Liang Zhaoquan, Wu Yuelin, Bao Junhao, Xiao Qiang, Luo Sidong, Liu Xinfang, Wang Yeyang, Xie Chao, Zhang Li
Department of Spine, Orthopaedic Center, Guangdong Second Provincial General Hospital, Southern Medical University, Guangzhou, China.
Department of Joint and Orthopedics, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
J Cell Mol Med. 2025 Jan;29(1):e70353. doi: 10.1111/jcmm.70353.
Osteogenic differentiation of bone marrow stem cells (BMSCs) is essential for bone tissue regeneration and repair. However, this process is often hindered by an unstable differentiation influenced by local microenvironmental factors. While small extracellular vesicles (sEVs) derived from osteogenically induced adipose mesenchymal stem cells (ADSCs) reportedly can promote osteogenic differentiation of BMSCs, the underlying molecular mechanisms remain incompletely understood. In this study, we investigated the mRNA expression profile of ADSC-sEVs and explored the role of specific mRNAs in the osteogenic differentiation of BMSCs. We first validated the osteogenic induction activity of ADSC-sEVs through both in vitro and in vivo experiments. Using reverse transcription polymerase chain reaction, we compared mRNA expression between ADSC-sEVs and ADSC-sEVs and further assessed the impact of specific mRNAs on the differentiation of BMSCs through a series of in vitro experiments. One of our key findings was that osterix mRNA was highly enriched in ADSC-sEVs, which significantly enhanced alkaline phosphatase staining and upregulated downstream osteoblastic markers in BMSCs. Both overexpression and knockdown experiments confirmed that osterix mRNA is a critical signalling molecule that facilitates the differentiation of BMSCs into osteoblasts through ADSC-sEVs. This finding expands our understanding of the molecular mechanisms underlying the osteogenic differentiation of BMSCs and offers a promising strategy for targeted osteoblastic differentiation in clinical applications.
骨髓干细胞(BMSCs)的成骨分化对于骨组织的再生和修复至关重要。然而,这一过程常常受到局部微环境因素影响而导致分化不稳定。据报道,源自成骨诱导脂肪间充质干细胞(ADSCs)的小细胞外囊泡(sEVs)能够促进BMSCs的成骨分化,但其潜在分子机制仍未完全明确。在本研究中,我们调查了ADSC-sEVs的mRNA表达谱,并探讨了特定mRNA在BMSCs成骨分化中的作用。我们首先通过体外和体内实验验证了ADSC-sEVs的成骨诱导活性。利用逆转录聚合酶链反应,我们比较了ADSC-sEVs之间的mRNA表达,并通过一系列体外实验进一步评估了特定mRNA对BMSCs分化的影响。我们的一项关键发现是,osterix mRNA在ADSC-sEVs中高度富集,其显著增强了碱性磷酸酶染色,并上调了BMSCs中下游成骨细胞标志物。过表达和敲低实验均证实,osterix mRNA是一种关键信号分子,可通过ADSC-sEVs促进BMSCs向成骨细胞分化。这一发现扩展了我们对BMSCs成骨分化潜在分子机制的理解,并为临床应用中靶向成骨细胞分化提供了一种有前景的策略。