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首页> 外文期刊>Journal of Experimental and Integrative Medicine >Effect of methylglyoxal on osteoprotegerin expression in the pre-osteoblast MC3T3E1 cell line: involvement of oxidant pathways
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Effect of methylglyoxal on osteoprotegerin expression in the pre-osteoblast MC3T3E1 cell line: involvement of oxidant pathways

机译:甲基乙二醛对成骨细胞前MC3T3E1细胞系中骨保护素表达的影响:氧化剂途径的参与

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Objective: This study aimed to evaluate osteoprotegerin (OPG) expression in MC3T3E1 preosteoblast cell line exposed to methylgyoxal (MG) with/without antioxidant blocking or iron chelating. Methods: MC3T3E1 preosteoblast cell line subclone 4 was obtained from American Type Culture Cell Collection (ATCC). Modulation of intracellular oxidative status was obtained by blockade of superoxide dismutase (SOD) using diethylthiocarbamoic acid (DETCA), blockade of gluthatione peroxidase (GPx) using mercaptosuccinate (MS), and iron chelating using deferoxamine (DFX). The MC3T3E1 preosteoblast cell line was exposed to MG at the concentration of 5 μM for 6 h of incubation time. Eight groups (n=3) were constituted, including the control group, the MG-exposed group, the DETCA/MS/DFX-exposed groups, and the MG+DETCA/MS/DFX-exposed groups. OPG was evaluated by ELISA assay kit. Results: The expression of OPG in MG-exposed group was not different than that in the control group. OPG expression was significantly reduced by DETCA and restored in the MG+DETCA-exposed group. MS exposure also significantly reduced OPG expression; addition of MG to MS again clearly reversed this effect. On the other hand, DFX administration did not affect OPG expression. Conclusion: Modulation of the intracelllular oxidative status via blockade of SOD or GPx clearly inhibits the OPG expression in preosteoblast cells. Addition of MG reversed this effect and reversed the fall of OPG expression.
机译:目的:本研究旨在评估在有/没有抗氧化剂阻断或铁螯合的情况下,暴露于甲基乙二醛(MG)的MC3T3E1前成骨细胞系中骨保护素(OPG)的表达。方法:MC3T3E1前成骨细胞系亚克隆4获自美国典型培养物保藏中心(ATCC)。通过使用二乙基硫代氨基甲酸(DETCA)阻止超氧化物歧化酶(SOD),使用巯基琥珀酸酯(MS)阻止谷胱甘肽过氧化物酶(GPx)和使用去铁胺(DFX)进行铁螯合来调节细胞内氧化状态。将MC3T3E1前成骨细胞细胞系以5μM的浓度暴露于MG中孵育6小时。组成八个组(n = 3),包括对照组,暴露于MG的组,暴露于DETCA / MS / DFX的组和暴露于MG + DETCA / MS / DFX的组。通过ELISA测定试剂盒评估OPG。结果:MG暴露组OPG的表达与对照组无差异。 OPG表达被DETCA显着降低,并在MG + DETCA暴露组中恢复。 MS暴露也显着降低OPG表达;将MG加入MS再一次明显逆转了这种效应。另一方面,DFX管理不影响OPG表达。结论:通过阻止SOD或GPx调节细胞内氧化状态,明显抑制了成骨细胞中OPG的表达。 MG的添加逆转了这种作用并且逆转了OPG表达的下降。

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