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Adenosine Triphosphate stimulates differentiation and mineralization in human osteoblast-like Saos-2 cells

机译:三磷酸腺苷刺激人成骨细胞样Saos-2细胞的分化和矿化

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摘要

In the last years adenosine triphosphate (ATP) and subsequent purinergic system activation through P2 receptors were investigated highlighting their pivotal role in bone tissue biology. In osteoblasts ATP can regulate several activities like cell proliferation, cell death, cell differentiation and matrix mineralization. Since controversial results exist, in this study we analyzed the ATP effects on differentiation and mineralization in human osteoblast-like Saos-2 cells. We showed for the first time the altered functional activity of ATP receptors. Despite that, we found that ATP can reduce cell proliferation and stimulate osteogenic differentiation mainly in the early stages of invitro maturation as evidenced by the enhanced expression of alkaline phosphatase (ALP), Runt-related transcription factor 2 (Runx2) and Osteocalcin (OC) genes and by the increased ALP activity. Moreover, we found that ATP can affect mineralization in a biphasic manner, at low concentrations ATP always increases mineral deposition while at high concentrations it always reduces mineral deposition. In conclusion, we show the osteogenic effect of ATP on both early and late stage activities like differentiation and mineralization, for the first time in human osteoblastic cells.
机译:近年来,对三磷酸腺苷(ATP)及其随后的嘌呤能系统通过P2受体的活化进行了研究,突出了它们在骨组织生物学中的关键作用。在成骨细胞中,ATP可以调节多种活性,例如细胞增殖,细胞死亡,细胞分化和基质矿化。由于存在有争议的结果,因此在这项研究中,我们分析了ATP对人成骨细胞样Saos-2细胞分化和矿化的影响。我们首次展示了ATP受体功能活性的改变。尽管如此,我们发现ATP仍可在体外成熟的早期阶段减少细胞增殖并刺激成骨细胞分化,碱性磷酸酶(ALP),矮子相关转录因子2(Runx2)和骨钙素(OC)的表达增强证明了这一点。基因和通过增加ALP活性。此外,我们发现ATP可以以两相方式影响矿化,在低浓度下ATP总是会增加矿物质的沉积,而在高浓度下ATP总是会减少矿物质的沉积。总之,我们首次显示了ATP对人成骨细胞中早期和晚期活动(如分化和矿化)的成骨作用。

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