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Osteoclast precursors display dynamic metabolic shifts toward accelerated glucose metabolism at an early stage of RANKL-Stimulated osteoclast differentiation

机译:破骨细胞前体在RANKL刺激的破骨细胞分化的早期显示出动态的代谢向加速的葡萄糖代谢转变

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Mature osteoclasts have an increased citric acid cycle and mitochondrial respiration to generate high ATP production and ultimately lead to bone resorption. However, changes in metabolic pathways during osteoclast differentiation have not been fully illustrated. We report that glycolysis and oxidative phosphorylation characterized by glucose and oxygen consumption as well as lactate production were increased during receptor activator of nuclear factor-kappa B ligand (RANKL)-induced osteoclastogenesis from RAW264.7 and bone marrow-derived macrophage cells. Cell proliferation and differentiation varied according to glucose concentrations (0 to 100 mM). Maximal cell growth occurred at 20 mM glucose concentration and differentiation occurred at 5 mM concentration. Despite the similar growth rates exhibited when cultured cells were exposed to either 5 mM or 40 mM glucose, their differentiation was markedly decreased in high glucose concentrations. This finding suggests the possibility that osteoclastogenesis could be regulated by changes in metabolic substrate concentrations. To further address the effect of metabolic shift on osteoclastogenesis, we exposed cultured cells to pyruvate, which is capable of promoting mitochondrial respiration. Treatment of pyruvate synergistically increased osteoclastogenesis through the activation of RANKL-stimulated signals (ERK and JNK). We also found that osteoclastogenesis was retarded by blocking ATP production with either the inhibitors of mitochondrial complexes, such as rotenone and antimycin A, or the inhibitor of ATP synthase, oligomycin. Taken together, these results indicate that glucose metabolism during osteoclast differentiation is accelerated and that a metabolic shift towards mitochondrial respiration allows high ATP production and induces enhanced osteoclast differentiation. Copyright (c) 2007 S. Karger AG, Basel.
机译:成熟的破骨细胞具有增加的柠檬酸循环和线粒体呼吸,从而产生高的ATP产生量并最终导致骨吸收。但是,破骨细胞分化过程中代谢途径的变化尚未完全阐明。我们报告的糖酵解和氧化磷酸化为特征的葡萄糖和氧气消耗以及乳酸的产生在从RAW264.7和骨髓源性巨噬细胞的核因子-κB配体(RANKL)诱导的破骨细胞的受体激活剂中增加。细胞增殖和分化随葡萄糖浓度(0至100 mM)而变化。在20 mM葡萄糖浓度下最大细胞生长发生,在5 mM浓度下发生分化。尽管将培养的细胞暴露于5 mM或40 mM葡萄糖时显示出相似的生长速率,但在高葡萄糖浓度下它们的分化明显降低。这一发现表明破骨细胞生成可能受代谢底物浓度变化的调节。为了进一步解决代谢转变对破骨细胞生成的影响,我们将培养的细胞暴露于丙酮酸中,丙酮酸能够促进线粒体呼吸。丙酮酸的治疗通过激活RANKL刺激的信号(ERK和JNK)来协同增加破骨细胞的生成。我们还发现,通过用线粒体复合物的抑制剂(如鱼藤酮和抗霉素A)或ATP合酶的抑制剂(寡霉素)阻断ATP的产生,破骨细胞的生成受到了阻碍。综上所述,这些结果表明破骨细胞分化期间的葡萄糖代谢被加速,并且向线粒体呼吸的代谢转变允许高ATP产生并诱导破骨细胞分化增强。版权所有(c)2007 S.Karger AG,巴塞尔。

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