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Combined effects of simvastatin and fibroblast growth factor-2 on the proliferation and differentiation of preosteoblasts

机译:辛伐他汀和成纤维细胞生长因子-2联合作用对成骨细胞增殖和分化的影响

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摘要

Simvastatin reportedly promotes osteoblastic and inhibits osteoclastic activity. It increases bone formation when injected subcutaneously over the calvaria in mice. It also increases cancellous bone volume in rats following oral administration. Fibroblast growth factor-2 (FGF-2), a member of the FGF family, is expressed by cells of the osteoblastic lineage. FGF-2 promotes osteoblast proliferation and it is secreted during the healing process of fractures or at bone surgery sites. FGF-2 reportedly regulates bone formation and osteoblast differentiation. In this study, the combined effects of simvastatin and FGF-2 on the proliferation and differentiation of preosteoblasts were investigated and an alkaline phosphatase (ALP) activity test was performed to assess the differentiation. Moreover, the expression of proteins associated with bone formation were measured using western blot analysis. The results demonstrated that the protein content of the cultures grown in osteogenic differentiation media in the presence of FGF-2 at a concentration of 20 ng/ml was higher compared to that of the untreated control cultures. ALP activity was decreased when cells were treated with FGF-2 (2 and 20 ng/ml) and increased when cells were treated with simvastatin. The cultures grown in the presence of 1 μM of simvastatin and 2 ng/ml of FGF-2 exhibited increased ALP activity when compared to that in the 2 ng/ml FGF-2-only group. The combination of 1.0 μM simvastatin and 2 ng/ml FGF-2 achieved a higher estrogen receptor-α expression compared to the 2 ng/ml FGF-2-only group. Within the limits of this study, simvastatin enhanced osteoblast differentiation. However, the combined treatment with simvastatin and FGF-2 did not exert synergistic effects on osteoblast differentiation under the current experimental conditions. Future studies are required to evaluate divergent conditions and determine the selective timing and optimal dosage for the delivery of the agents.
机译:据报道,辛伐他汀促进成骨细胞并抑制破骨细胞活性。当在小鼠的颅底皮下注射时,它会增加骨形成。口服后,它还会增加大鼠的松质骨体积。成纤维细胞生长因子-2(FGF-2)是FGF家族的成员,由成骨细胞谱系的细胞表达。 FGF-2促进成骨细胞增殖,并在骨折愈合过程中或在骨外科手术部位分泌。据报道,FGF-2调节骨形成和成骨细胞分化。在这项研究中,研究了辛伐他汀和FGF-2对成骨细胞增殖和分化的联合作用,并进行了碱性磷酸酶(ALP)活性测试以评估其分化。此外,使用蛋白质印迹分析测量与骨形成相关的蛋白质的表达。结果表明,与未处理的对照培养物相比,在FGF-2存在下在成骨分化培养基中生长的培养物的蛋白质含量更高,浓度为20 ng / ml。当用FGF-2(2和20 ng / ml)处理细胞时,ALP活性降低;当用辛伐他汀处理细胞时,ALP活性升高。与仅2 ng / ml FGF-2组相比,在1μM辛伐他汀和2 ng / ml FGF-2存在下生长的培养物显示出增加的ALP活性。与仅2 ng / ml FGF-2的组相比,1.0μM辛伐他汀和2 ng / ml FGF-2的组合获得了更高的雌激素受体-α表达。在这项研究的范围内,辛伐他汀可增强成骨细胞的分化。然而,在当前的实验条件下,辛伐他汀和FGF-2的联合治疗对成骨细胞的分化没有协同作用。需要进一步的研究来评估不同的条件,并确定药物递送的选择性时机和最佳剂量。

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