Key result
Osteogenic medium increases RUNX2 expression ~88% in epicardial adipose-derived stem cells.
Why the study?
To assess the osteogenic potential of mesenchymal stem cells of epicardial adipose tissue in patients with stable coronary heart disease based on osteogenesis marker gene profiles.
Effect estimate: 1.88 times higher
p-value: p=0.012
Mesenchymal stem cells derived from the epicardial adipose tissue of patients with coronary heart disease demonstrate inherent osteogenic potential, suggesting they may act as preosteoblasts contributing to vascular calcification.
Epicardial MSC osteogenic potential in vitro warrants mechanistic studies on vascular calcification; leaves open any clinical role in coronary disease.
Aim . To assess the osteogenic potential of mesenchymal stem cells (MSCs) of epicardial adipose tissue (EAT) in patients with stable coronary heart disease based on obtaining gene profiles (osteogenesis markers). Materials and methods . In EAT MSCs, the expression levels of the RUNX2 (RUNX transcription factor encoding gene), BGLAP (osteocalcin encoding gene), SPP1 (osteopontin encoding gene), SP7 (Osterix encoding gene) genes were determined using real-time polymerase chain reaction (PCR). Using immunofluorescence staining, the amount of RUNX2, osteocalcin, osteopontin, and Osterix proteins was determined in the supernatant of cultured MSCs. Results . It was found that the expression of RUNX2 in cells cultured in a medium with osteoinducers was 1.88 times higher than in undifferentiated MSCs (p = 0.012). The level of RUNX2 protein was also higher in a differentiated cell culture (p < 0.05). Similar results were obtained regarding the level of SPP1 mRNA expression (p = 0.012). BGLAP expression did not differ between differentiated and undifferentiated MSC cultures. The level of SP7 gene expression did not differ in cells either with or without an osteoblastic medium. It is worth noting that using immunofluorescence staining, there were no differences detected in the expression of Osterix and OCN between cultures of differentiated and undifferentiated cells. Conclusion . It was found that EAT MSCs have osteogenic potential, which was manifested by the expression of osteogenesis genes in both differentiated and undifferentiated MSCs. The increase in the expression level of SSP1 and RUNX2 mRNA on the 15th day of cultivation with osteoblastic medium indicates that the studied cells are preosteoblasts and are at the stage of extracellular matrix synthesis.
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Учасова et al. (2025) studied Stable coronary heart disease (n=5). Osteogenic differentiation medium vs. Standard medium (undifferentiated MSCs) was evaluated on RUNX2 mRNA expression level (1.88 times higher, p=0.012). Culturing epicardial adipose tissue mesenchymal stem cells in an osteogenic medium increased RUNX2 gene expression by 1.88 times compared to undifferentiated cells (p=0.012).
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