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首页> 外文期刊>Archives of Toxicology >Sodium fluoride suppress proliferation and induce apoptosis through decreased insulin-like growth factor-I expression and oxidative stress in primary cultured mouse osteoblasts
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Sodium fluoride suppress proliferation and induce apoptosis through decreased insulin-like growth factor-I expression and oxidative stress in primary cultured mouse osteoblasts

机译:氟化钠可抑制胰岛素样生长因子-I表达和氧化应激,从而抑制增殖并诱导凋亡。

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It has been reported that sodium fluoride suppressed proliferation and induced apoptosis in osteoblasts. However, the details about the mechanism at work in bone metabolism are limited. In this study, we further investigated the mechanisms of NaF on proliferation and apoptosis in the primary cultured mouse osteoblasts, which were exposed to different concentration of NaF (10−6–5 × 10−4 M). We examined the effect of NaF on proliferation, cell cycle, apoptosis, oxidative stress, and the protein level of insulin-like growth factor-I (IGF-I) in osteoblasts. All the tested NaF inhibited proliferation and arrested cell cycle at S phase in osteoblasts, and further demonstrated to induce apoptosis in osteoblasts. On the other hand, we found that NaF increased oxidative stress and decreased protein expression of IGF-I. Our study herein suggested that NaF caused proliferation suppression, and apoptosis may contribute to decrease IGF-I expression and increased oxidative stress damage by NaF in the primary mouse osteoblasts.
机译:据报道,氟化钠抑制成骨细胞的增殖并诱导凋亡。但是,有关骨代谢机制的细节有限。在这项研究中,我们进一步研究了NaF对原代培养的成骨细胞的增殖和凋亡的机制,成骨细胞暴露于不同浓度的NaF(10 −6 –5×10 −4 M)。我们检查了NaF对成骨细胞中增殖,细胞周期,凋亡,氧化应激和胰岛素样生长因子-I(IGF-I)蛋白质水平的影响。所有测试的NaF都抑制成骨细胞在S期增殖并阻止其细胞周期,并进一步证明可诱导成骨细胞凋亡。另一方面,我们发现NaF增加了氧化应激并且降低了IGF-I的蛋白质表达。我们在此的研究表明,NaF引起增殖抑制,而凋亡可能导致NaF在原代小鼠成骨细胞中降低IGF-I表达并增加氧化应激损伤。

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