Ding Mina, Hu Zhiwei, Pei Ke, Hu Junyuan, Liao Yan, Cai Cheguo, Zhang Jian V
Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Shenzhen Key Laboratory of Metabolic Health, Shenzhen Metabolism and Reproductive Targeted Delivery Proof-of-Concept Center, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
Calcif Tissue Int. 2025 Jul 18;116(1):100. doi: 10.1007/s00223-025-01407-4.
The balance between adipogenesis and osteogenesis in mesenchymal stem cells (MSCs) is pivotal for the maintenance of bone homeostasis. However, the genes responsible for regulating this balance are still not fully understood. This investigation sought to explore and identify novel genes that influence MSC differentiation into adipogenic and osteogenic lineages, thereby enhancing bone formation. Four datasets from the Gene Expression Omnibus (GEO) database were utilized: three focused on osteogenic differentiation (GSE73087, GSE18043, GSE114117), and one on adipogenic differentiation (GSE37836). Differentially expressed genes (DEGs) during both osteogenic and adipogenic differentiation processes were analyzed using the limma R package. A sum of 471 common differentially expressed genes (CDEGs) were found in MSC osteogenesis, comprising 240 elevated and 231 reduced genes. Similarly, in MSCs adipogenesis, 204 elevated genes and 459 reduced genes were identified. Fourteen hub genes were found to overlap between the CDEGs associated with MSC osteogenesis and DEGs linked to adipogenic differentiation. Notably, the expression of aryl hydrocarbon receptor nuclear translocator 2 (ARNT2) was elevated during osteogenesis but reduced during adipogenesis. Overexpression of ARNT2 enhanced the expression of osteogenic markers in MSCs, while its suppression led to a decrease in osteogenic marker expression. Protein-protein interaction network analysis revealed that ARNT2 interacts with Hypoxia inducible factor 1 subunit alpha (HIF1A), B-cell lymphoma 6 (BCL6), Ubiquitin-specific-processing protease 7 (USP7), and Single-minded homolog 2 (SIM2), which are implicated in the regulation of MSCs osteogenesis. In summary, fourteen hub genes were identified as potential regulators in the osteo-adipogenic differentiation of MSCs. Among them, ARNT2 was confirmed to promote osteogenesis in MSCs and exhibited potential as a therapeutic target for bone-related diseases.
间充质干细胞(MSCs)中脂肪生成与成骨之间的平衡对于维持骨稳态至关重要。然而,负责调节这种平衡的基因仍未完全明确。本研究旨在探索并鉴定影响MSCs向脂肪生成和成骨谱系分化的新基因,从而促进骨形成。利用了基因表达综合数据库(GEO)中的四个数据集:三个聚焦于成骨分化(GSE73087、GSE18043、GSE114117),一个聚焦于脂肪生成分化(GSE37836)。使用limma R包分析了成骨和脂肪生成分化过程中的差异表达基因(DEGs)。在MSCs成骨过程中发现了471个共同差异表达基因(CDEGs),包括240个上调基因和231个下调基因。同样,在MSCs脂肪生成过程中,鉴定出204个上调基因和459个下调基因。发现14个枢纽基因在与MSCs成骨相关的CDEGs和与脂肪生成分化相关的DEGs之间重叠。值得注意的是,芳烃受体核转运蛋白2(ARNT2)的表达在成骨过程中升高,但在脂肪生成过程中降低。ARNT2的过表达增强了MSCs中成骨标志物的表达,而其抑制导致成骨标志物表达下降。蛋白质-蛋白质相互作用网络分析表明,ARNT2与缺氧诱导因子1α亚基(HIF1A)、B细胞淋巴瘤6(BCL6)、泛素特异性加工蛋白酶7(USP7)和单 minded同源物2(SIM2)相互作用,这些因子参与MSCs成骨的调节。总之,14个枢纽基因被鉴定为MSCs骨-脂肪生成分化的潜在调节因子。其中,ARNT2被证实可促进MSCs的成骨作用,并展现出作为骨相关疾病治疗靶点的潜力。
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