Liu Fanxiao, Dong Jun, Zhang Peng, Zhou Dongsheng, Zhang Qingyu
Department of Orthopaedics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Front Mol Biosci. 2022 Feb 11;8:782054. doi: 10.3389/fmolb.2021.782054. eCollection 2021.
Bone mesenchymal stem cells (BMSCs) of multi-directional differentiation and reproductive activity are attractive candidates for bone and cartilage repair. However, the molecular mechanisms underlying the early phase of osteogenesis, adipogenesis, and chondrogenesis of BMSCs are still far from understood. In the current study, BMSCs are isolated from rats, and the gene expressions during the initiation of differentiation (phase I), lineage acquisition (phase II), and early lineage progression (phase III) of three-directional differentiation of BMSCs were detected by using high-throughput sequencing. Then, 356, 540, and 299 differentially expressed genes (DEGs) were identified in phases I, II, and III of osteogenesis, respectively. The numbers are 507, 287, and 428 for adipogenesis, respectively, and 412, 336, and 513 for chondrogenesis, respectively. Time-dependent expression patterns of genes were also validated during three-directional differentiation in BMSCs. Hub genes including , , and may act as common participants in initiating osteogenesis, adipogenesis, and chondrogenesis. , , and showed an enhanced expression throughout three early phases during the osteogenic differentiation but no significant change in other two-directional differentiation. A similar pattern of and expression occurred in adipogenesis and chondrogenesis, respectively. Our findings will help understand the underlying mechanism determining the differentiation fate of BMSCs and provide theoretical support for the clinical treatment of osteoporosis, osteoarthritis, and other age-related bone diseases.
具有多向分化和增殖活性的骨髓间充质干细胞(BMSCs)是骨和软骨修复的理想候选细胞。然而,BMSCs成骨、成脂和成软骨早期阶段的分子机制仍远未明确。在本研究中,从大鼠中分离出BMSCs,并通过高通量测序检测BMSCs三向分化起始阶段(I期)、谱系获得阶段(II期)和早期谱系进展阶段(III期)的基因表达。然后,在成骨的I期、II期和III期分别鉴定出356、540和299个差异表达基因(DEGs)。成脂的相应数字分别为507、287和428,成软骨的相应数字分别为412、336和513。基因的时间依赖性表达模式也在BMSCs的三向分化过程中得到验证。包括 、 和 在内的枢纽基因可能是启动成骨、成脂和成软骨的共同参与者。 在成骨分化的整个三个早期阶段表达增强,但在其他两个方向的分化中无显著变化。 和 在成脂和成软骨过程中分别出现类似的表达模式。我们的研究结果将有助于理解决定BMSCs分化命运的潜在机制,并为骨质疏松症、骨关节炎和其他与年龄相关的骨疾病的临床治疗提供理论支持。