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Metabolomic Analysis Reveals Vitamin D-induced Decrease in Polyol Pathway and Subtle Modulation of Glycolysis in HEK293T Cells

机译:代谢组学分析揭示了维生素D诱导的多元醇途径减少和HEK293T细胞糖酵解的微调。

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摘要

We combined 1H NMR metabolomics with functional and molecular biochemical assays to describe the metabolic changes elicited by vitamin D in HEK293T, an embryonic proliferative cell line adapted to high-glucose concentrations. Activation of the polyol pathway, was the most important consequence of cell exposure to high glucose concentration, resembling cells exposed to hyperglycemia. Vitamin D induced alterations in HEK293T cells metabolism, including a decrease in sorbitol, glycine, glutamate, guanine. Vitamin D modulated glycolysis by increasing phosphoglycerate mutase and decreasing enolase activities, changing carbon fate without changing glucose consumption, lactate export and Krebs cycle. The decrease in sorbitol intracellular concentration seems to be related to vitamin D regulated redox homeostasis and protection against oxidative stress, and helped maintaining the high proliferative phenotype, supported by the decrease in glycine and guanine and orotate concentration and increase in choline and phosphocholine concentration. The decrease in orotate and guanine indicated an increased biosynthesis of purine and pyrimidines. Vitamin D elicited metabolic alteration without changing cellular proliferation and mitochondrial respiration, but reclaiming reductive power. Our study may contribute to the understanding of the metabolic mechanism of vitamin D upon exposure to hyperglycemia, suggesting a role of protection against oxidative stress.
机译:我们将 1 H NMR代谢组学与功能和分子生化分析相结合,描述了维生素D在HEK293T中引起的代谢变化,HEK293T是适应高葡萄糖浓度的胚胎增殖细胞系。多元醇途径的激活是细胞暴露于高葡萄糖浓度的最重要结果,类似于细胞暴露于高血糖症。维生素D诱导HEK293T细胞代谢的改变,包括山梨糖醇,甘氨酸,谷氨酸,鸟嘌呤的减少。维生素D通过增加磷酸甘油酸变位酶和减少烯醇酶活性,改变碳的命运而不改变葡萄糖的消耗,乳酸的输出和克雷布斯循环来调节糖酵解。山梨糖醇细胞内浓度的降低似乎与维生素D调节的氧化还原稳态和对氧化应激的保护有关,并有助于维持高增殖表型,甘氨酸和鸟嘌呤和乳清酸盐浓度的降低以及胆碱和磷酸胆碱浓度的提高也有助于维持这种状态。乳清酸盐和鸟嘌呤的减少表明嘌呤和嘧啶的生物合成增加。维生素D引起代谢改变,而没有改变细胞增殖和线粒体呼吸,但恢复了还原力。我们的研究可能有助于了解维生素D暴露于高血糖症后的代谢机制,这表明了对氧化应激的保护作用。

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