Zuvairiya Ummu, R Priyadharshini, Palati Sinduja
Department of General Pathology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, IND.
Department of Oral and Maxillofacial Pathology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, IND.
Cureus. 2024 May 14;16(5):e60292. doi: 10.7759/cureus.60292. eCollection 2024 May.
Introduction Maintaining bone health is crucial for overall well-being, with osteoblasts playing a vital role in bone formation. Bone morphogenetic protein-2 (BMP2) is a key regulator, stimulating bone matrix synthesis and osteoblast differentiation. Recognizing BMP2's significance, there's growing interest in natural compounds, such as . This study explores potential influence on BMP2 mRNA expression in osteoblast cells for insights into bone health modulation. Materials and methods This research utilized to explore its impact on MG-63 cells, a human osteoblast cell line. Osteoblast cells were cultured in Dulbecco's modified Eagle's medium (DMEM), supplemented with 10% heat-inactivated fetal bovine serum, and maintained at 37°C in a 5% CO2 and 95% air environment. Cell viability was evaluated by seeding osteoblast cells into 96-well plates and exposing them to different concentrations of (2.0 μg/ml and 20 μg/ml). The study observed both the promotion of osteoblast cell growth in MG-63 and morphological changes in the cells under an inverted light microscope at 10x magnification. Results were presented using one-way analysis of variance (ANOVA) conducted with IBM SPSS Statistics for Windows, Version 23 (Released 2015; IBM Corp., Armonk, New York, United States). Result The reverse transcription-polymerase chain (RT-PCR) results revealed an increased expression of BMP-2 mRNA fold change in comparison to the control group. A clear positive correlation was observed between the BMP-2 mRNA fold change and the notable increase in the concentration of . This investigation revealed a direct association of BMP-2 mRNA expression with the proliferation of osteoblast cells. Specifically, the BMP-2 mRNA fold change was recorded at 2.26±1.05 in at 2.0 μg/ml and 2.0 ± 0.84 at 20 μg/ml, with corresponding significances of 0.00, respectively. Conclusion Potential effects of on BMP-2 mRNA expression in osteoblast cells and its role in bone health modulation revealed that may upregulate BMP-2 mRNA expression, suggesting its potential as a natural compound for enhancing bone formation. The observed positive correlation between concentration and BMP-2 mRNA fold change showed the significance of this botanical agent in promoting osteoblast cell proliferation. These results highlight the importance of further research to explore the applications of in managing bone disorders and improving overall bone health.
引言 维持骨骼健康对整体健康至关重要,成骨细胞在骨形成中起着关键作用。骨形态发生蛋白-2(BMP2)是一种关键调节因子,可刺激骨基质合成和成骨细胞分化。鉴于BMP2的重要性,人们对天然化合物等的兴趣与日俱增。本研究探讨其对成骨细胞中BMP2 mRNA表达的潜在影响,以深入了解骨骼健康调节机制。材料与方法 本研究利用 [具体物质未提及] 来探究其对人成骨细胞系MG-63细胞的影响。成骨细胞在添加10%热灭活胎牛血清的杜尔贝科改良 Eagle 培养基(DMEM)中培养,并在37°C、5% CO2和95%空气环境中维持培养。通过将成骨细胞接种到96孔板中并使其暴露于不同浓度的 [具体物质未提及](2.0 μg/ml和20 μg/ml)来评估细胞活力。在倒置显微镜下以10倍放大倍数观察MG-63中成骨细胞的生长促进情况以及细胞形态变化。使用IBM SPSS Statistics for Windows 23版(2015年发布;IBM公司,美国纽约州阿蒙克)进行单因素方差分析(ANOVA)来呈现结果。结果 逆转录-聚合酶链反应(RT-PCR)结果显示,与对照组相比,BMP-2 mRNA的表达倍数变化增加。观察到BMP-2 mRNA倍数变化与 [具体物质未提及] 浓度的显著增加之间存在明显的正相关。本研究揭示了BMP-2 mRNA表达与成骨细胞增殖之间的直接关联。具体而言,在2.0 μg/ml的 [具体物质未提及] 中,BMP-2 mRNA倍数变化记录为2.26±1.05,在20 μg/ml时为2.0±0.84,相应的显著性分别为0.00。结论 [具体物质未提及] 对成骨细胞中BMP-2 mRNA表达的潜在影响及其在骨骼健康调节中的作用表明,[具体物质未提及] 可能上调BMP-2 mRNA表达,表明其作为促进骨形成的天然化合物的潜力。观察到的 [具体物质未提及] 浓度与BMP-2 mRNA倍数变化之间的正相关表明这种植物制剂在促进成骨细胞增殖方面的重要性。这些结果突出了进一步研究以探索 [具体物质未提及] 在管理骨疾病和改善整体骨骼健康方面应用的重要性。