The State Key Laboratory of Oral Diseases, Sichuan University, Chengdu, 610041, People's Republic of China.
Department of Oral and Maxillofacial Surgery, West China College of Stomatology, Sichuan University, Chengdu, 610041, People's Republic of China.
Calcif Tissue Int. 2018 Sep;103(3):338-352. doi: 10.1007/s00223-018-0426-0. Epub 2018 Apr 26.
Osteogenesis is a complex and tightly regulated process. Circular RNAs (circRNAs) are covalently closed RNA molecules which are thought to play a significant role in bone metabolism. The purpose of this study was to investigate the expression and putative function of circRNAs during the osteogenic differentiation of mouse adipose-derived stromal cells (mADSCs). circRNA microarrays were used to determine differential circRNAs expression at different stages during osteogenesis of mADSCs. The most frequent differentially expressed circRNAs were selected by Venn analysis and clustered among the three induced groups. In addition, bioinformatic analyses (gene ontology, pathway, and co-expression network analysis) were used to further investigate these differentially expressed circRNAs. A total of 14,236 circRNAs were detected, of which 43 circRNAs (40 upregulated) were consistently altered at indicated time points during osteogenic differentiation of mADSCs. The exonic circRNAs represented a significantly larger proportion among the differentially expressed circRNAs compared to other types of circRNAs. Gene ontology and Kyoto Encyclopedia of Genes and Genomes biological pathway analysis were performed to evaluate the functions of differentially expressed circRNAs during the osteogenic process. Our circRNA-miRNA co-expression network showed that miR-338-3p was correlated with upregulation of two circRNAs (mmu_circRNA_013422, mmu_circRNA_22566). Our data on circRNA expression profiles may provide valuable insight into circRNA function during osteogenic differentiation of mADSCs. Additionally, the circRNA-miRNA-mRNA pathways may provide information on novel mechanisms and targets for clinical investigations on bone formation and regeneration.
成骨作用是一个复杂且受到严密调控的过程。环状 RNA(circRNA)是共价封闭的 RNA 分子,被认为在骨代谢中发挥重要作用。本研究旨在探讨环状 RNA 在小鼠脂肪基质细胞(mADSCs)成骨分化过程中的表达及其潜在功能。使用环状 RNA 微阵列确定 mADSCs 成骨分化不同阶段的差异表达环状 RNA。通过 Venn 分析选择最频繁差异表达的环状 RNA,并在三个诱导组中进行聚类。此外,还进行了生物信息学分析(基因本体、途径和共表达网络分析),以进一步研究这些差异表达的环状 RNA。共检测到 14236 个环状 RNA,其中 43 个环状 RNA(40 个上调)在 mADSCs 成骨分化的各个时间点均发生改变。与其他类型的环状 RNA 相比,外显子环状 RNA 在差异表达的环状 RNA 中所占比例显著更高。进行基因本体和京都基因与基因组百科全书生物途径分析,以评估差异表达的环状 RNA 在成骨过程中的功能。我们的环状 RNA-miRNA 共表达网络显示,miR-338-3p 与两个环状 RNA(mmu_circRNA_013422、mmu_circRNA_22566)的上调相关。我们关于环状 RNA 表达谱的数据可能为 mADSCs 成骨分化过程中环状 RNA 功能提供有价值的见解。此外,环状 RNA-miRNA-mRNA 途径可能为骨形成和再生的临床研究提供关于新机制和靶点的信息。