclusion The present study identified circ19142 and circ5846 as being associated with osteoblast differentiation and BMP2 may induce osteogenic differentiation through a circ19142/circ5846-targeted miRNA–mRNA axis.
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