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Regulation of matrix metalloproteinase-9 protein expression by 1α25-(OH)2D3 during osteoclast differentiation

机译:1α25-(OH)2D3在破骨细胞分化过程中对基质金属蛋白酶9蛋白表达的调控

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摘要

To investigate 1α,25-(OH)2D3 regulation of matrix metalloproteinase-9 (MMP-9) protein expression during osteoclast formation and differentiation, receptor activator of nuclear factor κB ligand (RANKL) and macrophage colony-stimulating factor (M-CSF) were administered to induce the differentiation of RAW264.7 cells into osteoclasts. The cells were incubated with different concentrations of 1α,25-(OH)2D3 during culturing, and cell proliferation was measured using the methylthiazol tetrazolium method. Osteoclast formation was confirmed using tartrate-resistant acid phosphatase (TRAP) staining and assessing bone lacunar resorption. MMP-9 protein expression levels were measured with Western blotting. We showed that 1α,25-(OH)2D3 inhibited RAW264.7 cell proliferation induced by RANKL and M-CSF, increased the numbers of TRAP-positive osteoclasts and their nuclei, enhanced osteoclast bone resorption, and promoted MMP-9 protein expression in a concentration-dependent manner. These findings indicate that 1α,25-(OH)2D3 administered at a physiological relevant concentration promoted osteoclast formation and could regulate osteoclast bone metabolism by increasing MMP-9 protein expression during osteoclast differentiation.
机译:研究破骨细胞形成和分化过程中基质金属蛋白酶9(MMP-9)蛋白表达的1α,25-(OH)2D3调节,核因子κB配体(RANKL)受体激活剂和巨噬细胞集落刺激因子(M-CSF)给药以诱导RAW264.7细胞分化为破骨细胞。在培养过程中,将细胞与不同浓度的1α,25-(OH)2D3孵育,并使用甲基噻唑四唑法测量细胞增殖。使用抗酒石酸酸性磷酸酶(TRAP)染色并评估骨腔隙吸收,确认破骨细胞形成。用蛋白质印迹法测量MMP-9蛋白表达水平。我们发现1α,25-(OH)2D3抑制RANKL和M-CSF诱导的RAW264.7细胞增殖,增加TRAP阳性破骨细胞及其核的数量,增强破骨细胞骨吸收,并促进MMP-9蛋白表达。浓度依赖性的方式。这些发现表明,以生理相关浓度施用的1α,25-(OH)2 D 3促进破骨细胞形成并且可以通过在破骨细胞分化过程中增加MMP-9蛋白表达来调节破骨细胞骨代谢。

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