UCL Centre for Biomaterials in Surgical Reconstruction and Regeneration, Division of Surgery & Interventional Science, University College London, London NW3 2PF, UK.
UCL Institute of Orthopaedics and Musculoskeletal Science, Division of Surgery & Interventional Science, University College London, Stanmore, London HA7 4AP, UK.
Int J Mol Sci. 2021 Jun 17;22(12):6505. doi: 10.3390/ijms22126505.
: Applying mesenchymal stem cells (MSCs), together with the distraction osteogenesis (DO) process, displayed enhanced bone quality and shorter treatment periods. The DO guides the differentiation of MSCs by providing mechanical clues. However, the underlying key genes and pathways are largely unknown. The aim of this study was to screen and identify hub genes involved in distraction-induced osteogenesis of MSCs and potential molecular mechanisms. The datasets were downloaded from the ArrayExpress database. Three samples of negative control and two samples subjected to 5% cyclic sinusoidal distraction at 0.25 Hz for 6 h were selected for screening differentially expressed genes (DEGs) and then analysed via bioinformatics methods. The Gene Ontology (GO) terms and Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway enrichment were investigated. The protein-protein interaction (PPI) network was visualised through the Cytoscape software. Gene set enrichment analysis (GSEA) was conducted to verify the enrichment of a self-defined osteogenic gene sets collection and identify osteogenic hub genes. Three hub genes (, , and ) that were highly associated with distraction-induced osteogenesis of MSCs were identified via the Venn diagram. These hub genes could provide a new understanding of distraction-induced osteogenic differentiation of MSCs and serve as potential gene targets for optimising DO via targeted therapies.
应用间充质干细胞(MSCs)并结合牵张成骨(DO)过程可提高骨质量并缩短治疗周期。DO 通过提供机械线索来指导 MSCs 的分化。然而,其潜在的关键基因和途径在很大程度上尚不清楚。本研究旨在筛选和鉴定与 MSC 牵张诱导成骨相关的枢纽基因及潜在的分子机制。从 ArrayExpress 数据库下载数据集。选择三个阴性对照样本和两个在 0.25 Hz 下进行 5%循环正弦牵张 6 小时的样本进行差异表达基因(DEG)筛选,然后通过生物信息学方法进行分析。研究了基因本体论(GO)术语和京都基因与基因组百科全书(KEGG)途径富集。通过 Cytoscape 软件可视化蛋白质-蛋白质相互作用(PPI)网络。通过基因集富集分析(GSEA)验证了自我定义的成骨基因集集合的富集情况,并确定了成骨枢纽基因。通过 Venn 图鉴定出三个与 MSC 牵张诱导成骨高度相关的枢纽基因(、和)。这些枢纽基因可以为理解 MSC 牵张诱导成骨分化提供新的认识,并为通过靶向治疗优化 DO 提供潜在的基因靶点。