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    陆静, 邓旭, 顾正清. LC-MS代谢组学研究高糖对NRK-52E细胞的损伤机制[J]. 徐州医科大学学报, 2018, 38(10): 659-663.
    引用本文: 陆静, 邓旭, 顾正清. LC-MS代谢组学研究高糖对NRK-52E细胞的损伤机制[J]. 徐州医科大学学报, 2018, 38(10): 659-663.
    Study on the mechanism of NRK-52E cell injured by high glucose using LC-MS metabolomics[J]. Journal of Xuzhou Medical University, 2018, 38(10): 659-663.
    Citation: Study on the mechanism of NRK-52E cell injured by high glucose using LC-MS metabolomics[J]. Journal of Xuzhou Medical University, 2018, 38(10): 659-663.

    LC-MS代谢组学研究高糖对NRK-52E细胞的损伤机制

    Study on the mechanism of NRK-52E cell injured by high glucose using LC-MS metabolomics

    • 摘要: 目的 通过液相色谱-质谱联用(LC-MS)代谢组学技术分析高糖干预后细胞内代谢物改变,来评价高糖对大鼠肾小管上皮细胞(NRK-52E)的潜在损伤机制。方法 NRK-52E细胞经常规培养方法培养12 h后,随机分为低糖组(LG组,5.56 mmol/L,n=6)和高糖组(HG组,25 mmol/L,n=6),继续培养48 h,采用LC-MS检测细胞内所含代谢物,利用Mass Profile Professional(MPP)软件进行主成分分析(Principal component analysis, PCA)和偏最小二乘判别分析(Partial least squares to latent structure-discriminant analysis, PLS-DA)寻找差异代谢物。结果 高糖显著损伤细胞形态。细胞代谢物中共鉴定出亮氨酸、神经酰胺(d18:0/12:0, d20:0/16:0, d18:0/16:0, t18:0/16:0, d18:0/14:0)、磷脂酰丝氨酸(16:0/16:0, 14:0/12:0, 20:0/0:0)、次黄嘌呤、磷脂酰肌醇(17:2/20:2)、溶血磷脂酰乙醇胺(0:0/20:5, 0:0/20:2)、磷脂酰乙醇胺(16:0/0:0)等15种差异性代谢物。结论 高糖对NRK-52E细胞的损伤与细胞内氨基酸、嘌呤、磷脂等代谢密切相关。

       

      Abstract: Objective To explore the injury mechanism of rat renal tubular epithelial cell (NRK-52E) induced by high glucose by analyzing the alteration of endogenous metabolites using liquid chromatography tandem with mass spectrometry (LC-MS) metabolomics. Methods NRK-52E cell that has been cultured for 12 h in normal condition were randomly divided into low glucose group (LG, 5.56 mmol/L, n=6) and high glucose group (HG, 25 mmol/L, n=6). After being cultured for 48 h, the metabolites from NRK-52E cell of LG and HG group were analyzed by LC-MS and the cell morphology was observed by optical microscope . The principal component analysis (PCA) and partial least squares to latent structure-discriminant analysis (PLS-DA) were performed using Mass Profile Professional (MPP) software to discriminant potential biomarkers. The structures of potential biomarkers were identified using METLIN data. Results The morphology of NRK-52E cells showed that the high- glucose environment was cytotoxic to NRK-52E cells. The results of metabolomics showed that the levels of leucine, hypoxanthine, ceramide (d18:0/12:0, d20:0/16:0, d18:0/16:0, t18:0/16:0, d18:0/14:0), p hosphatidylserine (16:0/16:0, 14:0/12:0, 20:0/0:0), phosphatidylinositol (17:2/20:2), lyso-phosphatidylethanolamine (0:0/20:5, 0:0/20:2) and phosphatidylethanolamine (16:0/0:0) in NRK-52E cells of HG group were significantly increased when comparing with the LG group . Conclusion The injury of NRK-52E induced by high glucose are closely with the metabolism of amino acid, purine and phospholipid in the cells

       

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