Synergistic effects of dexamethasone and vitamins D and K on mesenchymal stem cell differentiation.

IF 4.6 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Jana Dvorakova, Jana Kolaja Dobra, Lucie Hauer, Petra Kocanek Chocholata, Miroslava Cedikova, Anna Nekleionova, Vaclav Babuska
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引用次数: 0

Abstract

Background: The ability to guide stem cells toward the bone-forming lineage is a fundamental aspect of regenerative medicine. Conventional protocols for osteogenic differentiation of mesenchymal stem cells typically rely on continuous exposure to the synthetic steroid dexamethasone, in combination with other supplements such as ascorbate and glycerophosphate. Although dexamethasone effectively induces bone-related gene expression and matrix mineralization, prolonged or excessive exposure can lead to adverse catabolic and cytotoxic effects. Therefore, there is a need to develop improved culture conditions that retain efficacy while enhancing physiological relevance, safety, and reproducibility. This study investigated whether 1-week dexamethasone exposure and supplementing the medium with vitamin D3 and the synthetic vitamin K analogue K3 could enhance osteogenic differentiation of bone marrow-derived mesenchymal stem cells.

Methods: Stem cells were cultured for 28 days in four types of osteogenic media differing in the duration of dexamethasone exposure and the presence of vitamins D3 and K3. Osteogenic differentiation was evaluated using histochemical staining for mineralized matrix, quantification of calcium deposition, analysis of alkaline phosphatase activity, fluorescence microscopy of cellular morphology and mitochondrial organization, and gene expression of osteogenic markers including RUNX2, alkaline phosphatase, osteocalcin, and bone morphogenetic protein 2.

Results: A short exposure to dexamethasone alone was insufficient to support robust osteogenic progression, confirming the importance of sustained stimulation. In contrast, the combination of vitamins D3 and K3 produced a clear synergistic effect, characterized by stronger mineralization, increased alkaline phosphatase activity, and enhanced expression of key osteogenic genes.

Conclusions: This study demonstrates that the combined use of vitamins D3 and K3, together with optimized dexamethasone exposure, provides a simple and biologically compatible strategy to improve the osteogenic differentiation of mesenchymal stem cells. This approach offers a physiologically relevant, safe, and cost-effective modification of standard osteogenic protocols and may contribute to the development of more efficient cell-based systems for bone tissue engineering and regenerative medicine.

地塞米松与维生素D、K对间充质干细胞分化的协同作用。
背景:引导干细胞向骨形成谱系的能力是再生医学的一个基本方面。间充质干细胞成骨分化的传统方案通常依赖于连续暴露于合成类固醇地塞米松,并结合其他补充剂,如抗坏血酸盐和甘油磷酸盐。虽然地塞米松有效地诱导骨相关基因表达和基质矿化,但长期或过量暴露可导致不良的分解代谢和细胞毒性作用。因此,有必要开发改进的培养条件,在保持有效性的同时增强生理相关性、安全性和可重复性。本研究探讨了1周地塞米松暴露和补充维生素D3和合成维生素K类似物K3的培养基是否能增强骨髓源性间充质干细胞的成骨分化。方法:将干细胞在地塞米松暴露时间和维生素D3和K3含量不同的四种成骨培养基中培养28天。通过矿化基质的组织化学染色、钙沉积定量、碱性磷酸酶活性分析、细胞形态和线粒体组织的荧光显微镜、成骨标志物RUNX2、碱性磷酸酶、骨钙素和骨形态发生蛋白2的基因表达来评估成骨分化。结果:短期单独暴露于地塞米松不足以支持强大的成骨进展,证实了持续刺激的重要性。而维生素D3与K3联合使用具有明显的协同作用,矿化作用增强,碱性磷酸酶活性增加,关键成骨基因表达增强。结论:本研究表明,维生素D3和K3的联合使用,以及优化的地塞米松暴露,提供了一种简单且生物相容的策略来改善间充质干细胞的成骨分化。该方法为标准成骨方案提供了一种生理学上相关的、安全的、具有成本效益的修改,并可能有助于开发更有效的基于细胞的骨组织工程和再生医学系统。
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来源期刊
BioMedical Engineering OnLine
BioMedical Engineering OnLine 工程技术-工程:生物医学
CiteScore
6.70
自引率
2.60%
发文量
79
审稿时长
1 months
期刊介绍: BioMedical Engineering OnLine is an open access, peer-reviewed journal that is dedicated to publishing research in all areas of biomedical engineering. BioMedical Engineering OnLine is aimed at readers and authors throughout the world, with an interest in using tools of the physical and data sciences and techniques in engineering to understand and solve problems in the biological and medical sciences. Topical areas include, but are not limited to: Bioinformatics- Bioinstrumentation- Biomechanics- Biomedical Devices & Instrumentation- Biomedical Signal Processing- Healthcare Information Systems- Human Dynamics- Neural Engineering- Rehabilitation Engineering- Biomaterials- Biomedical Imaging & Image Processing- BioMEMS and On-Chip Devices- Bio-Micro/Nano Technologies- Biomolecular Engineering- Biosensors- Cardiovascular Systems Engineering- Cellular Engineering- Clinical Engineering- Computational Biology- Drug Delivery Technologies- Modeling Methodologies- Nanomaterials and Nanotechnology in Biomedicine- Respiratory Systems Engineering- Robotics in Medicine- Systems and Synthetic Biology- Systems Biology- Telemedicine/Smartphone Applications in Medicine- Therapeutic Systems, Devices and Technologies- Tissue Engineering
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