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首页> 外文期刊>Journal of Veterinary Science >Regulation of matrix metalloproteinase-9 protein expression by 1α, 25-(OH)2D3 during osteoclast differentiation
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Regulation of matrix metalloproteinase-9 protein expression by 1α, 25-(OH)2D3 during osteoclast differentiation

机译:将基质金属蛋白酶-9蛋白表达的调节1α,25-(OH) 2 D 3 在破骨细胞分化期间

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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:探讨骨液醛形成和分化期间基质金属蛋白酶-9(MMP-9)蛋白表达的基质金属蛋白酶-9(MMP-9)蛋白表达的1α,25-(OH)<亚> D 调节,核因子的受体活化剂施用κB配体(RANKL)和巨噬细胞群刺激因子(M-CSF),诱导Raw264.7细胞分化成骨壳细胞。将细胞与不同浓度的1α,25-(OH)<亚> D D D 3孵育在培养过程中,使用甲基噻唑四唑鎓法测量细胞增殖。使用耐酒氨酸酸性磷酸酶(疏水阀)染色并评估骨凝集裂变术来证实骨核糖体形成。用蛋白质印迹测量MMP-9蛋白表达水平。我们展示了1α,25-(OH)<亚> 2 D 3 抑制RANKL和M-CSF诱导的RAW264.7细胞增殖,增加了捕集阳性骨质体的数量和它们的核,增强的骨壳骨吸收,并以浓度依赖性方式促进MMP-9蛋白表达。这些发现表明,以生理相关浓度施用的1α,25-(OH)<亚> 2 D 在生理相关浓度促进的破骨细胞形成,并且可以通过增加MMP-9蛋白表达来调节骨酸骨代谢在破骨细胞分化期间。

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