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首页> 外文期刊>The Journal of Nutritional Biochemistry >Nitric oxide mediates low magnesium inhibition of osteoblast-like cell proliferation
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Nitric oxide mediates low magnesium inhibition of osteoblast-like cell proliferation

机译:一氧化氮介导低镁抑制成骨样细胞增殖

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An adequate intake of magnesium (Mg) is important for bone cell activity and contributes to the prevention of osteoporosis. Because (a) Mg is mitogenic for osteoblasts and (b) reduction of osteoblast proliferation is detected in osteoporosis, we investigated the influence of different concentrations of extracellular Mg on osteoblast-like SaOS-2 cell behavior. We found that low Mg inhibited SaOS-2 cell proliferation by increasing the release of nitric oxide through the up-regulation of inducible nitric oxide synthase (iNOS). Indeed, both pharmacological inhibition with the iNOS inhibitor L-N6-(iminoethyl)-lysine-HCl and genetic silencing of iNOS by small interfering RNA restored the normal proliferation rate of the cells. Because a moderate induction of nitric oxide is sufficient to potentiate bone resorption and a relative deficiency in osteoblast proliferation can result in their inadequate activity, we conclude that maintaining Mg homeostasis is relevant to ensure osteoblast function and, therefore, to prevent osteoporosis.
机译:充足的镁(Mg)摄入对于骨细胞的活动很重要,并有助于预防骨质疏松症。因为(a)Mg对成骨细胞有丝分裂作用,并且(b)在骨质疏松症中检测到成骨细胞增殖减少,所以我们研究了不同浓度的细胞外Mg对成骨细胞样SaOS-2细胞行为的影响。我们发现低镁通过上调诱导型一氧化氮合酶(iNOS)来增加一氧化氮的释放,从而抑制了SaOS-2细胞的增殖。确实,iNOS抑制剂L-N 6 -(亚氨基乙基)-赖氨酸-HCl的药理抑制作用和小干扰RNA对iNOS的基因沉默均可恢复细胞的正常增殖率。由于适度诱导一氧化氮足以增强骨吸收,并且成骨细胞增殖相对不足会导致其活性不足,因此我们得出结论,维持镁稳态对确保成骨细胞功能至关重要,因此可以预防骨质疏松。

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