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Ce 对 MC3T3-E1 细胞体外增殖、成骨分化及矿化功能的影响。

The effects of Ce on the proliferation, osteogenic differentiation and mineralization function of MC3T3-E1 cells in vitro.

机构信息

College of Chemistry and Environmental Science, Chemical Biology Key Laboratory of Hebei Province, Hebei University, Baoding, People's Republic of China.

出版信息

Biol Trace Elem Res. 2012 Nov;149(2):291-7. doi: 10.1007/s12011-012-9423-8. Epub 2012 Apr 25.

Abstract

The effects of Ce on the proliferation, osteogenic differentiation and mineralization function of a murine preosteoblast cell line MC3T3-E1 in vitro were investigated at cell and molecular levels. The results showed that Ce promoted the proliferation, osteogenic differentiation and mineralization function of MC3T3-E1 cells at concentrations of 0.0001, 0.001, 0.01, 0.1 and 1 μM, but turned to inhibit the proliferation, osteogenic differentiation and mineralization function at concentrations of 10, 100 and 1000 μM. Ce displayed the up-regulation of Runx2, BMP2, ALP, BSP, Col I and OCN genes at concentrations of 0.0001 and 0.1 μM; these genes were down-regulated in the MC3T3-E1 cells treated with 1000 μM Ce. The expression of BMP2, Runx2 and OCN proteins was promoted by Ce at concentrations of 0.0001 and 0.1 μM, but these proteins were down-regulated after 1000 μM Ce treatment. The results suggest that Ce likely up-regulates or down-regulates the expression of Runx2, which subsequently up- or down-regulates OB marker genes Col I and BMP2 at early stages and ALP and OCN at later stages of differentiation, thus causing to promote or inhibit the proliferation, osteogenic differentiation and mineralization function of MC3T3-E1 cells.

摘要

研究了 Ce 对体外鼠前成骨细胞系 MC3T3-E1 细胞增殖、成骨分化和矿化功能的影响,在细胞和分子水平上。结果表明,Ce 在 0.0001、0.001、0.01、0.1 和 1 μM 浓度下促进 MC3T3-E1 细胞的增殖、成骨分化和矿化功能,但在 10、100 和 1000 μM 浓度下则抑制其增殖、成骨分化和矿化功能。Ce 在 0.0001 和 0.1 μM 浓度下上调 Runx2、BMP2、ALP、BSP、Col I 和 OCN 基因;在 1000 μM Ce 处理的 MC3T3-E1 细胞中,这些基因下调。Ce 在 0.0001 和 0.1 μM 浓度下促进 BMP2、Runx2 和 OCN 蛋白的表达,但在 1000 μM Ce 处理后,这些蛋白下调。结果表明,Ce 可能上调或下调 Runx2 的表达,进而在分化的早期上调或下调 OB 标志物基因 Col I 和 BMP2,在后期上调或下调 ALP 和 OCN,从而促进或抑制 MC3T3-E1 细胞的增殖、成骨分化和矿化功能。

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